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HCV-specific CD27- CD28- memory T cells are depleted in hepatitis C virus and Schistosoma mansoni co-infection
被引:24
作者:

Elrefaei, M
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机构: Calif Dept Hlth Serv, Richmond, CA 94804 USA

El-sheikh, N
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机构: Calif Dept Hlth Serv, Richmond, CA 94804 USA

Kamal, K
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h-index: 0
机构: Calif Dept Hlth Serv, Richmond, CA 94804 USA

Cao, H
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机构: Calif Dept Hlth Serv, Richmond, CA 94804 USA
机构:
[1] Calif Dept Hlth Serv, Richmond, CA 94804 USA
[2] Al Azhar Univ, Fac Med Girls, Cairo, Egypt
[3] USN, Med Res Unit 3, Cairo, Egypt
来源:
关键词:
D O I:
10.1111/j.1365-2567.2003.01769.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Factors that influence the generation and maintenance of memory CD8(+) T cells are not fully understood. The homeostasis of memory T cells is highly dynamic and tightly regulated by various stimuli, including cytokines and antigen-major histocompatibility complex ligands. We characterized the hepatitis C virus (HCV)-specific CD8(+) T-cell responses in a cohort of HCV-infected individuals with or without Schistosoma mansoni co-infection from Egypt. We observed a significantly decreased CD27(-) CD28(-) (late differentiated) memory T-cell population in the HCV co-infected individuals compared to those with HCV infection alone. In contrast, there was no significant difference in the CD27(+) CD28(+) (early differentiated) memory T cells between the two groups. Analysis of human cytomegalovirus-specific CD8(+) T-cell responses in the same individuals failed to reveal a similar pattern of altered memory T-cell differentiation. Thus, S. mansoni co-infection targets a specific subset of memory CD8(+) T cells in HCV infection.
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页码:513 / 518
页数:6
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