Details

Autor(en) / Beteiligte

• Allen, Todd M
• Yu, Xu G
• Kalife, Elizabeth T
• Reyor, Laura L
• Lichterfeld, Mathias
• John, Mina
• Cheng, Michael
• Allgaier, Rachel L
• Mui, Stanley
• Frahm, Nicole
• Alter, Galit
• Brown, Nancy V
• Johnston, Mary N
• Rosenberg, Eric S
• Mallal, Simon A
• Brander, Christian
• Walker, Bruce D
• Altfeld, Marcus

Titel

De Novo Generation of Escape Variant-Specific CD8 super(+) T-Cell Responses following Cytotoxic T-Lymphocyte Escape in Chronic Human Immunodeficiency Virus Type 1 Infection

Ist Teil von

• Journal of virology, 2005-10, Vol.79 (20), p.12952-12960

Erscheinungsjahr

2005

Quelle

EZB Electronic Journals Library

Beschreibungen/Notizen

• Human immunodeficiency virus type 1 (HIV-1) evades CD8 super(+) T-cell responses through mutations within targeted epitopes, but little is known regarding its ability to generate de novo CD8 super(+) T-cell responses to such mutants. Here we examined gamma interferon-positive, HIV-1-specific CD8 super(+) T-cell responses and autologous viral sequences in an HIV-1-infected individual for more than 6 years following acute infection. Fourteen optimal HIV-1 T-cell epitopes were targeted by CD8 super(+) T cells, four of which underwent mutation associated with dramatic loss of the original CD8 super(+) response. However, following the G sub(357)S escape in the HLA-A11-restricted Gag sub(349-359) epitope and the decline of wild-type-specific CD8 super(+) T-cell responses, a novel CD8 super(+) T-cell response equal in magnitude to the original response was generated against the variant epitope. CD8 super(+) T cells targeting the variant epitope did not exhibit cross-reactivity against the wild-type epitope but rather utilized a distinct T-cell receptor V beta repertoire. Additional studies of chronically HIV-1-infected individuals expressing HLA-A11 demonstrated that the majority of the subjects targeted the G sub(357)S escape variant of the Gag sub(349-359) epitope, while the wild-type consensus sequence was significantly less frequently recognized. These data demonstrate that de novo responses against escape variants of CD8 super(+) T-cell epitopes can be generated in chronic HIV-1 infection and provide the rationale for developing vaccines to induce CD8 super(+) T-cell responses directed against both the wild-type and variant forms of CD8 epitopes to prevent the emergence of cytotoxic T-lymphocyte escape variants.