High Frequencies of Functionally Competent Circulating Tax-Specific CD8+ T Cells in Human T Lymphotropic Virus Type 2 Infection

被引:6
作者
Oliveira, Andre L. A. [1 ]
Hayakawa, Hitoshi [1 ]
Schor, Doris
Leite, Ana Claudia C. B. [3 ]
Espindola, Otavio M.
Waters, Allison [2 ]
Dean, Jonathan [1 ]
Doherty, Derek G. [4 ,5 ]
Araujo, Abelardo Q. -C. [1 ,3 ]
Hall, William W. [1 ]
机构
[1] Univ Coll Dublin, Ctr Res Infect Dis, Dublin 4, Ireland
[2] Univ Coll Dublin, Natl Virus Reference Lab, Dublin 4, Ireland
[3] Fundacao Oswaldo Cruz, Lab Res Neuroinfect, Evandro Chagas Inst Clin Res, Rio De Janeiro, Brazil
[4] Natl Univ Ireland, Cellular Immunol Lab, Dept Biol, Maynooth, Kildare, Ireland
[5] Univ Dublin Trinity Coll, Dept Immunol, St Jamess Hosp, Dublin 2, Ireland
关键词
TROPICAL SPASTIC PARAPARESIS; I PROVIRAL LOAD; VIVO CELLULAR TROPISM; HTLV-I; NEUROLOGIC DISEASE; HLA-B; LYMPHOCYTES; MEMORY; CARRIERS; SUBSETS;
D O I
10.4049/jimmunol.0900508
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human T lymphotropic virus type 2 (HTLV-2) is characterized by a clinically asymptomatic. persistent infection in the vast majority of infected individuals. In this study, we have characterized for the first time ex vivo specific CTL responses against the HTLV-2 Tax protein. We could detect CTL responses only against a single HLA-A*0201-restricted Tax2 epitope, comprising residues 11-19 (LLYGYPVYV), among three alleles screened. Virus-specific CTLs could be detected in most evaluated subjects, with frequencies as high as 24% of circulating CD8(+) T cells. The frequency of specific CTLs had a statistically significant positive correlation with proviral load levels. The majority of virus-specific CD8(+) T cells exhibited an effector memory/terminally differentiated phenotype, expressed high levels of cytotoxicity mediators, including perforin and granzyme B, and lysed in vitro target cells pulsed with Tax2((11-19)) synthetic peptide in a dose-dependent manner. Our findings suggest that a strong, effective CTL response may control HTLV-2 viral burden and that this may be a significant factor in maintaining persistent infection and in the prevention of disease in infected individuals. The Journal of Immunology, 2009, 183: 2957-2965.
引用
收藏
页码:2957 / 2965
页数:9
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