HLA-A*2402-restricted HIV-1-specific cytotoxic T lymphocytes and escape mutation after ART with structured treatment interruptions
| Autor: | Junko Tanuma, Masafumi Takiguchi, Yoshimi Kikuchi, Hiroyuki Gatanaga, Natsuo Tachikawa, Hikaru Yamanaka, Saori Matsuoka, Katsuji Teruya, Shinichi Oka, Mamoru Fujiwara |
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| Rok vydání: | 2008 |
| Předmět: |
Immunology
HLA-A24 Antigen HIV Infections medicine.disease_cause Microbiology Virus Epitope Epitopes medicine Humans Cytotoxic T cell Prospective Studies Mutation HLA-A Antigens biology T lymphocyte biology.organism_classification Virology HLA-A CTL Infectious Diseases Anti-Retroviral Agents Lentivirus HIV-1 T-Lymphocytes Cytotoxic |
| Zdroj: | Microbes and Infection. 10:689-698 |
| ISSN: | 1286-4579 |
| Popis: | Although a limited duration of immune activation of structured treatment interruptions (STIs) has been reported, the immune escape mechanism during STIs remains obscure. We therefore investigated the role of three immunodominant cytotoxic T lymphocyte (epitopes) in 12 HLA-A*2402-positive patients participating longitudinally during the clinical study of early antiretroviral treatment (ART) with five series of structured treatment interruptions (STIs). The frequency of HLA-A*2402-restricted CTLs varied widely and a sustained CTL response was rarely noted. However, a Y-to-F substitution at the second position in an immunodominant CTL epitope Nef138-10 (Nef138-2F), which was previously demonstrated as escape mutation, was frequently detected in seven patients primarily and emerged in the remaining five patients thereafter, and the existence of escape mutations was correlated with high pVL levels early in the clinical course. These findings suggest that escape mutation in the immunodominant CTL epitope may be one of the mechanisms to limit HIV-1-specific immune control in STIs. |
| Databáze: | OpenAIRE |
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