2B4+ CD8+ T cells play an inhibitory role against constrained HIV epitopes

被引:16
作者
Aldy, Kim N. [1 ,2 ]
Horton, Nathan C. [1 ]
Mathew, Porunelloor A. [1 ]
Mathew, Stephen O. [1 ]
机构
[1] Univ N Texas, Hlth Sci Ctr, Dept Mol Biol & Immunol, Ft Worth, TX 76107 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Surg Burn Trauma Crit Care, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Cytotoxic T lymphocyte (CTL); Cell surface receptor; 2B4; HIV epitopes; B lymphoblastoid cell line (BLCL); NATURAL-KILLER-CELLS; HIV-1-INFECTED PATIENTS; CUTTING EDGE; RECEPTOR; EXPRESSION; PROTEIN; CD244; ACTIVATION; RESPONSES; MOLECULE;
D O I
10.1016/j.bbrc.2011.01.062
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytotoxic T cells play a critical role in the control of HIV and the progression of infected individuals to AIDS. 2B4 (CD244) is a member of the SLAM family of receptors that regulate lymphocyte development and function. The expression of 2B4 on CD8(+) T cells was shown to increase during AIDS disease progression. However, the functional role of 2B4(+) CD8(+) T cells against HIV infection is not known. Here, we have examined the functional role of 2B4(+) CD8(+) T cells during and after stimulation with HLA B14 or B27 restricted HIV epitopes. Interestingly, IFN-gamma secretion and cytotoxic activity of 2B4(+) CD8(+) T cells stimulated with HIV peptides were significantly decreased when compared to influenza peptide stimulated 2B4(+) CD8(+) T cells. The expression of the signaling adaptor molecule SAP was downregulated in 2B4(+) CD8(+) T cells upon HIV peptide stimulation. These results suggest that 2B4(+) CD8(+) T cells play an inhibitory role against constrained HIV epitopes underlying the inability to control the virus during disease progression. Published by Elsevier Inc.
引用
收藏
页码:503 / 507
页数:5
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