Variable patterns of programmed death-1 expression on fully functional memory T cells after spontaneous resolution of hepatitis C virus infection

被引:34
作者
Bowen, David G. [1 ]
Shoukry, Naglaa H. [2 ,3 ]
Grakoui, Arash [4 ]
Fuller, Michael J. [1 ]
Cawthon, Andrew G. [1 ]
Dong, Christine [9 ]
Hasselschwert, Dana L. [5 ]
Brasky, Kathleen M. [6 ]
Freeman, Gordon J. [7 ]
Seth, Nilufer P. [8 ]
Wucherpfernnig, Kai W. [8 ]
Houghton, Michael [9 ]
Walker, Christopher M. [1 ,10 ]
机构
[1] Nationwide Childrens Hosp, Res Inst, Ctr Vaccines & Immun, Columbus, OH 43205 USA
[2] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal Hosp Ctr, Montreal, PQ, Canada
[4] Emory Univ, Atlanta, GA 30322 USA
[5] New Iberia Res Ctr, New Iberia, LA USA
[6] SW Fdn Biomed Res, San Antonio, TX 78284 USA
[7] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[8] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[9] Novartis Corp, Emeryville, CA USA
[10] Ohio State Univ, Coll Med & Publ Hlth, Columbus, OH 43210 USA
关键词
D O I
10.1128/JVI.00060-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:5109 / 5114
页数:6
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