Abstract
Despite readily detectable virus-specific CD8(+) T cells in most HIV-infected patients, immune surveillance is eventually lost, leading to progression to AIDS. Recently developed insights into human T-cell differentiation have been used to study the phenotype of virus-specific T cells in HIV-infected individuals. Based on these results, we propose that failing immune control in human viral infection could be a result of impaired cytotoxic T-lymphocyte (CTL) maturation into fully differentiated effector T cells. Impaired maturation is not confined to HIV-specific CD8(+) T cells but could also be involved in failing immunity to Epstein-Barr virus and other viral infections. We postulate that CD27(-) effector CD8(+) T cells might be required for adequate control of chronic viral infection and prevention of disease development.
| Original language | English |
|---|---|
| Pages (from-to) | 586-91 |
| Number of pages | 6 |
| Journal | Trends in immunology |
| Volume | 23 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - Dec 2002 |
| Externally published | Yes |
Keywords
- CD8-Positive T-Lymphocytes/immunology
- Cell Differentiation
- Epstein-Barr Virus Infections/immunology
- HIV Infections/immunology
- Humans
- Models, Immunological
- T-Lymphocytes, Cytotoxic/immunology
- Tumor Necrosis Factor Receptor Superfamily, Member 7/metabolism
- Virus Diseases/immunology
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