Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2020 Jun 17;40:101214. doi: 10.1016/j.ctcp.2020.101214

A narrative literature review on traditional medicine options for treatment of corona virus disease 2019 (COVID-19)

Amir Mirzaie a, Mehrdad Halaji b, Farhad Safarpoor Dehkordi c, Reza Ranjbar a,, Hassan Noorbazargan d
PMCID: PMC7831809  PMID: 32891290

Abstract

Coronavirus disease 2019 (COVID-19) as a life-threatening disease is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that is accounted as global public health concern. Treatment of COVID-19 is primarily supportive and the role of antiviral agents is yet to be established. However, there are no specific anti-COVID-19 drugs and vaccine until now. This review focuses on traditional medicine such as medicinal plant extracts as promising approaches against COVID-19. Chinese, Indian and Iranian traditional medicine, suggests some herbs for prevention, treatment and rehabilitation of the diseases including COVID-19. Although, inhibition of viral replication is considered as general mechanism of herbal extracts, however some studies demonstrated that traditional herbal extracts can interact with key viral proteins which are associated with virus virulence. Chinese, Indian and Iranian traditional medicine, suggests some herbs for prevention, treatment and rehabilitation of the diseases including COVID-19. However the beneficial effects of these traditional medicines and their clinical trials remained to be known. Herein, we reviewed the latest updates on traditional medicines proposed for treatment of COVID-19.

Keywords: COVID-19, Coronavirus, Traditional medicines, Treatment

Highlights

  • Research evidence on traditional medicine against COVID-19 remained to be known.

  • This is an updated review to comprehensively evaluate the importance of traditional medicine on treatment of COVID-19.

  • The roles of Chinese, Indian and Iranian herbal medicine in combination with western medicine to recovery of COVID-19.

1. Introduction

Coronaviruses are enveloped single-stranded RNA positive sense viruses with an average size between 60 nm and 140 nm in diameter with a crown-like shape under electron microscopy [1]. The novel coronavirus (nCoV-2019), coronavirus disease 2019 [2] or Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2) is being first reported from Wuhan of Hubei Province of China before being detected in other countries [3]. The first case was reported in December 2019, then, five patients were hospitalized with acute respiratory signs that one of these patients died [4]. On 30 January 2020, the World Health Organization [5] declared a public health emergency of international concern for COVID-19 [6]. Although the WHO said: "There is no specific medicine recommended to prevent or treat the novel coronavirus till now. The WHO, European Medicines Agency [7], US Food and Drug Administration (FDA) and the Chinese government and drug manufacturers are coordinating with researchers and industrials to accelerate the development of new drugs for COVID-19 [8].

Natural products and their derivatives have potential activities in the treatment of viral infections [9,10]. Until now, several herbal extracts or their derivatives have shown potential antiviral efficacy. However, there are no adequate studies on the development of anti-COVID-19 agents from herbal extracts [2]. Such herbal extracts are important to prevent and combat COVID-19. Generally, Chinese Medicine (CM) has suggested great clinical experiences, effective and applicable herbal formulas on the inhibition and treatment of respiratory diseases [11]. Chinese Traditional Medicine (CTM) suggests the Chinese medicinal herbs based on patients symptoms according to the Chinese diagnostic patterns. CTM could be an alternative strategy for the prevention of COVID-19 in high-risk populations [12]. However, some studies showed that Chinese herbal formula may be associated with viral replication and blocking of the viral proliferation [13]. Chinese herbal medicine with western medicine have suggested the regimen which decrease viral complications. On 24 January 2020, the first patient with symptoms of COVID-19 pneumonia, was recovered from hospital after treatment with traditional Chinese herbal medicine [14]. On 27 January 2020, the Chinses national health office issued diagnosis and treatment of COVID-19 pneumoniae. Although, traditional Chinese herbal medicine in being applied for COVID-19 pneumonia, its effectiveness remains uncertainly [15].

Indian medicinal plants are a promising field for treatment of several diseases [16]. Ayurveda and Siddha practices originated in India and are still widely used among the Indian population. In addition, identification of phyto-components of medicinal plants may be helpful for alleviate the infection. Hence, Indian medicinal plants can be considered as new option for their role to overcome viral transmission [17]. At this time, all of countries have to join hands together to fight COVID-19 by practicing hand-hygiene and social distancing. In the current study, we reviewed and summarized the published data about traditional herbal medicine for possible treatment of COVID-19.

2. General virology and epidemiological characteristics of COVID-19

Coronaviruses cause a lot of disorders, including respiratory, enteric, hepatic and neurologic disease [4]. The SARS-CoV-2 genome has approximately 29 kb size which encodes a large four structural proteins and five accessory proteins including ORF3a, ORF6, ORF7, OR8 and ORF9 [3]. The SARS-CoV-2 can enter to respiratory cells via the angiotensin-converting enzyme 2 (ACE-2) receptor [18]. After binding of SARS-CoV-2 to angiotensin-converting enzyme 2 (ACE-2), the viruses firstly infects lower airways and induced the inflammatory cytokines [19]. The primary cell disruption mechanism is the extreme activation of cytokine [20]. The activated immune cells via virus have led to cytokine and chemokine secretion into pulmonary vascular endothelial cells. Among inflammatory cytokines, IL-12, IL-7, IL-10, GCSF, MCP1 and TNF-α produced more in comparison to other cytokines [21]. Several studies showed that some of the patients who were admitted to the intensive care unit revealed a high level of pro-inflammatory cytokines such as IL-12, IL-17, IL-10, GCSF and TNF-α in their blood samples [22].

Generally, there are three routes for transmission of COVID-19: 1) aerosol transmission, 2) droplets transmission, and 3) contact transmission [23]. Study of a large number infected patients found out that the main transmission route of SARS-CoV-2 is person-person contact [24]. Moreover, it appears that the fomites can be as second suspected source of infection [5]. Recently, Chinese researchers reported that COVID-19 can be detected in the patient's feces, showing a possible fecal-oral transmission [25].

For patients with suspected infection, some molecular tests such as Real-Time Polymerase Chain Reaction (RT-PCR) and next-generation sequencing was suggested for viral detection and characterization. The most common clinical samples is used for detection of SARS-CoV-2 are throat swab, secretion of lower respiratory tract and sputum. In addition, CT imaging can be useful for detection of SARS-CoV-2 and several studies revealed that CT is often positive in patients with SARS-CoV-2 which have cough, fever and fatigue. In patients with severe disease, bilateral pulmonary parenchymal grounded-glass shadow and nodules is observed [26].

3. Prevention and treatment options

3.1. Conventional treatment candidates for COVID-19

To date, there are no specific antiviral agents or vaccines against COVID-19 infection and only the treatment method is supportive and symptomatic. The common principles are maintaining hydration, nutrition condition and controlling the fever [4]. In patients who suffering from hypoxia, supply oxygen via mechanical ventilation, high flow nasal cannula and face mask in an essential procedures. There are some anti-viral drugs that can be used as anti- SARS-CoV-2 agents including interferon-alpha (IFNα), Lopinavir/ritonavir (Kaletra), Ribavirin, Chloroquine, Arbidol (umifenovir) and Remdesivir [27,28]. IFNα belongs to type 1 IFNs which plays an important role in host resistance to viral infection. Inducing of innate and adaptive immune responses by IFNα can inhibit the viral infection via interfering with the replication process. Experimental data and in-vivo analysis showed that IFNα inhibits the replication of SARS-CoV in vitro and cynomolgus monkeys. So, IFNα can be considered as a drug candidate for COVID-19 therapy [29].

Kaletra was used as a protease inhibitor for human immunodeficiency virus [16] which interferes with viral replication. Several molecular studies indicated that Kaletra can bind to endopeptidase C30 of SARS-CoV-2 protease. In addition, some researchers showed that the use of Kaletra alone or in combination with other antiviral drugs can improve the treatment efficacy in patients with SARS or MERS. As a result, Kaletra may have an anti- SARS-CoV-2 effect but further studies are needed to confirm this possibility [30]. Ribavirin as a nucleoside analogue can interfere with guanosine triphosphate (GTP) synthesis in both DNA and RNA viruses. In Hong Kong, ribavirin was extensively used to treat SARS cases. Thus, ribavirin could be considered as anti- SARS-CoV-2 drug candidate. Chloroquine is one of another drug used for malaria and autoimmune diseases. Recently, chloroquine has been used as an antiviral agent and it can effectively inhibit SARS-CoV-2 virus in in vitro [31].

Arbidol is an anti-influenza drug that is used in Russia and China and some studies showed that Arbidol and Arbidol mesylate had potential anti- SARS-CoV-2 in in-vitro. In addition, many randomized clinical trials are being performed about Arbidol efficiency on COVID-19 infection in China [19]. Remdesivir (GS-5734) as a nucleoside analogue was shown to inhibit SARS-CoV and MERS-CoV in in-vitro [32]. Remdesivir in cells and tissues convert to an active form that inhibits viral RNA dependent RNA polymerase in the early phase of infection. Remdesivir was developed for the treatment of Ebola hemorrhagic fever for the first time. In the USA, the first case of SARS-CoV-2 infection was treated via remdesivir injection. However, randomized controlled trials are needed for the safety and efficacy of remdesivir.

In conclusion, the mentioned anti-viral drugs may be promising treatment choices for treatment of COVID-19 infection. However, the side effects of drugs, including diarrhea, nausea, vomiting and interaction with other therapeutic drugs should be considered [33]. Remdesivir is an anti-viral drug undergoing phase 3 clinical trials for treatment of patients with COVID-19 infection. Clinical trials are studying remdesivir with a loading dose of 200 mg intravenously followed by 100 mg intravenously daily for 5–10 days in adult patients. However, it showed side effects in some patients including nausea, vomiting, gastroparesis, or rectal bleeding. Moreover, these patients had more ratio of aminotransferase levels occurring 1–5 days after initiating remdesivir [34]. Favipiravir is an RNA-dependent RNA polymerase inhibitor similar to remdesivir which is developed by Toyama Chemical (Division of Fujifilm, Japan). After the administration of favipiravir, viral replication can be reduced and its specific drug for Influenza and there is less clinical study support for treatment of COVID-19. In March 2020, favipiravir was approved in China as the first choice for COVID-19 therapy. However, the clinical trial showed some side effects [35]. Chloroquine derivatives including chloroquine phosphate and hydroxychloroquine, have been used for the treatment of malaria in the 1900s for the first time. In addition, chloroquine analogues have immunomodulatory effects which can be used for autoimmune diseases such as lupus erythematosus and rheumatoid arthritis. Recently, hydroxychloroquine has also been studied against SARS-CoV-2 in in-vitro. The anti-viral and anti-inflammatory activities of chloroquine are practical choice in preventing COVID-19-related pneumonia [36]. Boosting the immune system is an alternative way for treating the COVID-19 patients. Interferons can inhibit the replication of the virus via inducing the innate and adaptive immune response. Many clinical trial studies indicated that interferon alpha can be efficient for treatment of SARS and MERS-CoV infected patients. Based on studies findings, interferon suggests for treatment of COVID-19 infection. In addition, thymosin alpha-1 (Ta1) is one immune booster for infected patients with SARS and it can prevent the spread of infection. So, the administration of Ta1 can be used as drug candidate for COVID-19 treatment [37,38].

There are some reports regarding immunotherapy of viral infection using antiviral antibodies (IgG, IgA, IgM, IgE and IgD) which recovered from plasma of patients. Earlier, plasma therapy has been used for poliomyelitis, influenza A (H5N1) and Ebola. For COVID-19 treatment, immune therapy can be achieved by plasma from COVID-19 patients [39]. Some reports showed that plasma therapy of SARS patients can decrease viral load from 105 copies/mL to near zero after 24 h plasma therapy. So, plasma therapy can be considered a promising achievement for COVID-19 treatment. In addition, monoclonal antibodies are another drug candidate for viral therapy. Monoclonal antibodies against inflammatory cytokines or innate immunity responses is another immunotherapy achievement. Prior research revealed that monoclonal antibody can bind to SARS-CoV spike protein which can inhibit the virus cell entry. One of the promising monoclonal antibodies can be CR3022 due to its binding affinity to virus for the treatment of COVID-19 [40]. Monoclonal antibodies against IL-6 can be useful to decrease the cytokine storm. Tocilizumab is a monoclonal antibody against IL-6 receptor which is approved by the FDA. A report of 21 COVID-19 infected patients who received 400 mg showed a decrease in clinical manifestation in 91% of patients. Sarilumab is another IL-6 receptor antagonist which is approved RA and is being studied in phase 2/3 clinical trial. There are monoclonal antibodies such as bevacizumab, fingolimod and eculizumab which is in a clinical trial in China [41] (see Table 1).

Table 1.

Ongoing clinical trial drugs listed for treatment COVID-19.

Clinical trial phase Drug formulation Number of Clinical samples Ref.
III, IV CD24Fc 230 participants with COVID-19 [85]
III, IV ASC-09 + ritonavir 160 participants with COVID-19 [86]
III, IV Dapagliflozin 900 participants with COVID-19 [87]
III, IV Lopinavir/ritonavir without or with Rebif 3100 participants with COVID-19 [88]
III, IV Tocilizumab 400 participants with COVID-19 [89]
III, IV Sarilumab 400 participants with COVID-19 [90]
II Azithromycin 600 participants with COVID-19 [91]
III Lenzilumab 238 participants with COVID-19 [92]
III, IV favipiravir 40 participants with COVID-19 [93]
N/A Chloroquine 10000 patients with COVID-19 [94]
N/A CTM + lopinavirritonavir,
IFN-alpha
150 samples positive with COVID-19 [53]
I Recombinant human IFN- a2b 328 samples positive with COVID-19 [94]
II Thalidomide 100 Pneumonia cases caused by COVID-19 [95]
II Vitamin C 140 severe participants caused by COVID-19 [96]
II Methylprednisolone 80 SARS-CoV-2 infected individuals [8]
II Thalidomide 100 Pneumonia cases caused by COVID-19 [95]
II Fingolimod 30 samples positive for 2019-nCoV [94]
II/III Bevacizumab 20 infected participants with severe
2019-nCoV
[97]
III Oseltamivir, favipiravir, and chloroquine 80 SARS-CoV-2 positive samples [98]
III Pirfenidone 294 severe
COVID-19 participants
[94]
III Remdesivir 308 patients with Moderate COVID-19 [94]
III Darunavir + cobicistat 30 Pneumonia cases caused by COVID-19 [98]
III Remdesivir 452 severe infected persons [99]
III Hydroxychloroquine 30 COVID-19 infected patients [84]
IV Arbidol 380 individuals caused by COVID-19 [94]
IV Arbidol/lopinavir-ritonavir 125 COVID-19 patients [100]
IV Carrimycin/lopinavir-ritonavir/Arbidol/chloroquine phosphate 520 COVID-19 infected patients [29]

In Italy, a great study done by the Istituto Nazionale Tumori, Fondazione Pascale di Napoli is focused on the use of tolicizumab. It is a humanized IgG1 monoclonal antibody, directed against the IL-6 receptor and commonly used in the treatment of rheumatoid arthritis. In some countries, there are no options for treatment and prevention such as vaccine or specific coronavirus drugs, so, convalescent plasma therapy is an alternative strategy to decrease the course of infection in hospitalized patients [42]. The studies showed that convalescent plasma therapy has more efficacy in patients with SARS infection. In 2009, Hung et al., showed that in infected patients with Influenza H1N1 which received the convalescent plasma had low rate of mortality [43]. In addition, the persons who recovered from COVID-19, their plasma include specific antibodies against COVID-19 and it could be useful to disease prevention. Moreover, the antibodies can reduce the viral replication in the acute phase of infection and help to clear the virus and recovery [44]. Overall, in the first week of most viral infection, viremia occur and it should be more useful to a collection of convalescent plasma. Finally, plasma globulin could be collected from COVID-19 patients and it used to recovery patients [45]. However, randomized double-blinded clinical trials with large sample sizes should be used as the standard to determine whether antiviral drugs could be used in clinical practice [46,47]. Recently, many drugs formulates are in clinical trials and they can be considered as new drug candidates for SARS-COV-2 (Table 2 ). After search the terms of COVID-19 or SARS-COV-2 on clinical-trials.gov resulted in 291 trials related to COVID-19 as of April 2, 2020. Among 291 clinical trials, around 109 trials included pharmacological therapy for treatment of COVID-19 in adult persons. Researcher used previously antiviral agents against SARS and MERS as drug candidates for COVID-19 [48].

Table 2.

Herbal formula used for the treatment of SARS-CoV infection.

Name of herbal formula List of compound Ref.
Ma Xing Shi Gan Decoction Semen armeniacae amarum (ku xing ren), Glycyrrhizae radix preparata (gan cao), Gypsum fibrosum (shi gao), Ephedrae herba (ma huang) [94]
Da Yuan Yin decoction Houpo (Magnoliae officinalis cortex), Binlang (Arecae semen), Caoguo
(Tsaoko fructus), Huangqin (Scutellariae radix), Gancao (Glycyrrhizae raadix et rhizoma), Zhimu (Anemarrhenae rhizoma), Shaoyao (Dioscoreae rhizoma)
[101]
Qing Fei Pai Du decoction Shigao (Gypsum fibrosum), Mahuang
(Ephedrae herba), Banxia
(Pinelliae rhizoma), Shengjiang (Zingiberis rhizoma recens), Zhishi (Aurantii fructus immaturus)
[11]
Sang Ju Yin Sang Ju Yin [made with chrysanthemum, mulberry leaf, and 6 other herbs] [103]
Yu Ping Feng San Astragali radix, Astragalus membranaceus, Atractylodes macrocephala, and Saposhnikoviae Radix [102]

3.2. Traditional herbal medicine

3.2.1. Botanical claims

A series of herbal and fruit extract was reported as claims to remedy virus infections. Sri Lankan herbal drink is used for inhibition of viral infections such as SARS-CoV-2 which reduces the fever symptoms. Some studies demonstrated that Andrographis paniculata boost the immune system and it can decrease the symptoms of coronavirus. Also, Tinospora crispa (makabuhay) was used as an antiviral drug candidate for coronavirus where used as an eye drop. Drinking lemon juice in warm water has been claimed to prevent COVID-19 disease by elevating the vitamin C levels. However, WHO reported that there is no evidence for this claim but recommended consuming fresh fruits. In addition, there are some claims about banana, garlic, Juice of bittergourd, turmeric and Azadirachta indica to prevent COVID-19 but there is no supporting data [49].

3.2.2. Traditional herbs

Traditional herbs from different habitats and geographical locations can be considered as new candidate combination for treatment of viral infections such as SARS-CoV. Preliminary studies have shown that concanavalin A, a phytoagglutinin in jack beans (Canavalia ensiformis) can binds to glycosylated membrane proteins and prevent the target cell recognition and virus entry. However, subsequent studies showed that its intense hepatotoxicity restrict the therapeutic utility [50]. More studies showed that some medicinal plants extract including Lycoris radiata, Artemisia annua, Pyrrosia lingua, and Lindera aggregata exerted anti-SARS-CoV at 2.4–88.2 μg/mL [51]. Some reports showed that lycorine, an active phyto-compound from Lycoris radiate inhibited SARS‐CoV with effective concentration of 15.7 nM [52]. Moreover, high toxicity of lycorine against VERO E6 and HepG2 cell lines makes it as good drug candidate for anti-cancer activity. Lau et al. demonstrated that the aqueous extract of Houttuynia cordata can inhibit two efficient protein namely chymotrypsin‐like protease (3CLpro) and RdRp in SARS‐CoV [53]. In addition, the H. cordata extract can enhanced the CD4+ and CD8+ cell count in in vitro tests in animals showing its immune-stimulatory effect that can considered as important feature for inhibition of viral replication [54]. Similarly, some medicinal plant extracts including Rheum officinale, Polygonum multiflorum, emodin and some other active components of these herbs were found to inhibit the bindings of SARS‐CoV (S) spike protein to ACE2 with IC50 values between 1 and 10 μg/mL, and 200 μM for emodin [55].

Methanolic extract of Cibotium barometz and Dioscorea batatas showed inhibitory activity against SARS‐CoV 3CLpro with IC50 values of 39 and 44 μg/mL, respectively [56]. In addition, Anthemis hyalina, Nigella sativa, and Citrus sinensis extracts exhibited the inhibitory effects on MHV‐A59 (mouse hepatitis virus–A59) with priority of A. hyaline extract. Its mechanisms depends on down-regulation of TRP gene expression and increase the level of intracellular calcium level [57].

Recent published data showed that plant alkaloids namely tetrandrine, fangchinoline, and cepharanthine can significantly reduce the cell death due to viral infection in MRC-5 human lung cells. In addition, some active phyto-constituents including ten diterpenes, two sesquiterpenes, two triterpenes, five lignans, and curcumin can inhibit the SARS‐CoV. The isolated Kazinol A, kazinol B, kazinol F, and kazinol J from Broussonetia papyrifera inhibit SARS‐CoV 3CLpro. Sivestrol, an active phyto-component of Aglaia foveolata has potent in vitro cytotoxicity against human cancer cell lines. Moreover, this constituent inhibit the HCoV‐229E mRNA translation with IC50 value of 40 nM [58]. On the other hand, ferruginol, a phenolic compound extracted from the redwood Sequoia sempervirens, betulinic acid, hinokinin, savinin, and curcumin showed anti-SARS‐CoV replication activity. In addition, ouabain decreased significantly the viral RNA copies number. There are some reports in regarding to Tylophorine extracted from Tylophora indica as inhibitor of viral replication in from CoV‐infected swine testicular cells [59].

Chinese traditional herbal medicine (CTM) played a key role and has long background in the treatment and control of several epidemic diseases from plague to SARS. CTM was used for the treatment of SARS-CoV outbreak in 2002. During this epidemic, CTM was reported to have favored effects to control SARS disease. Lau and co-workers used CTM herbal extract namely Sang Ju Yin plus Yu Ping Feng San for 1063 volunteers including 926 hospital workers and 37 laboratory technicians working in high-risk virus laboratories. The results of this study showed that none of CTM users were infected by the virus. It was suggested that Sang Ju Yin plus Yu Ping Feng San could regulate T cells for boosting the immune system [60]. In addition, some studies demonstrated that supplementary treatment with CTM could be useful for the improvement of symptoms. Leung et al. studied 90 peer-reviewed articles and concluded that combination of CTM used combination with conventional treatment had some positive effects, including diminished fever, faster clearance of chest infection and other symptoms. However, such positive effect of CTM is not conclusive and more clinical studies are needed [11].

Moreover, some flavonoids such as herbacetin, isobavaschalcone, quercetin 3‐β‐D‐glucoside, and helichrysetin have inhibitory activity against MERS‐CoV 3CL protease. Findings of many studies indicated that after administration of some herb-derived constituents such as sinigrin, indigo, aloe-emodin, hesperetin, quercetin, epigallocatechin gallate, gallocatechin gallate, herbacetin, rhoifolin and pectolinarin, the activity of the SARS 3CLpro could be blocked. It was reported that the extracts of Kang Du Bu Fei Tang, Sinomenium acutum, Coriolus versicolor and Ganoderma lucidum inhibited SARS-CoV RNA-dependent RNA polymerase. Emodin extracted from genus Rheum and Polygonum, baicalin from in Scutellaria baicalensis, nicotianamine from foodstuff (especially “soybean ACE2 inhibitor (ACE2iSB), scutellarin, tetra-O-galloyl-β-d-glucose (TGG) from Galla chinensis and luteolin from Veronicalina riifolia significantly inhibited the interaction of SARS-CoV S-protein and ACE2 [61]. As well as, inhibition of the 3a ion channel by emodin or kaempferol derivatives-juglanin could significantly block the viral release from the infected cells. Saikosaponins, glycyrrhizin, quercetin and TSL-1 originated from Toona sinensis Roem had potent anti-SARS-CoV effects by inhibition of viral cellular entry, adsorption, and penetration [62,63].

Because of the similarity between in SARS-CoV-2 and SARS-CoV in the context of virology, genomics and pathogenesis and successes of CTM for controlling of SARA in 2002–2003, CTM could be an alternative choice instance of chemical drugs for prevention of SARS-CoV-2 outbreak. After outbreak the COVID-19, Chinese herbal medicine treatment program, allocates expert Scientifics in the field of CTM to discover and formulate a traditional prescription for controlling COVID-19. The first case of COVID -19 cured and discharged from hospital by prescription of CTM was reported on 24 January 2020 in Beijing [64].

According to the evaluation of the cases infected with COVID-19 who treated by CTM, the results showed that the time of disappearing of clinical symptoms, staying of patient in hospital decreased by 2, 1.7, 2.2 days, respectively. CTM alone or in combination of western medicine like antibiotic or antiviral drugs regimen could be effective for treatment or prevention of COVID-19. China reported traditional medicine to treatment of patients with COVID-19 and Chinese researchers showed that 91.6% of patients in Hubei province and 92.4% of patients nationwide have been treated with traditional medicine. The studies showed that some formulas can be effective in treating the disease. Jimhua Qinggan granule is one of herbal formula which consists 12 herbal components including honeysuckle, mint and licorice. It can decrease the body temperature and remove toxic substances from lungs. This formula has significant effects in treating the patients with moderate influenza H1N1 and can increase the recovery rate of lymphocytes and white blood cells. Similar experiments indicated that the patients who received the Jimhua Qinggan granule, two days earlier recovered compared to those didn't receive it. As, the recovery time in these patients (patients who took Jimhua Qinggan granule) was eigth days compared to other groups (10.3 days) [64]. Another herbal formula is Lianhua Qingwen capsule/granule which is very common herbal extract for treatment of cold and flu [65].

In another study was shown that Sang Ju Yin plus Yu Ping Feng San extract was used for treatment of 1063 patients of SARS in 2003 that showed a significant effect. Also, these herbs could increase host defense through modulation of T cells. Glycyrrhizin in Chinese medicine is used as an inhibition factor for SARS-CoV in vitro and its high dose has been used in clinical trials. Some reports showed that glycyrrhizin could have the ability to bind ACE2 as anti- SARS-CoV-2 drug candidate. In traditional Chinese medicine, Hesperetin, a well-known flavonoid in citrus fruits is used as 3C-like protease suppressor for SARS-CoV in cell culture experiments. In addition, Hesperetin can bind to ACE2 and inhibit it [66]. In Chinese medicine, Baicalin, flavone extract from Scutellaria baicalensis, was used as anti-viral agent against SARS-CoV. In a recent study, a new drug known as EIDD-2801 discovered to treat COVID-19 infection. The result shows that EIDD-2801 significantly reduces virus replication in mouse model. EIDD-2801 is a ribonucleoside analog with antiviral activity against influenza, Ebola and CoV, can be taken as pill reverse of remdesivir. Recently, many drugs formulates are in clinical trials and they can be considered as new drug candidates for COVID-19 (Table 2) [67]. According to Chinese traditional science, food is categorized ying (cool) or yang (hot). It was believed that SARS infected yang (hot) body system because of that it was recommended people to consume liang (cool) foods. Kim et al. revealed that Phellodendron cortex, Sophora subprostrata Radix, Cimicifuga Rhizome, Coptidis rhizometreated could inhibit expression S and N protein and RNA synthesis in coronavirus. It is also virus reported that the virus assembly and release might be affected by Coptidis Rhizome and Meliae cortex [68].

Traditional medicine especially CTM has shown significant and effective therapies for influenza A H1N1, H7N9, Ebola and SARS-CoV. Based on the beliefs of ancient Chinese traditional medicine man is a part of nature and environment is pivotal factor in pathogenesis of diseases like the plaque. In the case of SARS-CoV-2 they think that this virus characteristic depends on the climatic condition of Wuhan. According to CTM reference “Standard Therapy of COVID-19” Ma Xin Gan Shi decoction with Da Yuan Yin extract could be effective to decrease the symptoms in COVID-19 patients. The Ma Xin Gan Shi and Da Yun Yin decoction were evaluated for the treatment of SARS-CoV [61]. In Table 3 the detailed compound of these extracts are listed. According to related study the five compounds: 7-methoxy-2-methyl isoflavone, formononetin, quercetin, baicalein and kaempferol could be interfering with SARS-CoV 3CL protease. Another study indicated that Qing Fei Pai Du decoction [69] (Table 3), that is a modification of Ma Xing Gan Shi, She Gan Ma Huang, Xiao Chai Hu, and Wu Ling San decoctions, is not effective in effective in treating COVID-19. Huo Xiang Zheng Qi capsule (derived from Tai Ping Hui Min He Ji Ju Fang) which has patent medicine can be effective for treatment of the gastrointestinal symptoms of COVID-19 [61]. Also Lian Hua Qing Wen capsules and Fang Feng Tong Sheng pills can decrease the severity of symptoms (fever, fatigue and Cough) related to COVID-19, also Lian Hua Qing Wen capsule can be effective for SARS, MERS and influenza. Numerous studies showed promising results for prevention and treatment of COVID-19 by CTM. Yao et al. and Lu et al. demonstrated that the most of confirmed COVID-19 infected patients had relieved in their symptoms such as fever and cough [70]. Qing Fei Pai Du Tang is another herbal formulate which is used in China for treatment of 214 COVID-19 patients. After administration of this formula, the symptoms of the most patients (≥60%) were significantly improved and 130 patients were completely cured [44].

Table 3.

Recently TCM herbal medicine research for treatment of SARS-CoV-2 infection.

Clinical trial phases TCM herbal medicine Number of tested samples Form/Rout of administration Ref.
N/A Gu Biao Jie Du Ling 200 COVID-19 samples [67]
N/A Tan Re Qing 72 COVID-19 samples Capsules [67]
IV Tan Re Qing 72 COVID-19 samples Injection [84]
IV Lian Hua Qing Wen 400 COVID-19 samples Capsule/Granule [67]
N/A Jin Yin Hua Tang 110 COVID-19 samples [14]
IV Shuang Huang Lian 400 COVID-19 samples Oral Liquid [67]
IV Xi Yan Ping 348 COVID-19 samples Injection [81]
IV Shen Fu 300 COVID-19 samples Injection [67]
IV Jing Yin Granule 300 COVID-19 samples Granules [67]
IV Shen Qi Fu Zheng 160 COVID-19 samples Injection [104]
IV Kang Bing Du 160 COVID-19 samples Granules [60]
IV Ke Su Ting Syrup
/Ke Qing
72 COVID-19 samples Capsule [67]

Recently it has been reported that about 60107 cases were treated by CTM. According to treatment results reported from China qingfei paidu decoction (QPD), gancaoganjiang decoction, sheganmahuang decoction and qingfei touxie fuzheng recipe could be effective for diagnosis and treatment of SARS-CoV-2 (93). The reported have shown that 701 patients cured by QPD which 130 persons were treated and sent back to the home, in 51 and 268 cases clinical signs were lost and improved respectively, and in 212 patients the symptoms were stable. The rate of COVID-19 treatment by QPD is more than 90%. According to molecular interaction analysis it has been shown that patchouli alcohol, ergosterol and shionone provided new drug choice for treatment of SARS-CoV-2. SHL (Shuang huang lian oral liquid) consists of three Chinese plants including honeysuckle, forsythia, and Scutellaria baicalensis and because of cost and no serious side effect used for treatment of sore throat, cough with fever and cold. In a study conducted by Ni et al., SHL combined with other treatment (Intravenous immunoglobulin, dexamethasone, antibiotics, and antivirus drugs) were used for treatment of COVID-19. The results showed that this regimen prescription could resolve the symptoms and improvement without side effects [47].

Wang et al. suggested that Shen Fu Injection could decrease the level of IL-1β, TNF-α, IL-8, IL-10 and some related inflammatory cytokines. The results of this study showed that Shen Fu Injection could inhibit the lung inflammation [71]. An in vitro study indicated that Shuang Huang Lian Oral Liquid had the inhibitory effect on COVID-19. However, its clinical efficacy and safety for the treatment of COVID-19 patients has not been studied. Respiratory Detox Shot (RDS), is a kind of CTM which contain nine CTM substances including Schizonepetae Herba (Jingjie), Lonicerae Japonicae Flos (Jinyinhua), Forsythiae Fructus (Lianqiao), Scrophulariae Radix (Xuanshen), Gleditsiae Spina (Zaojiaoci), Armeniacae Semen Amarum (Kuxingren), Nidus Vespae (Fengfang), Glycyrrhizae Radix et Rhizoma (Gancao) and Ginseng Radix et Rhizoma (Renshen). These herbal ingredients has therapeutic benefits for respiratory tract infections especially COVID-19 [62,63].

Behind, previous studies have revealed that these herbal products effectively prevented release of inflammatory cytokines (TNF-α, IL-1β, a nd I L-6) in lipopolysaccharide-stimulated murine alveolar macrophages. Consequently, CTM may be effective in the treatment of severe patients with the ability to prevent cytokine storm and its disturbing consequences [67].

Indian traditional medicine in one of the oldest treatments in human history and Ayurveda, Siddha, Unani and Yoga, Naturopathy and Homeopathy plays an important role for treating the various diseases [72]. Approximately, 2500 medicinal plant based formulation have been used in Indian traditional medicine. Since a lot of Indian medicinal plants showed antiviral, anti-oxidant and anti-cancer activities that it may be important to consider their precise activities [72]. However, several clinical trials must be done to confirm its activity [72]. There are many studies about anti-coronavirus activity using medicinal plants in India. In one study, it was shown the medicinal plants including Indigofera tinctoria (AO), Vitex trifolia, Gymnema sylvestre, Abutilon indicum, Leucas aspera, Cassia alata, Sphaeranthus indicus, Clitoriaternatea, Clerodendruminerme Gaertn, Pergulariadaemi and Evolvulus alsinoides in Tamil Nadu has anti-mouse coronavirus activity [73]. Among them, Vitex trifolia and Sphaeranthus indicus have been shown to decrease the inflammatory cytokine level using the NF-kB pathway, an important pathway in respiratory distress in SARS-CoV [74]. In addition, Clitoria ternatea has been found as ADAM17 metalloproteinase inhibitor which is involved in ACR shredding. Some studies have shown that the Glycyrrhiza glabra and Allium sativum have inhibitory effect on SARS-CoV replication and then they can be considered as a promising drug candidate for COVID-19 [75]. Clerodendrum inerme Gaertn is another medicinal herb which has been found to have viral ribosome inhibitory effect and this can be further studied for its ability as drug candidate for COVID-19 protein translation. Moreover, Coriandrum sativum, Boerhaavia diffusa, Cynara scolymus, Coscinium fenestratum, Punicagranatum Cassia occidentalis and Embeliaribes have inhibitory effects on ACE and can be used as potential anti-COVID-19 drug candidate [76]. These medicinal plants need to be investigated more for their potential effect on SARS-CoV-2 entry to target cells. Some medicinal plants such as Acacia nilotica, Eugenia jambolana and Euphorbia granulate have also shown inhibitory effect on HIV protease and these plants can be considered as drug candidate for COVID-19 [77]. Some plants such as Ocimum sanctum, Ocimumkilim and scharicum, Solanum nigrum and Vitex negundo have inhibitory effect on reverse transcriptase of HIV and can be investigated for SARS-CoV-2 [78]. Ganjhu et al. reported that the Sambucus ebulus has inhibitory effect on virus envelope [79]. In conclusion, more studies are needed to perform for Indian medicinal plants in order to the design and development of drug specific to COVID-19 [79].

As mentioned earlier, COVID-19 binds to ACE2 receptor to enter the host lung cells. Ziai and Heidari studied the 20 herbal extracts and found that the Cerasus avium (L.) Moench, Alcea digitata (Boiss.) Alef, and Rubia tinctorum L, Citrus aurantium L.; Berberis integerrima Bge; Peganum harmala L.and Allium sativum L had ACE inhibitory effects. Therefore, these herbals extracts or other plant extracts with similar mechanisms may be suggested as new strategies for the treatment of COVID-19 [80]. It should be mentioned that ACE inhibitors can increase the expression of ACE receptor and may increase the susceptibility of COVID-19 infection. However, the persons who are treated with ACE inhibitors must be excluded from these herbal medicines [79,81]. In addition, WHO recognizes that medicinal plants such as Aretmisia annua are being considered as possible treatment for COVID-19 and the efficacy and side effects must be examined [2,82]. Thus, it can be suggested the Iranian type of A. annua can be used as drug candidate for treatment of COVID-19. In addition, four Iranian companies have launched studies to make herbal medicine for the treatment of COVID-19. However, the clinical tests have begun since March 5, 2020 and after success in the clinical tests, the products should be confirmed by the food and drug organization [14,83,84].

4. Conclusion

With the appearance of COVID-19 outbreak many scientific researchers and clinicians tried to propose effective drugs for eradication of this pandemic disease. Chinese, Indian and Iranian herbal medicine with 1000 years' experience in the prevention of pandemic and endemic infectious diseases are worth learning and providing alternative candidate for controlling of patients with COVID-19 infection. Nowadays, there are not effective treatment for COVID-19, as a result it provides a biggest opportunity to test different plants and decoction for management of this disease. Hopefully, positive results from clinical trial experiments elucidate the positive effects of Chinese, Indian and Iranian herbal medicine alone and in combination with western medicine to recovery of SARS-CoV-2. Our review suggests the further studies on the Chinese, Indian and Iranian herbal medicine would be needed to discover the novel anti-COVID-19 substances useful for eradication of SARS-CoV-2. It highlight the ways that the herbal-based medicines may efficient to overcome COVID-19 fatal infections.

Data availability

Data will be made available upon request.

Declaration of competing interestCOI

The authors declare no conflict of interest.

Acknowledgment

Thanks to guidance and advice from "Clinical Research Development Unit of Baqiyatallah Hospital".

Footnotes

Appendix A

Supplementary data related to this article can be found at https://doi.org/10.1016/j.ctcp.2020.101214.

Appendix A. Supplementary data

The following is the supplementary data related to this article:Multimedia component 1
mmc1.xml (195B, xml)

References

  • 1.Guo Y.-R., Cao Q.-D., Hong Z.-S., Tan Y.-Y., Chen S.-D., Jin H.-J., Tan K.-S., Wang D.-Y., Yan Y. The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreak–an update on the status. Mil. Med. Res. 2020;7(1):1–10. doi: 10.1186/s40779-020-00240-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.C.t.n.N.f.C.F.a.a.N.-a.I.i.C.-T.S.-C.a. ClinicalTrials.gov.
  • 3.Halaji M., Farahani A., Ranjbar R., Heiat M., SAfarpoor Dehkordi F. Emerging coronaviruses: first SARS, second MERS and third SARS-CoV-2: epidemiological updates of COVID-19. Infez Med. 2020;28(1):6–17. 2020. [PubMed] [Google Scholar]
  • 4.Singhal T. A review of coronavirus disease-2019 (COVID-19) Indian J. Pediatr. 2020:1–6. doi: 10.1007/s12098-020-03263-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Numbers S.I., Assessment W.R. Coronavirus disease 2019 (COVID-19) Americas. 2020;10(2):1. [Google Scholar]
  • 6.Wu J.T., Leung K., Leung G.M. Nowcasting and forecasting the potential domestic and international spread of the 2019-nCoV outbreak originating in Wuhan, China: a modelling study. Lancet. 2020;395(10225):689–697. doi: 10.1016/S0140-6736(20)30260-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Prajapat M., Sarma P., Shekhar N., Avti P., Sinha S., Kaur H., Kumar S., Bhattacharyya A., Kumar H., Bansal S. Drug targets for corona virus: a systematic review. Indian J. Pharmacol. 2020;52(1):56. doi: 10.4103/ijp.IJP_115_20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Huang C., Wang Y., Li X., Ren L., Zhao J., Hu Y., Zhang L., Fan G., Xu J., Gu X. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395(10223):497–506. doi: 10.1016/S0140-6736(20)30183-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Denaro M., Smeriglio A., Barreca D., De Francesco C., Occhiuto C., Milano G., Trombetta D. Antiviral activity of plants and their isolated bioactive compounds: an update. Phytother Res. 2020;34(4):742–768. doi: 10.1002/ptr.6575. [DOI] [PubMed] [Google Scholar]
  • 10.Oyero O.G., Toyama M., Mitsuhiro N., Onifade A.A., Hidaka A., Okamoto M., Baba M. Selective inhibition of hepatitis c virus replication by Alpha-zam, a Nigella sativa seed formulation. Afr. J. Tradit., Complementary Altern. Med. 2016;13(6):144–148. doi: 10.21010/ajtcam.v13i6.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Cui H.-T., Li Y.-T., Guo L.-Y., Liu X.-G., Wang L.-S., Jia J.-W., Liao J.-B., Miao J., Zhang Z.-Y., Wang L. Traditional Chinese medicine for treatment of coronavirus disease 2019: a review. Tradit. Med. Res. 2020;5(2):65–73. [Google Scholar]
  • 12.Zumla A., Chan J.F., Azhar E.I., Hui D.S., Yuen K.-Y. Coronaviruses—drug discovery and therapeutic options. Nat. Rev. Drug Discov. 2016;15(5):327. doi: 10.1038/nrd.2015.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Tong X., Li A., Zhang Z., Duan J., Chen X., Hua C., Zhao D., Xu Y., Shi X., Li P. TCM treatment of infectious atypical pneumonia--a report of 16 cases. J. Tradit. Chin. Med. 2004;24(4):266–269. Chung i tsa chih ying wen pan. [PubMed] [Google Scholar]
  • 14.Li X., Zhang X., Ding J., Xu Y., Wei D., Tian Y., Chen W., Huang J., Wen T., Li S. 2014. Comparison between Chinese Herbal Medicines and Conventional Therapy in the Treatment of Severe Hand, Foot, and Mouth Disease: a Randomized Controlled Trial, Evidence-Based Complementary and Alternative Medicine 2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Zhang M.-M., Liu X.-M., He L. Effect of integrated traditional Chinese and Western medicine on SARS: a review of clinical evidence. World J. Gastroenterol.: WJG. 2004;10(23):3500. doi: 10.3748/wjg.v10.i23.3500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Vellingiri B., Jayaramayya K., Iyer M., Narayanasamy A., Govindasamy V., Giridharan B., Ganesan S., Venugopal A., Venkatesan D., Ganesan H. COVID-19: a promising cure for the global panic. Sci. Total Environ. 2020:138277. doi: 10.1016/j.scitotenv.2020.138277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Balachandar V., Mahalaxmi I., Kaavya J., Vivekanandhan G., Ajithkumar S., Arul N., Singaravelu G., Kumar N.S., Devi S.M. COVID-19: emerging protective measures. Eur. Rev. Med. Pharmacol. Sci. 2020;24(6):3422–3425. doi: 10.26355/eurrev_202003_20713. [DOI] [PubMed] [Google Scholar]
  • 18.Jiang F., Deng L., Zhang L., Cai Y., Cheung C.W., Xia Z. Review of the clinical characteristics of coronavirus disease 2019 (COVID-19) J. Gen. Intern. Med. 2020:1–5. doi: 10.1007/s11606-020-05762-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Mohammadpour S., Torshizi Esfahani A., Halaji M., Lak M., Ranjbar R. An updated review of the association of host genetic factors with susceptibility and resistance to COVID-19. J Cell Physiol. 2020:1–6. doi: 10.1002/jcp.29868. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Aldridge M. 2020. Review of the Antiviral Activity and Pharmacology of Monoglycerides and Implications for Treatment of COVID-19. [Google Scholar]
  • 21.Y. Liu, C. Zhang, F. Huang, Y. Yang, F. Wang, J. Yuan, Z. Zhang, Y. Qin, X. Li, D. Zhao, Elevated plasma level of selective cytokines in COVID-19 patients reflect viral load and lung injury. 2020. DOI: 10.31219/osf.io/qdsef. [DOI] [PMC free article] [PubMed]
  • 22.Brogna C. 2020. The" Zero Point" and the Autonomous Nervous System. Reverse Analysis, Syllogism and Genetic. Possible Correlations with the Covid19 Virus. A New Perspective. [Google Scholar]
  • 23.Organization W.H. World Health Organization; 2020. Modes of Transmission of Virus Causing COVID-19: Implications for IPC Precaution Recommendations: Scientific Brief, 27 March 2020. [Google Scholar]
  • 24.Yuen K.-S., Ye Z.-W., Fung S.-Y., Chan C.-P., Jin D.-Y. SARS-CoV-2 and COVID-19: the most important research questions. Cell Biosci. 2020;10(1):1–5. doi: 10.1186/s13578-020-00404-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Hindson J. COVID-19: faecal–oral transmission? Nat. Rev. Gastroenterol. Hepatol. 2020;17(5) doi: 10.1038/s41575-020-0295-7. 259-259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Tahamtan A., Ardebili A. Taylor & Francis; 2020. Real-time RT-PCR in COVID-19 Detection: Issues Affecting the Results. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Li G., Zhao J., Tu Z., Li J., Liu Q., Shi L., Miao Q., Yuan H., Liu X., Long Y. Treating influenza patients of wind-heat affecting Fei syndrome by jinhua qinggan granule: a double-blinded randomized control trial. Chin. J. Integr. Tradit. West. Med. 2013;33(12):1631–1635. Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi. [PubMed] [Google Scholar]
  • 28.Li H., Liu S.-M., Yu X.-H., Tang S.-L., Tang C.-K. Coronavirus disease 2019 (COVID-19): current status and future perspective. Int. J. Antimicrob. Agents. 2020:105951. doi: 10.1016/j.ijantimicag.2020.105951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Cao B., Wang Y., Wen D., Liu W., Wang J., Fan G., Ruan L., Song B., Cai Y., Wei M. A trial of lopinavir–ritonavir in adults hospitalized with severe Covid-19. N. Engl. J. Med. 2020 doi: 10.1056/NEJMoa2001282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Stower H. Lopinavir–ritonavir in severe COVID-19. Nat. Med. 2020;26(4) doi: 10.1038/s41591-020-0849-9. 465-465. [DOI] [PubMed] [Google Scholar]
  • 31.Liu J., Cao R., Xu M., Wang X., Zhang H., Hu H., Li Y., Hu Z., Zhong W., Wang M. Hydroxychloroquine, a less toxic derivative of chloroquine, is effective in inhibiting SARS-CoV-2 infection in vitro. Cell Discov. 2020;6(1):1–4. doi: 10.1038/s41421-020-0156-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Agostini M.L., Andres E.L., Sims A.C., Graham R.L., Sheahan T.P., Lu X., Smith E.C., Case J.B., Feng J.Y., Jordan R. Coronavirus susceptibility to the antiviral remdesivir (GS-5734) is mediated by the viral polymerase and the proofreading exoribonuclease. mBio. 2018;9(2) doi: 10.1128/mBio.00221-18. e00221-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Yethindra V. Role of GS-5734 (Remdesivir) in inhibiting SARS-CoV and MERS-CoV: the expected role of GS-5734 (Remdesivir) in COVID-19 (2019-nCoV)-VYTR hypothesis. Int. J. Res. Pharm. Sci. 2020;11(SPL1):1–6. [Google Scholar]
  • 34.Cao Y.-c., Deng Q.-x., Dai S.-x. Remdesivir for severe acute respiratory syndrome coronavirus 2 causing COVID-19: an evaluation of the evidence. Trav. Med. Infect. Dis. 2020:101647. doi: 10.1016/j.tmaid.2020.101647. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Tu Y.-F., Chien C.-S., Yarmishyn A.A., Lin Y.-Y., Luo Y.-H., Lin Y.-T., Lai W.-Y., Yang D.-M., Chou S.-J., Yang Y.-P. A review of SARS-CoV-2 and the ongoing clinical trials. Int. J. Mol. Sci. 2020;21(7):2657. doi: 10.3390/ijms21072657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Yao X., Ye F., Zhang M., Cui C., Huang B., Niu P., Liu X., Zhao L., Dong E., Song C. In vitro antiviral activity and projection of optimized dosing design of hydroxychloroquine for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Li L., Li R., Wu Z., Yang X., Zhao M., Liu J., Chen D. Therapeutic strategies for critically ill patients with COVID-19. Ann. Intensive Care. 2020;10:1–9. doi: 10.1186/s13613-020-00661-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Li C., Bo L., Liu Q., Jin F. Thymosin alpha1 based immunomodulatory therapy for sepsis: a systematic review and meta-analysis. Int. J. Infect. Dis. 2015;33:90–96. doi: 10.1016/j.ijid.2014.12.032. [DOI] [PubMed] [Google Scholar]
  • 39.Bloch E.M., Shoham S., Casadevall A., Sachais B.S., Shaz B., Winters J.L., van Buskirk C., Grossman B.J., Joyner M., Henderson J.P. Deployment of convalescent plasma for the prevention and treatment of COVID-19. J Clin Invest. 2020;130(6):2757–2765. doi: 10.1172/JCI138745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Shanmugaraj B., Siriwattananon K., Wangkanont K., Phoolcharoen W. Perspectives on monoclonal antibody therapy as potential therapeutic intervention for Coronavirus disease-19 (COVID-19) Asian Pac. J. Allergy Immunol. 2020;38(1):10–18. doi: 10.12932/AP-200220-0773. [DOI] [PubMed] [Google Scholar]
  • 41.Lythgoe M.P., Middleton P. Ongoing clinical trials for the management of the COVID-19 pandemic. Trends Pharmacol. Sci. 2020;41(6):363–382. doi: 10.1016/j.tips.2020.03.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Sheikhshahrokh A., Ranjbar R., Saeidi E., Dehkordi F.S., Heiat M., Ghasemi-Dehkordi P., Goodarzi H. Frontier therapeutics and vaccine strategies for SARS-CoV-2 (COVID-19): a review. Iran. J. Public Health. 2020;49:18–29. doi: 10.18502/ijph.v49iS1.3666. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Hung I.F., To K.K., Lee C.-K., Lee K.-L., Chan K., Yan W.-W., Liu R., Watt C.-L., Chan W.-M., Lai K.-Y. Convalescent plasma treatment reduced mortality in patients with severe pandemic influenza A (H1N1) 2009 virus infection. Clin. Infect. Dis. 2011;52(4):447–456. doi: 10.1093/cid/ciq106. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Khan S., Kazmi A., Bashir N., Siddique R. COVID-19 infection: origin, transmission, and characteristics of human coronaviruses. J. Adv. Res. 2020;16:91–98. doi: 10.1016/j.jare.2020.03.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Hong-Zhi D., Xiao-Ying H., Yu-Huan M., Huang B.-S., Da-Hui L. Traditional Chinese Medicine: an effective treatment for 2019 novel coronavirus pneumonia (NCP) Chin. J. Nat. Med. 2020;18(3):206–210. doi: 10.1016/S1875-5364(20)30022-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Chen H., Guo J., Wang C., Luo F., Yu X., Zhang W., Li J., Zhao D., Xu D., Gong Q. Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: a retrospective review of medical records. Lancet. 2020;395(10226):809–815. doi: 10.1016/S0140-6736(20)30360-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Chen L., Xiong J., Bao L., Shi Y. Convalescent plasma as a potential therapy for COVID-19. Lancet Infect. Dis. 2020;20(4):398–400. doi: 10.1016/S1473-3099(20)30141-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.E.J. Giamarellos-Bourboulis, Efficiency in Management of Organ Dysfunction Associated with Infection by the Novel Sars-Cov-2 Virus (COVID-19) through A Personalized Immunotherapy Approach: the Escape Clinical TriaL.
  • 49.Chinnasamy N., Harishankar N., Kumar P.U., Rukmini C. Toxicological studies on debitterized neem oil (Azadirachta indica) Food Chem. Toxicol. 1993;31(4):297–301. doi: 10.1016/0278-6915(93)90079-e. [DOI] [PubMed] [Google Scholar]
  • 50.Greig A., Bouillant A. Binding effects of concanavalin A on a coronavirus. Can. J. Comp. Med. 1977;41(1):122. [PMC free article] [PubMed] [Google Scholar]
  • 51.Li S.-y., Chen C., Zhang H.-q., Guo H.-y., Wang H., Wang L., Zhang X., Hua S.-n., Yu J., Xiao P.-g. Identification of natural compounds with antiviral activities against SARS-associated coronavirus. Antivir. Res. 2005;67(1):18–23. doi: 10.1016/j.antiviral.2005.02.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Lau K.-M., Lee K.-M., Koon C.-M., Cheung C.S.-F., Lau C.-P., Ho H.-M., Lee M.Y.-H., Au S.W.-N., Cheng C.H.-K., Bik-San Lau C. Immunomodulatory and anti-SARS activities of Houttuynia cordata. J. Ethnopharmacol. 2008;118(1):79–85. doi: 10.1016/j.jep.2008.03.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Luo Y., Wang C.-Z., Hesse-Fong J., Lin J.-G., Yuan C.-S. Application of Chinese medicine in acute and critical medical conditions. Am. J. Chin. Med. 2019;47(6):1223–1235. doi: 10.1142/S0192415X19500629. [DOI] [PubMed] [Google Scholar]
  • 54.Chiow K., Phoon M., Putti T., Tan B.K., Chow V.T. Evaluation of antiviral activities of Houttuynia cordata Thunb. extract, quercetin, quercetrin and cinanserin on murine coronavirus and dengue virus infection. Asian Pac. J. Trop. Med. 2016;9(1):1–7. doi: 10.1016/j.apjtm.2015.12.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Ho T.-Y., Wu S.-L., Chen J.-C., Li C.-C., Hsiang C.-Y. Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction. Antivir. Res. 2007;74(2):92–101. doi: 10.1016/j.antiviral.2006.04.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Wen C.-C., Shyur L.-F., Jan J.-T., Liang P.-H., Kuo C.-J., Arulselvan P., Wu J.-B., Kuo S.-C., Yang N.-S. Traditional Chinese medicine herbal extracts of Cibotium barometz, Gentiana scabra, Dioscorea batatas, Cassia tora, and Taxillus chinensis inhibit SARS-CoV replication. Tradit. Complement. Med. 2011;1(1):41–50. doi: 10.1016/S2225-4110(16)30055-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Ulasli M., Gurses S.A., Bayraktar R., Yumrutas O., Oztuzcu S., Igci M., Igci Y.Z., Cakmak E.A., Arslan A. The effects of Nigella sativa (Ns), Anthemis hyalina (Ah) and Citrus sinensis (Cs) extracts on the replication of coronavirus and the expression of TRP genes family. Mol. Biol. Rep. 2014;41(3):1703–1711. doi: 10.1007/s11033-014-3019-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Zhang C.-H., Wang Y.-F., Liu X.-j., Lu J.-H., Qian C.-w., Wan Z.-y., Yan X.-g., Zheng H.-y., Zhang M.-Y., Xiong S. Antiviral activity of cepharanthine against severe acute respiratory syndrome coronavirus in vitro. Chin. Med. J. 2005;118(6):493. [PubMed] [Google Scholar]
  • 59.Yang C.-W., Lee Y.-Z., Kang I.-J., Barnard D.L., Jan J.-T., Lin D., Huang C.-W., Yeh T.-K., Chao Y.-S., Lee S.-J. Identification of phenanthroindolizines and phenanthroquinolizidines as novel potent anti-coronaviral agents for porcine enteropathogenic coronavirus transmissible gastroenteritis virus and human severe acute respiratory syndrome coronavirus. Antivir. Res. 2010;88(2):160–168. doi: 10.1016/j.antiviral.2010.08.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Korytkowski M., Bell D., Jacobsen C., Suwannasari R., Team F.S. A multicenter, randomized, open-label, comparative, two-period crossover trial of preference, efficacy, and safety profiles of a prefilled, disposable pen and conventional vial/syringe for insulin injection in patients with type 1 or 2 diabetes mellitus. Clin. Therapeut. 2003;25(11):2836–2848. doi: 10.1016/s0149-2918(03)80337-5. [DOI] [PubMed] [Google Scholar]
  • 61.Yang R., Liu H., Bai C., Wang Y., Zhang X., Guo R., Wu S., Wang J., Leung E., Chang H. Chemical composition and pharmacological mechanism of qingfei paidu decoction and Ma Xing Shi Gan decoction against coronavirus disease 2019 (COVID-19): in silico and experimental study. Pharmacol. Res. 2020:104820. doi: 10.1016/j.phrs.2020.104820. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Xu J., Zhang Y. Traditional Chinese medicine treatment of COVID-19, complementary therapies in clinical practice. 2020;39:101165. doi: 10.1016/j.ctcp.2020.101165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Chen Z., Nakamura T. Statistical evidence for the usefulness of Chinese medicine in the treatment of SARS. Phytother Res. 2004;18(7):592–594. doi: 10.1002/ptr.1485. An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives. [DOI] [PubMed] [Google Scholar]
  • 64.Li Y., Liu X., Guo L., Li J., Zhong D., Zhang Y., Clarke M., Jin R. Traditional Chinese herbal medicine for treating novel coronavirus (COVID-19) pneumonia: protocol for a systematic review and meta-analysis. Syst. Rev. 2020;9:1–6. doi: 10.1186/s13643-020-01343-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Yangxin S. Summary report on Lianhua Qingwen capsule/granule for the treatment of influenza. Cold Coronavirus Dis. 2019 http://en.yiling.cn/ylen/contents/2204/226.html (COVID-19), (2020) Submitted for publication. [Google Scholar]
  • 66.Fang Y.-C., Huang H.-C., Chen H.-H., Juan H.-F. TCMGeneDIT: a database for associated traditional Chinese medicine, gene and disease information using text mining. BMC Compl. Alternative Med. 2008;8(1):1–11. doi: 10.1186/1472-6882-8-58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Yang Y., Islam M.S., Wang J., Li Y., Chen X. Traditional Chinese medicine in the treatment of patients infected with 2019-new coronavirus (SARS-CoV-2): a review and perspective. Int. J. Biol. Sci. 2020;16(10):1708. doi: 10.7150/ijbs.45538. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Kim H.-Y., Shin H.-S., Park H., Kim Y.-C., Yun Y.G., Park S., Shin H.-J., Kim K. In vitro inhibition of coronavirus replications by the traditionally used medicinal herbal extracts, Cimicifuga rhizoma, Meliae cortex, Coptidis rhizoma, and Phellodendron cortex. J. Clin. Virol. 2008;41(2):122–128. doi: 10.1016/j.jcv.2007.10.011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Zhang K. Is traditional Chinese medicine useful in the treatment of COVID-19? Am. J. Emerg. Med. 2020 doi: 10.1016/j.ajem.2020.03.046. In press. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Qu D., Zheng B., Yao X., Guan Y., Yuan Z.-H., Zhong N.-S., Lu L.-W., Xie J.-P., Wen Y.-M. Intranasal immunization with inactivated SARS-CoV (SARS-associated coronavirus) induced local and serum antibodies in mice. Vaccine. 2005;23(7):924–931. doi: 10.1016/j.vaccine.2004.07.031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Wang L.-s., Wang Y.-r., Ye D.-w., Liu Q.-q. A review of the 2019 Novel Coronavirus (COVID-19) based on current evidence. Int. J. Antimicrob. Agents. 2020:105948. doi: 10.1016/j.ijantimicag.2020.105948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Gomathi M., Padmapriya S., Balachandar V. Drug studies on Rett syndrome: from bench to bedside. J. Autism Dev. Disord. 2020:1–25. doi: 10.1007/s10803-020-04381-y. [DOI] [PubMed] [Google Scholar]
  • 73.Vimalanathan S., Ignacimuthu S., Hudson J. Medicinal plants of Tamil Nadu (Southern India) are a rich source of antiviral activities. Pharmaceut. Biol. 2009;47(5):422–429. [Google Scholar]
  • 74.Tiwari B.K., Khosa R. Hepatoprotective and antioxidant effect of Sphaeranthus indicus against acetaminophen-induced hepatotoxicity in rats. J. Pharmaceut. Sci. Res. 2009;1(2):26–30. [Google Scholar]
  • 75.Keyaerts E., Vijgen L., Maes P., Neyts J., Van Ranst M. In vitro inhibition of severe acute respiratory syndrome coronavirus by chloroquine. Biochem. Biophys. Res. Commun. 2004;323(1):264–268. doi: 10.1016/j.bbrc.2004.08.085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Hussain F., Jahan N., Rahman K.-u., Sultana B., Jamil S. 2018. Identification of Hypotensive Biofunctional Compounds of Coriandrum Sativum and Evaluation of Their Angiotensin-Converting Enzyme (ACE) Inhibition Potential, Oxidative Medicine and Cellular Longevity 2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Otake T., Mori H., Morimoto M., Ueba N., Sutardjo S., Kusumoto I.T., Hattori M., Namba T. Screening of Indonesian plant extracts for anti‐human immunodeficiency virus—type 1 (HIV‐1) activity. Phytother Res. 1995;9(1):6–10. [Google Scholar]
  • 78.Yu Y.-B. The Extracts of Solanum nigrum L. for inhibitory effects on HIV-1 and its essential enzymes. Kor. J. Orient. Med. 2004;10(1):119–126. [Google Scholar]
  • 79.Ganjhu R.K., Mudgal P.P., Maity H., Dowarha D., Devadiga S., Nag S., Arunkumar G. Herbal plants and plant preparations as remedial approach for viral diseases. Virus Dis. 2015;26(4):225–236. doi: 10.1007/s13337-015-0276-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Ziai S., Heidari M. Inhibitory effects of germinal angiotensin converting enzyme by medicinal plants used in Iranian traditional medicine as antihypertensive. J. Kerman Univ. Med. Sci. 2015;16(2):134–144. [Google Scholar]
  • 81.Lee S.H., Chung N., Kwan J., Kim D.-I., Kim W.H., Kim C.J., Kim H.S., Park S.H., Seo H.S., Shin D.G. Comparison of the efficacy and tolerability of pitavastatin and atorvastatin: an 8-week, multicenter, randomized, open-label, dose-titration study in Korean patients with hypercholesterolemia. Clin. Therapeut. 2007;29(11):2365–2373. doi: 10.1016/j.clinthera.2007.11.002. [DOI] [PubMed] [Google Scholar]
  • 82.Koch S., Pong W. vol. 20. BioCentury Inc.; 2020. (First up for COVID-19: Nearly 30 Clinical Readouts before End of April). March. [Google Scholar]
  • 83.van der Hoek L., Sure K., Ihorst G., Stang A., Pyrc K., Jebbink M.F., Petersen G., Forster J., Berkhout B., Überla K. Croup is associated with the novel coronavirus NL63. PLoS Med. 2005;2(8) doi: 10.1371/journal.pmed.0020240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Gautret P., Lagier J.-C., Parola P., Meddeb L., Sevestre J., Mailhe M., Doudier B., Aubry C., Amrane S., Seng P. Clinical and microbiological effect of a combination of hydroxychloroquine and azithromycin in 80 COVID-19 patients with at least a six-day follow up: a pilot observational study. Trav. Med. Infect. Dis. 2020:101663. doi: 10.1016/j.tmaid.2020.101663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Clinical trial number NCT04317040 for "CD24Fc as a non-antiviral immunomodulator in COVID-19 treatment (SAC-COVID)" (at ClinicalTrials.gov).
  • 86.McGrath J., April All the COVID-19 vaccines and treatments currently in clinical trials. Digit. Trends. 2020 https://www.digitaltrends.com/health-fitness/coronavirus-covid-19-vaccines-treatments-list/ Retrieved 6 April 2020. [Google Scholar]
  • 87.Clinical trial number NCT04350593 for "Dapagliflozin in respiratory failure in patients with COVID-19 (DARE-19)" (at ClinicalTrials.gov).
  • 88.Koch S., Pong W. BioCentury Inc; 13 March 2020. First up for COVID-19: Nearly 30 Clinical Readouts before End of April. Retrieved 1 April 2020. [Google Scholar]
  • 89.COVID-19 Treatment Tracker (Updated 2-3x/week) Milken Institute; 2020-05-05. Retrieved 2020-05-07. [Google Scholar]
  • 90.Staines R. PharmaPhorum; 31 March 2020. Sanofi Begins Trial of Kevzara against COVID-19 Complications. Retrieved 6 April 2020. [Google Scholar]
  • 91.COVID-19 Treatment Tracker (Updated 2-3x/week) Milken Institute; 2020-05-05. Retrieved 2020-05-07. [Google Scholar]
  • 92.Clinical trial number NCT04351152 for "phase 3 study to evaluate efficacy and safety of lenzilumab in hospitalized patients with COVID-19 pneumonia" (at ClinicalTrials.gov).
  • 93.Koch S., Pong W. BioCentury Inc; 13 March 2020. First up for COVID-19: Nearly 30 Clinical Readouts before End of April. Retrieved 1 April 2020. [Google Scholar]
  • 94.Rosa S.G.V., Santos W.C. Clinical trials on drug repositioning for COVID-19 treatment. Rev. Panam. Salud Públic. 2020;44 doi: 10.26633/RPSP.2020.40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Uyeki T.M. Oxford University Press US; 2018. Oseltamivir Treatment of Influenza in Children. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Kashiouris M.G., L'Heureux M., Cable C.A., Fisher B.J., Leichtle S.W. The emerging role of vitamin C as a treatment for sepsis. Nutrients. 2020;12(2):292. doi: 10.3390/nu12020292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Wang Y., Fei D., Vanderlaan M., Song A. Biological activity of bevacizumab, a humanized anti-VEGF antibody in vitro. Angiogenesis. 2004;7(4):335–345. doi: 10.1007/s10456-004-8272-2. [DOI] [PubMed] [Google Scholar]
  • 98.Markham A., Keam S.J. Danoprevir: first global approval. Drugs. 2018;78(12):1271–1276. doi: 10.1007/s40265-018-0960-0. [DOI] [PubMed] [Google Scholar]
  • 99.Dyer O. Two Ebola treatments halve deaths in trial in DRC outbreak. BMJ Br. Med. J. (Clin. Res. Ed.) 2019;366 doi: 10.1136/bmj.l5140. [DOI] [PubMed] [Google Scholar]
  • 100.Wang Y., Xiao J., Suzek T.O., Zhang J., Wang J., Bryant S.H. PubChem: a public information system for analyzing bioactivities of small molecules. Nucleic Acids Res. 2009;37(suppl_2):W623–W633. doi: 10.1093/nar/gkp456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Zong Y., Ding M.L., Jia K.K., Ma S.T., Ju W.Z. Exploring active compounds of Da-Yuan-Yin in treatment of COVID-19 based on network pharmacology and molecular docking method. Chin. Tradit. Herb. Drugs. 2020;51(4) [Google Scholar]
  • 102.Ren J.-l., Zhang A.-H., Wang X.-J. Traditional Chinese medicine for COVID-19 treatment. Pharmacol. Res. 2020;155:104743. doi: 10.1016/j.phrs.2020.104743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Sterne J.A., Hernán M.A., Reeves B.C., Savović J., Berkman N.D., Viswanathan M., Henry D., Altman D.G., Ansari M.T., Boutron I., Robins -I. A tool for assessing risk of bias in non-randomised studies of interventions. Br. Med. J. 2016;355:i4919. doi: 10.1136/bmj.i4919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Jiang W., Shen Q., Chen M., Wang Y., Zhou Q., Zhu X., Zhu X. Levonorgestrel-releasing intrauterine system use in premenopausal women with symptomatic uterine leiomyoma: a systematic review. Steroids. 2014;86:69–78. doi: 10.1016/j.steroids.2014.05.002. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

The following is the supplementary data related to this article:Multimedia component 1
mmc1.xml (195B, xml)

Data Availability Statement

Data will be made available upon request.


Articles from Complementary Therapies in Clinical Practice are provided here courtesy of Elsevier

RESOURCES