Interaction of hepatitis C virus with the immune system in pregnant women with chronic hepatitis C
https://doi.org/10.17749/2313-7347.2019.13.1.043-049
Abstract
Aim: to analyze the relation between hepatitis C virus (HCV) load, the immune reactivity, and the immune-mediated lesions in the liver during pregnancy in women with chronic hepatitis C (CHC). Materials and methods. The study included 1690 pregnant women, 107 of whom had IgG antibodies to HCV; in addition, 68 women (63.5 %) were diagnosed with chronic hepatitis C and had a positive test for HCV RNA. The diagnosis of CHC was confirmed by determining serum total anti-HCV IgG antibodies using an enzyme immunoassay. The qualitative and quantitative determination of HCV RNA in the blood was performed by polymerase chain reaction. The virus replicative activity was qualitatively assessed by the viral load: low - the level of HCV RNA was up to 103 lU/ml, moderate - from 103 to 106 lU/ml, and high - above 106 lU/ml. To quantify the results, we used the positivity index, i.e, the ratio of the serum optical density to the critical optical density (cut-off) in each test. Results. In the early stages of pregnancy, signs of severe immune-mediated hepatocyte injury persisted. In the II and Ill trimesters, there was an unusual discrepancy between the severity of viral load and the degree of hepatocyte injury as the course of CHC remained usual. Another evidence of the liver involvement in this immune-pathological mechanism was an 87 % decrease in alanine aminotransferase activity with an increase in the viral load in patients with CHC in the Ill trimester of pregnancy. Conclusion. Suppression of anti-HCV humoral immunity, but not cellular immunity, begins from early stages of pregnancy and is accompanied by a significant increase in hepatocyte lesions without an increase in the severity of the inflammatory process.
About the Authors
A. P. TsibulkinRussian Federation
Anatoliy P. Tsibulkin - MD, PhD, Professor, Head of Department of Clinical Laboratory Diagnostics, KSMA - branch of RMACPE HM of RF.
36 Butlerova Str., Kazan 420012.
Tel:. +7(843)2333472.
I. M. Khaertynova
Russian Federation
Ilsiyar M. Khaertynova - MD, PhD, Professor, Head of the Department of Infectious Diseases, KSMA - branch of RMACPE HM of RF.
36 Butlerova Str., Kazan 420012.
Tel:. +7(843)2678117.
G. F. Leonova
Russian Federation
Gulnara F. Leonova - Assistant, Department of Infectious Diseases, KSMA - branch of RMACPE HM of RF.
36 Butlerova Str., Kazan 420012.
Tel:. +7(843)2678117.
L. I. Maltseva
Russian Federation
Larisa I. Maltseva - MD, PhD, Professor, Department of Obstetrics and Gynecology, KSMA - branch of RMACPE HM of RF.
36 Butlerova Str., Kazan 420012.
Tel.: +7(905)3144051.
References
1. Sorinson S.N. Viral hepatitis. [Virusnye gepatity]. 2-e izd. SPb.: Teza, 1998. 336 s. (In Russ.).
2. Rehermann B. Hepatitis C virus versus innate and adaptive immune responses: a tale of coevolution and coexistence. J Clin Invest. 2009;119(7):1745-54. DOI: 10.1172/JCI39133.
3. Ivashkin V.T. The immune system and liver damage in chronic hepatitis B and C. [Immunnaya sistema i povrezhdeniya pecheni pri hronicheskih gepatitah V i S]. Rossijskij zhurnal gastroehnterologii, gepatologii, koloproktologii. 2009;19(6):4-10. (In Russ.).
4. Chang K.M. Immune pathogenesis of viral hepatitis B and C. In: Zakim and Boyer's hepatology: a textbook of liver disease. Eds. D. Boyer, M.P. Manns, A.J. Sanyal. 6th ed. Saunders, 2012. 111-28.
5. Fahey L.M., Brooks D.G. Opposing positive and negative regulation of T cell activity during viral persistence. Curr Opin Immunol. 2010;22(3):348-54. DOI: 10.1016/j.coi.2010.03.004.
6. Napoli J., Bishop G.A., McGuinness P.H. et al. Progressive liver injury in chronic hepatitis C infection correlates with increased intrahepatic expression of Th1-associated cytokines. Hepatology. 1996;24(4):759-65. DOI: 10.1002/hep.510240402.
7. Lechner F., Wong D.K., Dunbar P.R. et al. Analysis of successful immune responses in persons infected with hepatitis C virus. J Exp Med. 2000;191(9):1499-512. DOI: 10.1084/jem.191.9.1499.
8. Kaplan D.E. Immunopathogenesis of hepatitis C virus infection. Gastroenterol Clin North Am. 2015; 44(4):735-60. DOI: 10.1016/j.gtc.2015.07.004.
9. Latt N.C., Spencer J.D., Beeby P.J. et al. Hepatitis C in injecting drug-using women during and after pregnancy. J Gastroenterol Hepatol. 2000;15(2):175-81. DOI: 10.1046/j.1440-1746.2000.02060.x.
10. Veenstra van Nieuwenhoven A.L., Heineman M.J., Faas M.M. The immunology of successful pregnancy. Hum Reprod Update. 2003;9(4):347-57. DOI: 10.1093/humupd/dmg026.
11. Conte D., Fraquelli M., Prati D. et al. Prevalence and clinical course of chronic hepatitis C virus (HCV) infection and rate of HCV vertical transmission in a cohort of 15,250 pregnant women. Hepatology. 2000;31(3):751-5. DOI: 10.1002/hep.510310328.
12. Mor G., Cardenas I. The immune system in pregnancy: a unique complexity. Am J Reprod Immunol. 2010;63(6):425-33. DOI: 10.1111/j.1600-0897.2010.00836.x.
13. Munoz-Suano A., Hamilton A.B., Betz A.G. Gimme shelter: the immune system during pregnancy. Immunol Rev. 2011;241(1):20-38. DOI: 10.1111/j.1600-065X.2011.01002.x.
14. Somerset D.A., Zheng Y., Kilby M.D. et al. Normal human pregnancy is associated with an elevation in the immune suppressive CD25+ CD4+ regulatory T-cell subset. Immunology. 2004;112(1):38-43. DOI: 10.1111/j.1365-2567.2004.01869.x.
15. Mor G., Cardenas I., Abrahams V. et al. Inflammation and pregnancy: the role of the immune system at the implantation site. Ann N Y Acad Sci. 2011;1221:80-7. DOI: 10.1111/j.1749-6632.2010.05938.x.
16. Zenclussen A.C. Regulatory T cells in pregnancy. Springer Semin Immun. 2006;28(1):31-9. DOI: 10.1007/s00281-006-0023-6.
17. Guerin L.R., Prins J.R., Robertson S.A. Regulatory T-cells and immune tolerance in pregnancy: a new target for infertility treatment? Hum Reprod Update. 2009;15(5):517-35. DOI: 10.1093/humupd/dmp004.
18. Sofronova N.N., Tsibulkin A.P., Khaertynova I.M. et al. Specific circulating immune complexes in patients with chronic HCV-infection. [Specificheskie cirkuliruyushchie immunnye kompleksy u bol'nyh hronicheskoj HCV-infekciej]. Prakticheskaya medicina. 2015;7(92):100-5. (In Russ.).
19. Ivashkin V.T. Mechanisms of immune tolerance and liver disease. [Mekhanizmy immunnoj tolerantnosti i patologii pecheni]. Rossijskij zhurnal gastroehnterologii, gepatologii, koloproktologii. 2008;19(2):8-13. (In Russ.).
20. Sappenfield E., Jamieson D.J., Kourtis A.P. Pregnancy and susceptibility to infectious diseases. Infect Dis Obstet Gynecol. 2013;2013:752852. DOI: 10.1155/2013/752852.
21. Leonova G.F. Clinical and epidemiological characteristics of chronic hepatitis C in children. [Kliniko-epidemiologicheskaya harakteristika hronicheskogo gepatita S u detej]. Avtoref. dis. kand. med. nauk. Kazan1, 2014. 19 s. (In Russ.).
Review
For citations:
Tsibulkin A.P., Khaertynova I.M., Leonova G.F., Maltseva L.I. Interaction of hepatitis C virus with the immune system in pregnant women with chronic hepatitis C. Obstetrics, Gynecology and Reproduction. 2019;13(1):43-49. (In Russ.) https://doi.org/10.17749/2313-7347.2019.13.1.043-049

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