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. 2020 Mar 25;39(5):412–417. doi: 10.1016/j.healun.2020.03.008

Epidemiologic and clinical characteristics of heart transplant recipients during the 2019 coronavirus outbreak in Wuhan, China: A descriptive survey report

Zong-Li Ren 1,1, Rui Hu 1,1, Zhi-Wei Wang 1,, Min Zhang 1, Yong-Le Ruan 1, Zhi-Yong Wu 1, Hong-Bing Wu 1, Xiao-Ping Hu 1, Zhi-Peng Hu 1, Wei Ren 1, Luo-Cheng Li 1, Fei-Feng Dai 1, Huan Liu 1, Xin Cai 1
PMCID: PMC7102567  PMID: 32362392

Abstract

BACKGROUND

The epidemiologic and clinical characteristics of heart transplant (HTx) recipients during the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) epidemic remains unclear. We studied the characteristics of HTx recipients from December 20, 2019, to February 25, 2020, in an effort to understand their risk and outcomes.

METHODS

All accessible HTx recipients were included in this single-center retrospective study. We collected information on the recipients using a web-based questionnaire as well as the hospital database.

RESULTS

We followed 87 HTx recipients (72.4% were men, and the average age was 51 years). A total of 79 recipients resided in Hubei, and 57 recipients had a Wuhan-related history of travel or contact. Most took precautionary measures while in contact with suspicious crowds, and 96.6% of the families and communities undertook prevention and quarantine procedures. Four upper airway infections were reported, and 3 of them tested negative for SARS-CoV-2 (the fourth recovered and was not tested). All cases were mild and successfully recovered after proper treatment. Laboratory results of 47 HTx cases within the last 2 months were extracted. Of these, 21.3% of recipients had pre-existing lymphopenia, and 87.2% of recipients had a therapeutic concentration of tacrolimus (5–12 ng/ml). Liver and kidney insufficiency was seen in 5 and 6 recipients, respectively.

CONCLUSION

HTx recipients who practiced appropriate prevention measures had a low rate of infection with SARS-CoV-2 and transition to the associated disease COVID-19. These early data will require confirmation as the pandemic establishes around the world.

KEYWORDS: heart transplantation, COVID-19, SARS-CoV-2, angiotensin-converting enzyme 2, immunosuppressive therapy


See Related Editorial, page 405

Since December 2019, a type of novel coronavirus (CoV) infection, later named severe acute respiratory syndrome–CoV 2 (SARS-CoV-2) by the International Committee on Taxonomy of Viruses, broke out in Wuhan, Hubei, China.1, 2, 3 The virus targets the airway epithelium using angiotensin-converting enzyme 2 (ACE2) as a receptor and causes a novel CoV-related pneumonia. Some severe cases develop into acute respiratory distress syndrome (ARDS), which can be fatal.4 The infection spread throughout China and worldwide within 2 months. As of February 25, 2020, a report from the World Health Organization indicated a total of 81,109 lab-confirmed cases from 38 countries and regions. Of those, China had more than 78,000 cases, and deaths had exceeded 2,700.5

Current epidemiologic evidence suggested that SARS-CoV-2 was highly contagious and humans were generally susceptible.6 Although most of the cases were mild or moderate and the patients recovered after proper treatment, patients with underlying morbidities carried a substantially higher mortality than those without, especially those with cardiovascular disease. Also, severe cases can develop complications other than respiratory syndromes, and reports suggest that 7% to 12% of the patients experience acute cardiac damage.2 , 7

Solid organ transplantation recipients, including heart transplant (HTx) recipients, have a higher infection risk than the normal population because of immunosuppression by anti-rejection therapy.8 , 9 However, epidemiologic and clinical characteristics of HTx recipients during the SARS-CoV-2 epidemic are largely unknown so far. We designed a comprehensive questionnaire to collect exposure history, clinical manifestations, and treatments of HTx recipients in our hospital.

Methods

All patients receiving an allograft heart transplantation and discharged between July 2015 and January 2020 in our hospital were included in this retrospective, single-center study and numbered from 1 to 87 by date of transplantation. We obtained personal information, transplantation-related history, epidemiologic history, clinical manifestations, and treatments through a web-based comprehensive questionnaire designed by clinical physicians and public health experts. The missing or unclear data collected from the questionnaire were reconciled by direct communication with the patients or their close relatives. The latest laboratory data of the recipients within the last 2 months were extracted from the hospital database. All data were finally checked and confirmed by 2 independent investigators. This study was approved by the ethics committee of Renmin Hospital of Wuhan University. Our study complies with the International Society for Heart and Lung Transplantation ethics statement.

Continuous variables were expressed as mean (standard deviation) if they were normally distributed or median (interquartile range) if they were not. Categorical variables were expressed as count and frequency. All statistical analyses were performed using SPSS software, version 26.0.

Results

Demographic data

A total of 87 recipients were included in the study and carefully followed up (Table 1 ). There were 63 men and 24 women, the average age was 51 ± 12 years, 80 (92.0%) of them lived together with relatives, and the number of relatives ranged from 1 to 8. A total of 83 (95.4%) recipients followed the pre-defined anti-rejection therapy, and there were no rejection episodes in the past 2 months, whereas 2 patients were admitted to the hospital because of bacterial infection and subsequently discharged after proper antibiotic treatment. The accompanying comorbidities in this group include hypertension (28 cases, 32.2%), hyperlipidemia (15 cases, 17.2%), diabetes (20 cases, 23.0%), new onset coronary heart disease (1 case, 1.1%), chronic obstructive pulmonary disease (1 case, 1.1%), cerebral vascular disease (6 cases, 6.9%), chronic renal dysfunction (8 cases, 12.6%), gout (6 cases, 6.9%), and hypothyroidism (1 case, 1.1%). All recipients with comorbidities were prescribed with corresponding drugs by specifically trained physicians.

Table 1.

Demographic Description of the Heart Transplant Recipients

Demographic Recipients (N = 87)
Age, years
 Mean ± SD 51 ± 12
 Range 14–73
Sex
 Male 63 (72.4%)
 Female 24 (27.6%)
Living together with relatives 80 (92.0%)
Anti-rejection therapy compliance 83 (95.4%)
Comorbidity
 Hypertension 28 (32.2%)
 Hyperlipidemia 15 (17.2%)
 Diabetes 20 (23.0%)
 New onset CHD 1 (1.1%)
 COPD 1 (1.1%)
 Cerebrovascular disease 6 (6.9%)
 Renal dysfunction 11 (12.6%)
 Gout 6 (6.9%)
 Hypothyroidism 1 (1.1%)

Abbreviations: CHD, coronary heart disease; COPD, chronic obstructive pulmonary disease.

Data are expressed as mean ± SD and n (%).

Epidemiologic and exposure history

A total of 79 recipients lived in Hubei Province, whereas 57 recipients had a Wuhan contact-related history. The whole group reported no obvious contact with patients with confirmed or suspected SARS-CoV-2–associated disease COVID-19. Protective procedures were initiated with 11 of 16 recipients (68.8%) who were in contact with asymptomatic individuals who traveled to or came back from Wuhan. After January 23, 2020, 84 of 87 recipients (96.6%) undertook precautionary procedures in their community. Of these 87 recipients, 56 (64.4%) self-quarantined at home by more than 1 week. The other major exposure history is presented in Table 2 .

Table 2.

Exposure History of the Recipients

Exposure history Recipients (N = 87)
Have been to Wuhan 57 (65.5%)
Contact with 2019-nCoV patients 0 (0.0%)
Contact with asymptomatic individual with epidemic history 16 (18.4%)
 Precautionary procedure 11/16 (68.8%)
Take public transport 25 (28.7%)
 Precautionary procedure 24/25 (96.0%)
Have been to crowded place 19 (21.8%)
 Precautionary procedure 18/19 (94.7%)
Attend group events 5 (5.7%)
 Precautionary procedure 3/5 (60.0%)
Animal or poultry touch 16 (18.4%)
 Animal death 0/16 (0.0%)
Precautionary procedure in the family 84 (96.6%)
 Mask 71/84 (84.5%)
 Hand wash 75/84 (89.3%)
 Sanitization 52/84 (61.9%)
Precautionary procedure in the community 84 (96.6%)
 Daily body temperature and symptoms monitoring 63/84 (75.0%)
 Unified living supplies purchasing and distribution 59/84 (70.2%)
 Community shutting down and no passing 72/84 (85.7%)
Self-quarantine at home 56 (64.4%)
 22–28 days 52/56 (92.9%)
 15–21 days 3/56 (5.4%)
 8–14 days 1/56 (1.8%)

Abbreviation: nCoV, novel coronavirus.

Data are expressed as n (%) and n/N (%).

Laboratory results

Laboratory results of 47 recipients within the last 2 months were identified and extracted from the database, including blood routine, tacrolimus concentration, and liver and kidney function examination (Table 3 ). The average white blood cell count was 7.2 ± 2.2 × 109 cells/liter, and 6 (6 of 47, 12.8%) recipients had an abnormal white blood cell count, including 5 that were elevated. The average neutrophil percentage was 60.4% ± 12.1%, 5 recipients were abnormal. The average lymphocyte percentage was 27.7% ± 9.9%, although 10 (10 of 47, 21.3%) recipients had lymphopenia and 31 (31 of 47, 66.0%) recipients had a lymphocyte percentage lower than 30%. The average tacrolimus concentration was 7.6 ± 2.4 ng/ml, which was therapeutic. Examination of liver and renal function was evaluated by alanine aminotransferase, aspartate aminotransferase, urea, and creatinine assessments, and the average results were grossly normal, although 5 and 6 recipients had liver or kidney insufficiency, respectively.

Table 3.

Laboratory Results of the Recipients

Lab result Recipients (N = 47)
Blood routine
 WBC count (× 109 cells/liter) 7.2 ± 2.2
 Abnormal WBC count 6 (12.8%)
 Neu% 60.4 ± 12.1
 Abnormal Neu% 5 (10.6%)
 Lym% 27.7 ± 9.9
 <20% 10 (21.3%)
 20%–30% 21 (44.7%)
 30%–40% 10 (21.3%)
 40%–50% 5 (10.6%)
 >50% 1 (2.1%)
FK506, ng/ml 7.6 ± 2.4
 <5.0 4 (8.5%)
 5.0–7.9 25 (53.2%)
 8.0–11.9 16 (34.0%)
 ≥12.0 2 (4.3%)
Biochemistry
 ALT, U/liter 22.6 ± 17.8
 AST, U/liter 25.5 ± 18.7
 Abnormal ALT or AST 5 (10.6%)
 Urea, mmol/liter 8.6 ± 3.0
 Cr, µmol/liter 92.9 ± 38.4
 Abnormal Urea or Cr 6 (12.8%)

Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase; Cr, creatinine; Lym%, lymphocyte percentage; Neu%, neutrophilic granulocyte percentage; WBC, white blood cell.

Data are mean ± SD and n (%).

Clinical characteristics of recipients with airway infection

There were 4 upper airway infections reported during this time period (Table 4 ). Three of them were tested for SARS-CoV-2 infection and were negative. The other recipient with an upper airway infection recovered after 6 days and was not tested for SARS-CoV-2 because the specific test kit had not yet launched during the early stage of the SARS-CoV-2 epidemic. All of them were tested for influenza A and B, and 1 upper airway infection recipient was confirmed with influenza A infection. All 4 recipients successfully recovered after proper therapies.

Table 4.

Clinical Characteristics of the Recipients with Airway Infection

Patient number Date of onset Symptom Blood routine Test for airway pathogen Chest CT report Diagnosis Treatment Outcome
17 December 31, 2019 Nasal obstruction WBC 11.34 × 109, Neu% 71.6%, Lym% 18.7% SARS-Cov-2 (N/A), FluA (−), FluB (−) Negative Upper airway infection Antibiotics Recovered
44 January 28, 2020 Fever, nasal obstruction WBC 6.36 × 109, Neu% 76.4%, Lym% 13.9% SARS-Cov-2 (−), FluA (+), FluB(−) Negative Upper airway infection; FluA Antibiotics, anti-viral drugs Recovered
58 February 2, `2020 Dry cough WBC 5.3 × 109, Neu% 89.5%, Lym% 5.7% SARS-Cov-2 (−), FluA (−), FluB (−), HPIV (−), RSV (−), Adv (−), Mpn (−), Cpn(−) Viral pneumonia Lower airway infection,
viral pneumonia
Antibiotics, anti-viral drugs Recovered
70 January 19, 2020 Fever WBC 4.3 × 109, Neu% 74.7%, Lym% 12.3% SARS-Cov-2 (−), FluA (−), FluB (−), HPIV (−), RSV (−), Adv (−), Mpn (−), Cpn(−) Pulmonary infection Lower airway infection,
pulmonary infection
Antibiotics Recovered

Abbreviations: (+), positive; (−), negative; Adv, adenovirus; Cpn, chlamydia pneumoniae; CT, computed tomography; FluA, influenza A; FluB, influenza B; HPIV, parainfluenza virus; Lym%, lymphocyte percentage; Mpn, mycoplasma pneumoniae; N/A, not applied; Neu%, neutrophilic granulocyte percentage; RSV, respiratory syncytial virus; SARS-Cov-2, severe acute respiratory syndrome coronavirus 2; WBC, white blood cell.

Discussion

This is the largest comprehensive report of HTx recipients during the SARS-CoV-2 epidemic, and our findings indicated that this immunocompromised population received similar exposure, including contact with individuals with travel from Wuhan, taking public transport, and going to crowded places; however, they exhibited less infection than expected.

The origins of this virus have been traced back to the seafood wholesale market in Wuhan, China.4 In our epidemiologic investigation, 16 recipients experienced contact with animals or poultry, but there was no reported animal death. No recipients have ever been to the seafood wholesale market in Wuhan or were in contact with any potential supply chains of wild or game meat.

SARS-CoV-2 mainly spreads through the respiratory tract, and survival time of SARS-CoV-2 in air may be somewhat limited. Any protective measures that block the transmission pathway can reduce the risk of infection. According to our investigation of epidemiologic history, it would be reasonable to infer that although HTx recipients have a similar epidemiologic history to the normal population, they may have a better protection awareness and use of precautions as a usual practice during the SARS-CoV-2 epidemic.

Studies have shown that people are generally susceptible to CoV. CoVs such as SARS-CoV and Middle East respiratory syndrome (MERS)-CoV also caused severe lower respiratory tract infection with ARDS, extrapulmonary manifestations, and multiorgan dysfunction syndrome among both immunocompetent and immunocompromised hosts, with mortality rates of 10% and 35%, respectively.10 , 11 Early patient reports from SARS-CoV-2 find similar trends. Severe manifestations, even death, with SARS-CoV-2 have been associated in elderly patients with comorbidities, including hypertension, diabetes, and heart and/or kidney disease.3 This finding is similar to increased severity and death in elderly patients following both SARS and MERS-CoV infection.12 , 13 For the MERS-CoV outbreak, smoking, hypertension, diabetes, cardiovascular disease, and/or other chronic illnesses were present in most deaths and correspond to findings in animal models.14 The accompanying comorbidities in this group of HTx recipients include hypertension (28 cases, 34.2%), hyperlipidemia (15 cases, 17.2%), diabetes (20 cases, 23.0%), new onset coronary heart disease (1 case, 1.1%), chronic obstructive pulmonary disease (1 case, 1.1%), cerebrovascular disease (6 cases, 6.9%), chronic renal dysfunction (11 cases, 12.6%), hyperuricemia (6 cases, 6.9%), and hypothyroidism (1 case, 1.1%), and the average age is 50.5 ± 11.7 years. Thus, it would indicate that vigilance is necessary for these immunocompromised recipients following SARS-CoV-2 infection.

Our results are unexpected because only 4 recipients got airway infection and 3 of them had a negative SARS-CoV-2 result. This is similar to the information from the Organ Transplant Center in our hospital, where only 2 cases were reported with SARS-CoV-2 infection in renal transplantation.15 Data from Ju et al.16 suggest that the number of solid organ transplantation recipients in China suffering from SARS-CoV-2 infection are few, including only 9 confirmed cases altogether. With limited data, it is difficult to determine the populations that may be most susceptible to SARS-CoV-2. More data are needed to determine the susceptibility of the immunocompromised population.

CoVs are positive-strand RNA viruses, which primarily target mucosal surfaces of respiratory and intestinal tracts to establish an infection.17 , 18 Epithelial cell surface components are exploited as primary receptors to mediate viral entry and the establishment of a viral infection.19 One integral protease of the renin-angiotensin system (RAS), ACE2, which is a major physiologic regulator of the cardiovascular system, facilitates cellular entry of human CoVs.20 , 21 Recently, ACE2 had been identified as a receptor for SARS-CoV-2.22 , 23 ACE2 is thought to be a key regulator in maintenance of RAS homeostasis.24 , 25 Several studies illustrate the possible mechanism of immunosuppressants in activating RAS.26, 27, 28, 29, 30 Ferrario et al.31 demonstrated that the treatment of cultured astrocytes with angiotensin-II caused a marked reduction in neural ACE2 mRNA and protein, mediated with either losartan or both losartan and lisinopril by the AT1 receptor. It is unclear what, if any, difference in the expression of pulmonary ACE2 exists in the presence of immunosuppression, and investigating the difference in ACE2 between the recipients and the normal population would provide further evidence.

Similar to SARS-CoV and MERS-CoV infection, patients with SARS-CoV-2 infections exhibit symptoms of viral pneumonia, including fever, cough, or dyspnea, and bilateral lung infiltration in severe cases. All these 3 CoVs induce excessive and aberrant non-effective host immune responses that are associated with severe lung pathology, leading to death.32 The autopsy results of deceased patients indicate diffuse alveolar damage with alveolar edema, focal hemorrhage, and hyaline membrane formation,33 which are similar to the pathologic manifestations of ARDS.34 However, most SARS-CoV-2 infections were mild or moderate cases; meanwhile, case reports showed that the clinical manifestations and progression of SARS-CoV-2 infection in renal transplant recipients were generally consistent with common SARS-CoV-2 infected patients.15 According to our investigation of epidemiologic history, we could not deny the possibility of contacting and getting infected with SARS-CoV-2 in HTx recipients. It is important to note that laboratory data may be misleading in HTx recipients because several of our patients already exhibited lymphopenia, which may be a result of the use of immunosuppressants that prevent lymphocyte development and proinflammatory cytokines gene expression, such as IL-2, IL-3, IL-4, interferon-γ, and tumor necrosis factor-α.35, 36, 37, 38 Glucocorticoids inhibit immune responses by negatively regulating immunocytes39, 40, 41, 42, 43, 44 and especially weaken the strength of the T-cell receptor signal, which is important in T-cell activation and differentiation.45 Thus, we imply that if HTx recipients are infected with SARS-CoV-2, they may not exhibit typical manifestations in the early stage because of the presence of immunosuppression. Our data suggest that maintaining the blood trough concentration of FK506 at 7.9 ± 2.9 ng/ml is appropriate. However, the appropriate degree of immunosuppression needs further verification.

There are several limitations in this study. First, the detailed clinical data for the recipients with airway symptoms were not fully extracted because of the variation of the database in different hospitals. Second, it is reported that SARS-CoV-2 may have an extremely long incubation time, so longer observation and follow up are warranted. Furthermore, a larger sample size will contribute to greater reliability of the data. Furthermore, recall bias, which would be hard to avoid in a survey-based investigation, should also be noted as a limitation.

In conclusion, according to our investigation, we suggest that HTx recipients who used enhanced protection measures during the SARS-CoV-2 outbreak did not have a substantially higher rate of infection among the population. It is also important to note that immunosuppressed patients may not exhibit typical manifestations and might present confusing laboratory data, thus obfuscating diagnosis in some cases. These early data will require confirmation as the pandemic establishes around the world.

Disclosure statement

The authors have no conflict of interest to disclose. The authors acknowledge all health workers involved in the diagnosis and treatment of patients in China. The authors thank the World Health Organization for sharing data collection templates publicly on the website. This study was supported by grants from National Natural Science Foundation of China (81501376) and Postdoctoral Research Foundation of China (2017M620339). This study was approved by the ethical review committee of Renmin Hospital of Wuhan University.

The article published from China may include patients transplanted at a time when concerns existed with unethical procurement of organ donors and therefore may represent a violation of the publication policy. However, the editors have chosen to override this aspect because of the critical importance of the information provided in such a paper for the benefit and help of our patients while recognizing the dignity of those from whom the unethical organs were most probably obtained.

References

  • 1.Zhu N, Zhang D, Wang W. A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med. 2020;382:727–733. doi: 10.1056/NEJMoa2001017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Huang C, Wang Y, Li X. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395:497–506. doi: 10.1016/S0140-6736(20)30183-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Chen N, Zhou M, Dong X. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395:507–513. doi: 10.1016/S0140-6736(20)30211-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Zhou P, Yang XL, Wang XG. A pneumonia outbreak associatedwith a new coronavirus of probable bat origin. Nature. 2020;579:270–273. doi: 10.1038/s41586-020-2012-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.WHO>World Health Organization. Available at: https://www.who.int.
  • 6.5th ed. 2020. New coronavirus pneumonia prevention and control program in China. [in Chinese] [Google Scholar]
  • 7.Wang D, Hu B, Hu C, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China [e-pub ahead of print]. JAMA. doi: 10.1001/jama.2020.1585, Accessed February 25, 2020. [DOI] [PMC free article] [PubMed]
  • 8.Shi B. Current development of the organ transplantation in China, past and future. Organ Transpl. 2019;10:32–35. [in Chinese] [Google Scholar]
  • 9.Huang J. Induction and maintenance of immunosuppression in heart transplantation. Chin Transpl J. 2018;12:49–54. [in Chinese] [Google Scholar]
  • 10.Peiris JS, Lai ST, Poon LL. Coronavirus as a possible cause of severe acute respiratory syndrome. Lancet. 2003;361:1319–1325. doi: 10.1016/S0140-6736(03)13077-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Yeung ML, Yao Y, Jia L. MERS coronavirus induces apoptosis in kidney and lung by upregulating Smad7 and FGF2. Nat Microbiol. 2016;1:16004. doi: 10.1038/nmicrobiol.2016.4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Hung IF, Cheng VC, Wu AK. Viral loads in clinical specimens and SARS manifestations. Emerg Infect Dis. 2004;10:1550–1557. doi: 10.3201/eid1009.040058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Assiri A, Al-Tawfiq JA, Al-Rabeeah AA. Epidemiological, demographic, and clinical characteristics of 47 cases of Middle East respiratory syndrome coronavirus disease from Saudi Arabia: a descriptive study. Lancet Infect Dis. 2013;13:752–761. doi: 10.1016/S1473-3099(13)70204-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Rahman A, Sarkar A. Risk factors for fatal Middle East respiratory syndrome coronavirus infections in Saudi Arabia: analysis of the WHO line list, 2013-2018. Am J Public Health. 2019;109:1288–1293. doi: 10.2105/AJPH.2019.305186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Tu Y, Wu X, Liu F. A clinical report of 2 cases of renal transplant recipients with newly developed coronavirus pneumonia. Chin J Organ Transplant. 2020;41:E005. [in Chinese] [Google Scholar]
  • 16.Ju C, Li L, Qiu T, Xue W, Shi B. Clinical characteristics of novel coronavirus pneumonia in transplant recipients and management strategies during the outbreak. Anti-new coronary pneumonia column. 1st ed [in Chinese]. Available at:http://www.cotdf.org/index.php?m=content&c=index&a=show&catid=19&id=1144.
  • 17.González JM, Gomez-Puertas P, Cavanagh D, Gorbalenya AE, Enjuanes L. A comparative sequence analysis to revise the current taxonomy of the family Coronaviridae. Arch Virol. 2003;148:2207–2235. doi: 10.1007/s00705-003-0162-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Weiss SR, Navas-Martin S. Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus. Microbiol Mol Biol Rev. 2005;69:635–664. doi: 10.1128/MMBR.69.4.635-664.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Wevers BA, Hoek Lvd. Renin–angiotensin system in human coronavirus pathogenesis. Future Virol. 2010;5:145–161. doi: 10.2217/fvl.10.4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Kuba K, Imai Y, Rao S. A crucial role of angiotensin converting enzyme 2 (ACE2) in SARS coronavirus–induced lung injury. Nat Med. 2005;11:875–879. doi: 10.1038/nm1267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Li W, Moore MJ, Vasilieva N. Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426:450–454. doi: 10.1038/nature02145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Xu X, Chen P, Wang J. Evolution of the novel coronavirus from the ongoing Wuhan outbreak and modeling of its spike protein for risk of human transmission. Sci China. Life Sci. 2020;63:457–460. doi: 10.1007/s11427-020-1637-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Xu H, Zhong L, Deng J. High expression of ACE2 receptor of 2019-nCoV on the epithelial cells of oral mucosa. Int J Oral Sci. 2020;12:8. doi: 10.1038/s41368-020-0074-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Kurdi M, De Mello WC, Booz GW. Working outside the system: an update on the unconventional behavior of the renin-angiotensin system components. Int J Biochem Cell Biol. 2005;37:1357–1367. doi: 10.1016/j.biocel.2005.01.012. [DOI] [PubMed] [Google Scholar]
  • 25.Gallagher PE, Chappell MC, Ferrario CM, Tallant EA. Distinct roles for ANG II and ANG-(1-7) in the regulation of angiotensin-converting enzyme 2 in rat astrocytes. Am J Physiol Cell Physiol. 2006;290:C420–C426. doi: 10.1152/ajpcell.00409.2004. [DOI] [PubMed] [Google Scholar]
  • 26.Letizia C, D'Ambrosio C, De Ciocchis A, Scavo D, Pozzilli P. Serum angiotensin-converting enzyme levels in patients with recent-onset insulin-dependent diabetes after one year of low-dose cyclosporin therapy. IMDIAB study group. Int J Clin Pharmacol Res. 1995;15:209–213. [PubMed] [Google Scholar]
  • 27.Hošková L, Málek I, Kautzner J. Tacrolimus-induced hypertension and nephrotoxicity in Fawn-Hooded rats are attenuated by dual inhibition of renin-angiotensin system. Hypertens Res. 2014;37:724–732. doi: 10.1038/hr.2014.79. [DOI] [PubMed] [Google Scholar]
  • 28.Kupferman JC, Beaudoin R, Carr R. Activation of the renal renin-angiotensin system by cyclosporine A and FK 506 in the rat. Transplant Proc. 1994;26:2891–2893. [PubMed] [Google Scholar]
  • 29.Julien J, Farge D, Kreft-Jais C. Cyclosporine-induced stimulation of the renin-angiotensin system after liver and heart transplantation. Transplantation. 1993;56:885–891. doi: 10.1097/00007890-199310000-00022. [DOI] [PubMed] [Google Scholar]
  • 30.Schreiber SL, Crabtree GR. The mechanism of action of cyclosporin A and FK506. Immunol Today. 1992;13:136–142. doi: 10.1016/0167-5699(92)90111-J. [DOI] [PubMed] [Google Scholar]
  • 31.Ferrario CM, Jessup J, Chappell MC. Effect of angiotensin-converting enzyme inhibition and angiotensin II receptor blockers on cardiac angiotensin-converting enzyme 2. Circulation. 2005;111:2605–2610. doi: 10.1161/CIRCULATIONAHA.104.510461. [DOI] [PubMed] [Google Scholar]
  • 32.Zumla A, Hui DS, Azhar EI, Memish ZA, Maeurer M. Reducing mortality from 2019-nCoV: host-directed therapies should be an option. Lancet. 2020;395:e35–e36. doi: 10.1016/S0140-6736(20)30305-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Xu Z, Shi L, Wang Y. Pathological findings of COVID-19 associated with acute respiratory distress syndrome [e-pub ahead of print] Lancet Respir Med. 2020 doi: 10.1016/S2213-2600(20)30076-X. Accessed February 25, 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Nicholls JM, Poon LL, Lee KC. Lung pathology of fatal severe acute respiratory syndrome. Lancet. 2003;361:1773–1778. doi: 10.1016/S0140-6736(03)13413-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Liu J, Farmer JD, Jr, Lane WS, Friedman J, Weissman I, Schreiber SL. Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes. Cell. 1991;66:807–815. doi: 10.1016/0092-8674(91)90124-h. [DOI] [PubMed] [Google Scholar]
  • 36.Liu J, Albers MW, Wandless TJ. Inhibition of T cell signaling by immunophilin-ligand complexes correlates with loss of calcineurin phosphatase activity. Biochemistry. 1992;31:3896–3901. doi: 10.1021/bi00131a002. [DOI] [PubMed] [Google Scholar]
  • 37.Eugui EM, Almquist SJ, Muller CD, Allison AC. Lymphocyte-selective cytostatic and immunosuppressive effects of mycophenolic acid in vitro: role of deoxyguanosine nucleotide depletion. Scand J Immunol. 1991;33:161–173. doi: 10.1111/j.1365-3083.1991.tb03746.x. [DOI] [PubMed] [Google Scholar]
  • 38.Blaheta RA, Leckel K, Wittig B. Mycophenolate mofetil impairs transendothelial migration of allogeneic CD4 and CD8 T-cells. Transplant Proc. 1999;31:1250–1252. doi: 10.1016/s0041-1345(98)01984-8. [DOI] [PubMed] [Google Scholar]
  • 39.Takahira R, Yonemura K, Fujise Y, Hishida A. Dexamethasone attenuates neutrophil infiltration in the rat kidney in ischemia/reperfusion injury: the possible role of nitroxyl. Free Radic Biol Med. 2001;31:809–815. doi: 10.1016/s0891-5849(01)00658-x. [DOI] [PubMed] [Google Scholar]
  • 40.Abe M, Thomson AW. Dexamethasone preferentially suppresses plasmacytoid dendritic cell differentiation and enhances their apoptotic death. Clin Immunol. 2006;118:300–306. doi: 10.1016/j.clim.2005.09.019. [DOI] [PubMed] [Google Scholar]
  • 41.Ehrchen J, Steinmüller L, Barczyk K. Glucocorticoids induce differentiation of a specifically activated, anti-inflammatory subtype of human monocytes. Blood. 2007;109:1265–1274. doi: 10.1182/blood-2006-02-001115. [DOI] [PubMed] [Google Scholar]
  • 42.Suda T, Chida K, Matsuda H. High-dose intravenous glucocorticoid therapy abrogates circulating dendritic cells. J Allergy Clin Immunol. 2003;112:1237–1239. doi: 10.1016/j.jaci.2003.09.028. [DOI] [PubMed] [Google Scholar]
  • 43.Cupic B, Breljak D, Gabrilovac J. Receptor-mediated down-regulation of neutral endopeptidase (NEP; EC 3.4.24.11; CD10) on immature B lymphocytes by dexamethasone. Int J Mol Med. 2005;15:1023–1031. [PubMed] [Google Scholar]
  • 44.Youinou P, Pers JO. The late news on BAFF in autoimmune diseases. Autoimmun Rev. 2010;9:804–806. doi: 10.1016/j.autrev.2010.06.011. [DOI] [PubMed] [Google Scholar]
  • 45.Harr MW, Rong Y, Bootman MD, Roderick HL, Distelhorst CW. Glucocorticoid-mediated inhibition of Lck modulates the pattern of T cell receptor-induced calcium signals by down-regulating inositol 1,4,5-trisphosphate receptors. J Biol Chem. 2009;284:31860–31871. doi: 10.1074/jbc.M109.005579. [DOI] [PMC free article] [PubMed] [Google Scholar]

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