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東京大学医科学研究所
学友会セミナーのお知らせ

開催日時: 平成17年7月12日(火)
       16:00~17:00

開催場所: 東京大学医科学研究所附属病院8階 トミーホール(南会議室)
(地下鉄南北線白金台駅下車。本館の裏の新病院棟8階です。)

講 師: Javier Martinez-Picado Ph.D.

所 属: Retrovirology Laboratory Hospital “Germans Trias i Pujol”
Universitat Aut_noma de Barcelona

演 題: HIV evolution: CTL escape mutation and reversion after transmission

概  要: Within-patient HIV evolution reflects the strong selection pressure driving viral escape from cytotoxic T-lymphocyte (CTL) recognition.
Whether this intrapatient accumulation of escape mutations translates into HIV evolution at the population level has not been evaluated. We studied over 300 patients drawn from the B- and C-clade epidemics&s_comma; focusing on human leukocyte antigen (HLA) alleles HLA-B57 and HLA-B5801&s_comma; which are associated with long-term HIV control and are therefore likely to exert strong selection pressure on the virus. The CTL response dominating acute infection in HLA-B57/5801-positive subjects drove positive selection of an escape mutation that reverted to wild-type after transmission to HLA-B57/5801-negative individuals&s_comma; suggesting that this CTL escape inflicts a significant cost to viral replicative capacity. A second escape mutation within the epitope&s_comma; by contrast&s_comma; was maintained after transmission. These data show that the process of accumulation of escape mutations within HIV is not inevitable. Complex epitope- and residue-specific selection forces&s_comma; including CTL-mediated positive selection pressure and virus-mediated purifying selection&s_comma; operate in tandem to shape HIV evolution at the population level.
A new mechanism of CTL escape has also been defined during the process of studying CTL-escape mutants in Gag p24. Mutations within CTL epitopes impair T-cell recognition&s_comma; but escape mutations arising in regions flanking epitopes can also alter antigen processing. In HLA-B57+&s_comma; HIV-infected persons&s_comma; immune selection pressure leads to a mutation from alanine to proline at Gag residue 146 immediately preceding the N-terminus of a dominant HLA-B57-restricted epitope. The A146P mutation prevented N-terminal trimming of the optimal epitope by the ER-aminopeptidase ERAP1. These results demonstrate that allele-associated sequence variation within the flanking region of CTL epitopes can alter antigen processing. Identifying such mutations is of major relevance for selection of vaccine sequences.

世話人  ○感染症分野    岩本愛吉
ウィルス感染分野 河岡義裕

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渡辺 すみ子
東京大学医科学研究所再生基礎医科学寄付研究部門
Phone 03-5449-5663/5664



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