Immune reconstitution following autologous transfers of CD3/CD28 stimulated CD4+ T cells to HIV-infected persons

被引:25
作者
Bernstein, WB
Cox, JH
Aronson, NE
Tracy, LR
Schlienger, K
Ratto-Kim, S
Garner, R
Cotte, J
Zheng, ZH
Winestone, L
Liebig, C
Galley, LM
Connors, M
Birx, DL
Carroll, RG
Levine, BL [1 ]
机构
[1] Univ Penn, Ctr Canc, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Walter Reed Army Inst Res, Div Retrovirol, Rockville, MD 20850 USA
[3] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
[4] Natl Naval Med Ctr, Bethesda, MD 20889 USA
[5] Henry M Jackson Fdn, Rockville, MD 20850 USA
[6] Walter Reed Army Med Ctr, Washington, DC 20307 USA
[7] US FDA, Ctr Drug Evaluat & Res, Rockville, MD 20857 USA
[8] NIAID, Bethesda, MD 20892 USA
关键词
HIV; adoptive transfer; immune reconstitution; immunotherapy; ELISpot; TCR V beta; CD28;
D O I
10.1016/j.clim.2004.03.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have previously shown that adoptive transfer of in vitro CD3/CD28 activated autologous CD4(+) T cells results in increased CD4 counts and CD4/CD8 ratios in HIV+ subjects. In this report, analysis of variable beta (Vbeta) chain T cell receptor (TCR) repertoire showed that CD3/ CD28 stimulation was able to increase polyclonality within skewed spectra types in vitro. In vivo, two of eight subjects showed increase in TCR diversity and importantly, in no subject did a highly skewed in vivo repertoire emerge. Measurement of proliferative response to alloantigen showed increases following infusions. Response to pharmacological stimulus and lectin via Interferon-gamma ELISpot assay showed increases in a subset of subjects following infusions. However, interferon-gamma response to HIV antigens and peptides declined concurrent with stable or diminishing latent infectious viral load in CD4(+) T cells. These data provide further evidence that adoptive transfer of activated autologous CD4(+) T cells can augment the immune system. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:262 / 274
页数:13
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