Abstract
Background:
We aimed to use of IL-12 and IFN-γ for prevention and treatment of hydatidosis in experimental animal models.
Methods:
This experimental study was conducted in Ahvaz City, southwest of Iran in 2017. Forty female BALB/C mice with 6–8 wk old were divided into four groups (two group test and two group control). The mice were challenged with 2000 protoscolices and a combination of IL-12 (10 μg/kg) and IFN-γ (25 μg/kg) was injected intraperitoneally daily one week at the time of challenging (prevention group) and three months after challenging (treatment group). After four months, the mice were euthanized and the number, size, and weight of the cysts were measured in all studied groups. Pathologic slides were prepared from cyst wall for pathologic changes study.
Results:
There issignificant reduction in number, size, and weight of cysts in test groups.
Conclusion:
Cytokine therapy is effective methods especially for prevention of cyst formation and to treat non-operable cases. Further study of combination of chemotherapy and cytokine therapy should be investigated.
Keywords: Hydatid cyst, Cytokine therapy, Mice
Introduction
Hydatidosis is one of the important zoonotic diseases in many parts of the world. Herbivorous animals act as intermediate host to complete life cycle of parasite. Human (end host) acquired infection via ingestion of eggs which passes from feces of canine family (definitive host). Hydatid cyst is a form of larva stage of Echinococcus granulosus a cestode worm which located in small intestinal of dogs. The disease causes economic losses in animal husbandry field and costs spending in human population for surgery and other medical procedures. The distribution of the disease is worldwide especially in area with poor sanitation, poor living condition and more closer to dogs and sheep (1, 2).
Treatment of hydatid cyst in animal husbandry is not common but in human, there are many treatment approaches. Surgery is the first choice to remove the cyst in operative cases. The surgery method has some limitation for example in patients who cannot or do not want to undergo surgery, spillage of viable protoscolices and recurrence of infection with forming secondary cyst, patients with several cysts in different organs, in no operative cases due to inaccessibility of the cyst and infections after operation (3).Albendazole and other benzimidazole carbamate drugs are the second choices for treatment of inoperative cases (4).
According to immune responses to hydatid cyst, there are four type of hydatidosis by the use of ultrasonographic finding which consists type I simple cyst with no internal architecture, type II cyst with daughter cyst at periphery, type III calcified cyst, type IV complicated cyst (ruptured cyst) (5). Variety of cellular immune responses determined the outcome of the disease. The studies show the sensitive and resistant to disease, dependent on Th1 or Th2 responses. Stimulation and activity of Th1 cytokines produce IFN-γ and IL12 and lead to protection of host and destruction of the cyst whereas the activity of Th2 cytokines response induces secretion ofIL4, IL5, IL10 and IL13 which protect the parasite from protective immune reaction and cause progression of the disease (6–8).
IL12 and IFN-γ are two major cytokine of Th1 axis. IL-12 is a heterodimeric cytokine which produced by variety of immune cells like antigen presenting cells, macrophage and lymphocytes (9, 10). IL-12 promotes and stimulates Th1 activity with production of IFN-γ and other cytokines of Th1 to proliferate of lymphocytes and natural killer cell and produce macrophage aggravation (11–13).
IFN-γ is a heterodimeric cytokine and is the only member of type II class of interferons (14). The role of the IFN-γ is very important for beginning innate and adaptive immune system reactions against viral, bacterial and parasite infections. It is produced by many immune cells such as natural killer and T cells to inhibit replication of viruses and other intracellular pathogens by activation of macrophage and increasing MHC II molecule expression (15). Administration of ginger extract to infected mice can increase the IFN-γ production and therefore is effective on hydatidosis in laboratory animal model (16). Moreover, pomegranate aquatic extract has immunomodulatory effect via TNF-a regulation and has scolicidal ability in mice hydatidosis (17).
We evaluated the therapeutic effect of Th1 cytokines (IFN-γ and IL12) on hydatidosis in experimental animal model.
Materials and Methods
Animals
Forty female BALB/c mice with 6–8 wk old were obtained from Laboratory Animals Breeding Center of Ahvaz Jundishapur University of Medical Sciences in 2017. Mice were divided into four groups contained 2 group control and two groups for treatment and prophylaxis assay.
All animal right ethics principles were considered according to animal right committee protocols and the study was approved by Ethics Committee of the university.
Protoscolices preparation
Hydatid cysts were collected from infected organs of sheep in Ahvaz abattoir and transfer to parasitology laboratory of medical school. The cysts were opened under sterile condition and protoscolices were collected in sterile tubes. The protoscolices were rinsed 5 times with RPMI 1640 medium and add penicillin-streptomycin 500 unite/ml for inhibiting bacterial growth. The viability of protoscolices was tested by vital staining like eosin and more than 95% protoscolices viability were accepted for challenging BALB/c mice.
Challenging
Two thousand live protoscolices were injected intraperitoneally in BALB/c mice. In prevention group, after challenging with protoscolices, IL12 25 (10 μg/kg) (R&D systems MA USA) (18) and interferon-gamma (25 μg/kg) (R&D systems MA USA) injected intraperitoneally for 7 consecutive days (19). Serum saline was administrated in two group control (prevention and treatment). After four months the mice were euthanized by overdosage of ketamine-xylazine and the cyst were removed from peritoneal cavity and the size, number, and weight were measured in all studied group. The pathologic section was prepared from cyst wall for pathologic examination.
Statistical Analysis
Fisher exact test and chi-square were used for statistical analyzing and P.value <0.05 was considered for significant differences. The used software was SPSS (ver.21, Chicago, IL, USA)
Results
Comparison of number of Hydatid cysts in studied groups
The average number of cyst in prevention and control groups were 2 and 1551, respectively; there are significant differences between prevention and control group for number of Hydatid cyst (P<0.05). The results of treatment and control groups also showed significant differences between two groups which the number of cysts were 5.7 and 15 respectively (P<0.01). The results are presented in Table 1 and Fig. 1.
Table 1:
The number of Hydatid cyst in treatment, prevention and control groups
| Group | Number of mice | Mean | Efficacy rate (%) | Standard deviation |
|---|---|---|---|---|
| IFN γ + IL12 (Prevention) | 9 | 2.000 | 87 | 3.041 |
| IFN γ + IL12 (Treatment) | 9 | 5.7 | 63 | 3.708 |
| Control (prevention) | 8 | 15 | 0 | 4.472 |
| Control (Treatment) | 9 | 15.33 | 0 | 3.708 |
Fig. 1:
Histological Changes of Cysts in Prophylaxis (A), Treatment (B) and Control (C) Groups of Balb/c Mice
Comparison of size of Hydatid cysts in studied groups
The analysis of cysts size indicated that there are significantly differences between prevention, treatment group and control groups (P<0.001) (Table 2).
Table 2:
The size of Hydatid cyst in test and control groups of Balb/cmice
| Group | Number of mice | Mean | Efficacy rate (%) | Standard deviation |
|---|---|---|---|---|
| IFN γ + IL12 (Prevention) | 9 | 3.8 | 40 | 2.7 |
| IFN γ + IL12 (Treatment) | 9 | 4.9 | 18.3 | 3 |
| Control (prevention) | 8 | 6.3 | 0 | 2.4 |
| Control (Treatment) | 9 | 6 | 0 | 2.4 |
Comparison of weight of Hydatid cysts in studied groups
There are significant differences between prevention, treatment and control groups in weight of cysts (P<0.05) (Table 3). Fig. 2 shows the cyst in BALB/c mice in studied groups.
Table 3:
The weight of Hydatid cyst in treatment, prevention and control groups
| Group | Number of mice | Mean | Efficacy rate (%) | Standard deviation |
|---|---|---|---|---|
| IFN γ + IL12 (Prevention) | 9 | 0.13 | 93.5 | 0.29 |
| IFN γ + IL12 (Treatment) | 9 | 0.46 | 81.5 | 0.72 |
| Control (prevention) | 8 | 2 | 0 | 0.68 |
| Control (Treatment) | 9 | 2.5 | 0 | 1.18 |
Fig. 2:
The hydatid cyst in prevention (A) treatment (B) by cytokines and control (C) groups
Discussion
Using surgery and chemotherapy methods with benzimidazole family drugs is currently applied for treating human hydatidosis. Some adverse effects of two methods lead us to select the other alternative choice. The advantage of cytokine therapy is confirmed and applied for treatment or prophylaxis of some infectious diseases. The benefit of cytokine therapy in human tuberculosis was shown (20). The use of proinflammatory cytokine inhibitors may prove beneficial for tumor therapy (21). The role of Th1/Th2 in viral hepatitis (22) was evaluated. In this condition Th1/Th2 axis determined the clinical outcome (23, 24).
The benefit of cytokine therapy in visceral leishmaniasis (25, 26), asthma (27), bacterial infection (28), inflammatory diseases (29) are showed. In progressive alveolar hydatidosis cyst cases, the production and activity of Th2 cytokines such as IL-10, IL-5 and IL-2 is reported (30).
The role of Th1 cytokines in initiation of protective immune responses against pathogens agents such as viral, bacterial and parasite is well known. Two predominant Th1 cytokines are IL-12 and IFN-γ5 They stimulate and increase macrophage and NK cells population to destroy pathogen agents. The advantage of IL-12 injection to treat Leishmania major infection in BALB/c mice was presented. The treatment of infected BALB/c mice by IL-12 one week after challenging with L. major showed a significant healing due to promotion of Th1 and suppression of Th2 cytokines (31). The protective role of IL-12 has executed via induction of IFN γ production (32). The use of IL-12 in infected BALB/c mice with Trypanosoma cruzi cause a significant reduction of parasites burden by increasing IFN- γ and TNF-α levels (33). Administration of IL-12 to Schistosoma mansoni infected mice caused reduction of egg-induced pathologic changes by inhibition of granuloma formation and increasing of Th1 cytokines (34).
The present study conducted to evaluate the effect of Th1 cytokines for treating and preventing monolocular hydatid cyst in animal model. To evaluate prophylaxis effect of cytokine therapy in hydatid cyst infection, we administrated a combination of IL-12 and IFN- γ after challenging of 2000 protoscolices intraperitoneal injection. The efficacy of combination of IL-12 and IFN- γ to reduce number, weight, and size of the cyst was 87%, 93.5%, and 40% respectively when administrated at the time of challenge. The protective role of TNF-α in alveolar echinococcosis was investigated. The growth of alveolar echinococcosis was compared in two group of the BALB/c mice included LT- α TNF- α +/+ and LT- α TNF- α −/− allele. The burden of the parasites in LT- α TNF- α−/− mice were very higher than wild-type mice (LT-α TNF- α +/+ allele). The parasites load in heterozygous mice was intermediate between LT- α TNF- α −/− and wild-type mice (35). Decreasing of IFN- γ in late stage of alveolar echinococcosis infection in mice is associated with high parasite burden (36). The treatment of experimental model of alveolar echinococcosis with IFN- γ (1–5 μg twice in week for three weeks) reduced parasite burden in liver and it was suggested that administration of IFN- γ with appropriated drug is more effective (37).
The effect of IL-12 injection to E. multilocularis-infected mice (C57BL/6 J) was evaluated. The administration of IL-12 at the challenging time reduced parasite burden and inhibit development of disease. The combination of IL-12 and albendazole should be considered for treatment and prevention of alveolar echinococcosis in human (18).
We evaluated the efficacy of cytokine therapy for treatment of progressive hydatidosis condition too. A combination of IL-12 and IFN- γ administration to echinococcosis-infected mice three months after challenging, reduced number, weight and size of cyst 63%, 81.5%, and 18.3% respectively. Although the administration of cytokines after establishing infection significantly was effective, the use of cytokine therapy was more effective for prevention purpose, agreement with Emery study (18).
Conclusion
Using Th1 cytokines could be effective on treatment and prevention of hydatidosis in human especially for prevention of secondary hydatid cyst development. Further studies are needed to evaluate treatment and prevention effect of cytokine and chemotherapy combination for hydatidosis.
Acknowledgements
This article is a part of student Ph.D. thesis and financially supported by the Tropical and Infectious Diseases Researches Center of Ahvaz Jundishapur University of Medical Sciences.
Footnotes
Conflict of interest
The authors declare that there is no conflict of interests.
References
- 1.Lewall DB. Hydatid disease: Biology, pathology, imaging and classification. Clin Radiol. 1998; 53(12):863–74. [DOI] [PubMed] [Google Scholar]
- 2.Sherlock S. Hydatid disease: Disease of liver and biliary system. Oxford: Blackwell Scientific Publications; 1981. [Google Scholar]
- 3.Anadol D, Ozçelik U, Kiper N, Göçmen A. Treatment of hydatid disease. Paediatr Drugs. 2001; 3(2):123–35. [DOI] [PubMed] [Google Scholar]
- 4.Bonifacino R, Dogliani E, Craig PS. Albendazole treatment and serological follow-up in hydatid disease of bone. Int Orthop. 1997; 21(2):127–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Henry Knipe H, Gaillard F. Hydatid disease. https://radiopaedia.org/articles/hydatid-disease
- 6.Riganò R, Profumo E, Ioppolo S, Notargiacomo S, et al. Immunological markers indicating the effectiveness of pharmacological treatment in human hydatid disease. Clin Exp Immunol. 1995; 102(2):281–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Riganò R, Profumo E, Ioppolo S, Notargiacomo S, Teggi A, Siracusano A. Serum cytokine detection in the clinical follow up of patients with cystic echinococcosis. Clin Exp Immunol. 1999; 115(3):503–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Rahdar M, Rafiei A, Jamshidian M, et al. In vitro Production of IL4, IL5 and IL10 in Peripheral Blood mononuclear cell Culture from Human Hydatidosis. Biochem Cell Arch. 2005;5:29–36. [Google Scholar]
- 9.Germann T, Gately MK, Schoenhaut DS, Lohoff M, Mattner F, Fischer S, Jin SC, Schmitt E, Rüde E. Interleukin-12/T cell stimulating factor, a cytokine with multiple effects on T helper type 1 (Th1) but not on Th2 cells. Eur J Immunol. 1993; 23(8):1762–70. [DOI] [PubMed] [Google Scholar]
- 10.Kang K, Kubin M, Cooper KD, Lessin SR, Trinchieri G, Rook AH. IL-12 synthesis by human Langerhans cells. J Immunol. 1996; 156(4):1402–7. [PubMed] [Google Scholar]
- 11.D’Andrea A, Rengaraju M, Valiante NM, Chehimi J, et al. Production of natural killer cell stimulatory factor (interleukin 12) by peripheral blood mononuclear cells. J Exp Med. 1992; 176(5):1387–98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Kobayashi M, Fitz L, Ryan M, Hewick RM, et al. Identification and purification of natural killer cell stimulatory factor (NKSF), a cytokine with multiple biologic effects on human lymphocytes. J Exp Med. 1989; 170(3):827–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Wolf SF, Temple PA, Kobayashi M, et al. Cloning of cDNA for natural killer cell stimulatory factor, a heterodimeric cytokine with multiple biologic effects on T and natural killer cells. J Immunol. 1991; 146(9):3074–81. [PubMed] [Google Scholar]
- 14.Gray PW, Goeddel DV. Structure of the human immune interferon gene. Nature. 1982; 298(5877):859–63. [DOI] [PubMed] [Google Scholar]
- 15.Schoenborn JR, Wilson CB. Regulation of interferon-gamma during innate and adaptive immune responses. Adv Immunol. 2007; 96:41–101. [DOI] [PubMed] [Google Scholar]
- 16.Amri M, Touil-Boukoffa C. In vitro anti-hydatic and immunomodulatory effects of ginger and [6]-gingerol. Asian Pac J Trop Med. 2016; 9(8):749–56. [DOI] [PubMed] [Google Scholar]
- 17.Labsi M, Khelifi L, Mezioug D, Soufli I, Touil-Boukoffa C. Antihydatic and immunomodulatory effects of Punica granatum peel aqueous extract in a murine model of echinococcosis. Asian Pac J Trop Med. 2016; 9(3):211–20. [DOI] [PubMed] [Google Scholar]
- 18.Emery I, Leclerc C, Sengphommachanh K, Vuitton DA, Liance M. In vivo treatment with recombinant IL-12 protects C57BL/6 J mice against secondary alveolar echinococcosis. Parasite Immunol. 1998; 20(2):81–91. [DOI] [PubMed] [Google Scholar]
- 19.Liance M, Ricard-Blum S, Emery I, Houin R, Vuitton DA. Echinococcus multilocularis infection in mice: in vivo treatment with a low dose of ifn-γ decreases metacestode growth and liver fibrogenesis. Parasite. 1998: 5(3):231–7. [DOI] [PubMed] [Google Scholar]
- 20.Rivero-Lezcano OM. Cytokines as immunomodulators in tuberculosis therapy. Recent Pat Antiinfect Drug Discov. 2008; 3(3):168–76. [DOI] [PubMed] [Google Scholar]
- 21.Atretkhany KN, Drutskaya MS. Myeloid-Derived Suppressor Cells and Proinflammatory Cytokines as Targets for Cancer Therapy. Biochemistry (Mosc). 2016; 81(11):1274–1283. [DOI] [PubMed] [Google Scholar]
- 22.Zhang L, Hao CQ, Miao L, Dou XG. Role of Th1/Th2 cytokines in serum on the pathogenesis of chronic hepatitis C and the outcome of interferon therapy. Genet Mol Res. 2014; 13(4):9747–55. [DOI] [PubMed] [Google Scholar]
- 23.Romagnani S. The Th1/Th2 paradigm. Immunol Today. 1997; 18(6):263–6. [DOI] [PubMed] [Google Scholar]
- 24.Abbas AK, Murphy KM, Sher A. Functional diversity of helper T lymphocytes. Nature. 1996; 383(6603):787–93. [DOI] [PubMed] [Google Scholar]
- 25.Ghosh K, Sharma G, Saha A, Kar S, Das PK, Ukil A. Successful therapy of visceral leishmaniasis with curdlan involves T-helper 17 cytokines. J Infect Dis. 2013; 207(6):1016–25. [DOI] [PubMed] [Google Scholar]
- 26.de Assis Souza M, de Castro MC, de Oliveira AP, et al. Cytokines and NO in American tegumentary leishmaniasis patients: profiles in active disease, after therapy and in self-healed individuals. Microb Pathog. 2013; 57:27–32. [DOI] [PubMed] [Google Scholar]
- 27.Desai D, Brightling C. Cytokines and cytokine-specific therapy in asthma. Adv Clin Chem. 2012; 57:57–97. [DOI] [PubMed] [Google Scholar]
- 28.Khamaganova IV, Akhmedov KhB, Tarabrina NP, et al. [Effect of combined therapy using complex of natural cytokines and antimicrobial peptides in urogenital infections caused by Chlamydia and Mycoplasma]. Zh Mikrobiol Epidemiol Immunobiol. 2011;(1):90–3. [PubMed] [Google Scholar]
- 29.Mullen L, Adams G, Layward L, Vessillier S, Annenkov A, et al. Latent cytokines for targeted therapy of inflammatory disorders. Expert Opin Drug Deliv. 2014; 11(1):101–10. [DOI] [PubMed] [Google Scholar]
- 30.Kilwinski J, Jenne L, Jellen-Ritter A, et al. T lymphocyte cytokine profile at a single cell level in alveolar Echinococcosis. Cytokine. 1999;11(5):373–81. [DOI] [PubMed] [Google Scholar]
- 31.Heinzel FP, Schoenhaut DS, Rerko RM, Rosser LE, Gately MK. Recombinant interleukin 12 cures mice infected with Leishmania major. J Exp Med. 1993; 177(5):1505–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Sedegah M, Finkelman F, Hoffman SL. Interleukin 12 induction of interferon gamma-dependent protection against malaria. Proc Natl Acad Sci U S A. 1994; 91(22):10700–2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Hunter CA, Slifer T, Araujo F. Interleukin-12-mediated resistance to Trypanosoma cruzi is dependent on tumor necrosis factor alpha and gamma interferon. Infect Immun. 1996; 64(7):2381–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Wynn TA, Eltoum I, Oswald IP, Cheever AW, Sher A. Endogenous interleukin 12 (IL-12) regulates granuloma formation induced by eggs of Schistosoma mansoni and exogenous IL-12 both inhibits and prophylactically immunizes against egg pathology. J Exp Med. 1994; 179(5):1551–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Amiot F, Vuong P, Defontaines M, Pater C, Dautry F, Liance M. Secondary alveolar echinococcosis in lymphotoxin-alpha and tumour necrosis factor-alpha deficient mice: exacerbation of Echinococcus multilocularis larval growth is associated with cellular changes in the periparasitic granuloma. Parasite Immunol. 1999; 21(9):475–83. [DOI] [PubMed] [Google Scholar]
- 36.Emery I, Liance M, Deriaud E, Vuitton DA, Houin R, Leclerc C. Characterization of T-cell immune responses of Echinococcus multilocularis-infected C57BL/6J mice. Parasite Immunol. 1996; 18(9):463–72. [DOI] [PubMed] [Google Scholar]
- 37.Liance M, Ricard-Blum S, Emery I, Houin R, Vuitton DA. Echinococcus multilocularis infection in mice: in vivo treatment with a low dose of IFN-gamma decreases metacestode growth and liver fibrogenesis. Parasite. 1998; 5(3):231–7. [DOI] [PubMed] [Google Scholar]