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Induction of IgA and sustained deficiency of cell proliferative response in chronic hepatitis C
Yalena Amador-Cañizares1, Liz Alvarez-Lajonchere, Ivis Guerra
1HCV Department, Vaccine Division, Centro de Ingeniería Genética y Biotecnología, Ave 31, 58 and 190, Playa, P.O. Box 6162, Havana, Cuba. yalena.amador@cigb.edu.cu
Insights
Chronic hepatitis C virus (HCV) infection shows a strong antibody response but a weak cellular immune response. IgA levels correlate with liver damage, suggesting potential diagnostic value.
Area of Science:
- Immunology
- Virology
- Hepatology
Background:
- Hepatitis C virus (HCV) infection can lead to chronic liver disease.
- Understanding the immune response in chronic HCV is crucial for developing effective treatments.
Purpose of the Study:
- To evaluate antibody and peripheral blood mononuclear cell (PBMC) proliferative responses against HCV antigens in chronically infected patients.
- To investigate the correlation between immune responses and liver damage.
Main Methods:
- Paired serum and PBMC samples were collected from 34 HCV-infected individuals over six months.
- Enzyme-linked immunosorbent assay (ELISA) and carboxyfluorescein succinimidyl ester staining were used to assess antibody and cellular responses.
Main Results:
- Over 70% of patients exhibited specific IgG and IgM against HCV capsid, E1, and NS3 antigens.
- A significant increase in anti-capsid IgM and IgG, and IgA against capsid and NS3, was observed over six months.
- IgA reactivity to structural antigens correlated positively with hepatic damage.
- Cellular immune responses (CD4+ and CD8+ T cells) were generally weak, with poor recognition of the capsid antigen.
Conclusions:
- Chronic HCV infection is characterized by a robust humoral immune response and a limited cellular immune response.
- The correlation between IgA and hepatic damage may hold diagnostic significance, requiring further investigation.
Aim:
In the present study, antibody and peripheral blood mononuclear cells (PBMC) proliferative responses against hepatitis C virus (HCV) antigens were evaluated in HCV chronically infected patients.
Methods:
Paired serum and PBMC samples were taken six months apart from 34 individuals, either treated or not, and tested by enzyme-linked immunosorbent assay (ELISA) and carboxyfluorescein succinimidyl ester staining.
Results:
Over 70% of the patients showed specific IgG and IgM against capsid, E1 and NS3, while HVR-1 was recognized by half of the patients. An increase in the levels of the anti-capsid IgM (P = 0.027) and IgG (P = 0.0006) was observed in six-month samples, compared to baseline. Similarly, a significantly higher percent of patients had detectable IgA reactivity to capsid (P = 0.017) and NS3 (P = 0.005) after six months, compared to baseline. Particularly, IgA against structural antigens positively correlated with hepatic damage (P = 0.036). IgG subclasses evaluation against capsid and NS3 revealed a positive recognition mediated by IgG1 in more than 80% of the individuals. On the contrary, less than 30% of the patients showed a positive proliferative response either of CD4+ or CD8+ T cells, being the capsid poorly recognized.
Conclusion:
These results confirm that while the cellular immune response is narrow and weak, a broad and vigorous humoral response occurs in HCV chronic infection. The observed correlation between IgA and hepatic damage may have diagnostic significance, although it warrants further confirmation.
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