Selective elimination of human regulatory T lymphocytes in vitro with the recombinant immunotoxin LMB-2

被引:60
作者
Attia, P
Powell, DJ
Maker, AV
Kreitman, RJ
Pastan, I
Rosenberg, SA
机构
[1] NCI, Surg Branch, NIH, Ctr Canc Res, Bethesda, MD 20892 USA
[2] NCI, Mol Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
关键词
human; immunotoxin; LMB-2; CD25; regulatory T cell; depletion; Pseudomonas exotoxin;
D O I
10.1097/01.cji.0000187959.45803.0c
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD4(+)CD25(+) T-regulatory cells (T-reg) can inhibit the proliferation and cytokine secretion of CD4(+)CD25(-) helper T cells in mice and humans. In murine tumor models, the presence of these T-reg cells can inhibit the antitumor effectiveness of T-cell transfer and active immunization approaches. We have thus initiated efforts to eliminate T-reg cells selectively from human peripheral blood mononuclear cells (PBMCs) to potentially bolster antitumor responses. LMB-2 is a recombinant immunotoxin that is a fusion of a single-chain Fv fragment of the anti-Tac anti-CD25 monoclonal antibody to a truncated form of the bacterial Pseudomonas exotoxin A. In vitro incubation of human PBMCs with LMB-2 reduced the levels of CD4(+)CD25(+) and Foxp3-expressing cells without impairing the function of the remaining lymphocytes. The short in vivo half-life of LMB-2 makes it an attractive candidate for reducing human T-reg cells in vivo before the administration of cancer vaccine or cell transfer immunotherapy approaches.
引用
收藏
页码:208 / 214
页数:7
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