HCV‐specific CD27 CD28 memory T cells are depleted in hepatitis C virus and Schistosoma mansoni co‐infection

Immunology - Tập 110 Số 4 - Trang 513-518 - 2003
Mohamed F. El‐Refaei1, Nabila El-Sheikh2, Karim Kamal3, Huyen Cao1
1California Department of Health Services, Richmond, CA, USA
2Faculty of Medicine for Girls, Al Azhar University, Cairo, Egypt, and
3US Naval Medical Research Unit #3 (NAMRU‐3), Cairo, Egypt

Tóm tắt

SummaryFactors 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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