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Peripheral blood memory B cells are resistant to apoptosis in chronic hepatitis C patients
Toshiaki Mizuochi1, Masahiko Ito, Kenji Takai
1Department of Research on Blood and Biological Products, 4-7-1 Gakuen, Musashi-Murayama, Tokyo 208-0011, Japan. miz@nih.go.jp
Insights
In chronic hepatitis C (CHC) patients, CD27(+) B cells, a memory phenotype, are surprisingly resistant to apoptosis. This suggests memory B cells may serve as a reservoir for persistent hepatitis C virus (HCV) infection.
Area of Science:
- Immunology
- Virology
- Hepatology
Background:
- Peripheral B cells in chronic hepatitis C (CHC) patients are infected with hepatitis C virus (HCV).
- A reduced frequency of CD27(+) B cells (memory phenotype) was observed in CHC patients.
- It was hypothesized that CD27(+) B cells are susceptible to apoptosis upon HCV infection.
Purpose of the Study:
- To analyze the susceptibility of CD27(+) B cells to apoptosis in CHC patients.
- To investigate the role of memory B cells in persistent HCV infection.
Main Methods:
- Analysis of apoptosis in CD27(+) and CD27(-) B cell subsets from CHC patients.
- Comparison of apoptosis resistance between B cell subsets.
Main Results:
- Contrary to the initial assumption, CD27(+) B cells demonstrated increased resistance to apoptosis compared to CD27(-) B cells.
- This finding challenges the notion that memory B cells are readily eliminated.
Conclusions:
- CD27(+) B cells are more resistant to apoptosis than CD27(-) B cells in CHC patients.
- This resistance suggests a potential role for memory B cells as a reservoir for persistent HCV infection.
- Further research is warranted to elucidate the mechanisms behind memory B cell survival and their contribution to chronic infection.
Abstract:
Our recent study indicated that peripheral B cells in chronic hepatitis C (CHC) patients were infected with hepatitis C virus (HCV). It was also demonstrated that the frequency of CD27(+) B cells, i.e. memory phenotype, was significantly reduced in the peripheral blood of CHC patients. An assumption was made by these findings that the CD27(+) B cells are susceptible to apoptosis when infected with HCV. Therefore, in this study, the susceptibility of CD27(+) B cells to apoptosis in CHC patients was analyzed. Contrary to our assumption, it was found that CD27(+) B cells are more resistant to apoptosis than the counterpart subset, i.e. CD27(-) B cells. The rationale for this finding is discussed with regard to the possible role for memory B cells as an HCV reservoir for persistent infection in CHC patients.
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