期刊
JOURNAL OF VIROLOGY
卷 82, 期 10, 页码 5109-5114出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.00060-08
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资金
- NCI NIH HHS [1CO6RR1643-01] Funding Source: Medline
- NCRR NIH HHS [P51 RR000165, 5U42RR15087, U42 RR015087, RR-00165, 1C06RR014491-01, C06 RR014491] Funding Source: Medline
- NIAID NIH HHS [R01 AI070101, AI070101, U19 AI48231, R56 AI070101, F32 AI055193, U19 AI048231] Funding Source: Medline
- PHS HHS [R01 A147367] Funding Source: Medline
The inhibitory receptor programmed death-1 (PD-1) is present on CD8(+) T cells in chronic hepatitis C virus (HCV), but expression patterns in spontaneously resolving infections are incompletely characterized. Here we report that PD-1 was usually absent on memory CD8(+) T cells from chimpanzees with resolved infections, but sustained low-level expression was sometimes observed in the absence of apparent virus replication. PD-1-positive memory T cells expanded and displayed antiviral activity upon reinfection with HCV, indicating conserved function. This animal model should facilitate studies of whether PD-1 differentially influences effector and memory T-cell function in resolved versus persistent human infections.
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