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人细胞毒性淋巴细胞。V. 由同种异体或自体刺激细胞激活的γδ+细胞毒性淋巴细胞前体的频率和特异性。

Human cytotoxic lymphocytes. V. Frequency and specificity of gamma delta+ cytotoxic lymphocyte precursors activated by allogeneic or autologous stimulator cells.

作者信息

Kabelitz D, Bender A, Schondelmaier S, da Silva Lobo M L, Janssen O

机构信息

Institute of Immunology, University of Heidelberg, West Germany.

出版信息

J Immunol. 1990 Nov 1;145(9):2827-32.

PMID:2120339
Abstract

We have investigated the frequency and specificity of gamma delta+ cytotoxic lymphocyte precursors (CLP) under limiting dilution culture conditions. E rosette separated total T cells and CD3+CD4-CD8-TCR alpha beta- double-negative (DN) T cells were cocultured with allogeneic or autologous PBMC stimulator cells, and frequencies of alloreactive and autoreactive CLP were determined after 12 to 14 days against Con A blast target cells. Freshly isolated DN cells consisting of 82.3 +/- 8.2% gamma delta+ T cells did not exert cytolytic activity against K562 or anti-TCR gamma delta mAb-producing hybridoma cells. In striking contrast to E+ cells, the vast majority of alloantigen-stimulated clonally developing DN CLP did not show specificity for stimulator-derived target cells. Thus, frequencies of alloreactive and autoreactive CLP after alloantigenic stimulation were in the range of 1/100 to 1/4800 and 1/450 to 1/5000, respectively. After coculture with autologous stimulator cells, frequencies of autoreactive and alloreactive DN CLP were 1/700 to 1/2700 and 1/1360 to 1/4500, respectively. Split culture analysis revealed that most proliferating DN colonies selected for high probability of clonality simultaneously killed both autologous and HLA-mismatched allogeneic targets. The majority of the DN cells expressed the CD3+/TCR gamma delta+ phenotype after culture, and thus were not CD2+CD3- NK cells. Taken together, our results show that 1) freshly isolated peripheral blood gamma delta+ T cells lack cytotoxic activity, and 2) most cytotoxic gamma delta+ T cells activated by autologous or allogeneic stimulator cells under limiting dilution conditions do not discriminate between autologous and allogeneic targets.

摘要

我们在有限稀释培养条件下研究了γδ+细胞毒性淋巴细胞前体(CLP)的频率和特异性。通过E花环分离总T细胞,并将CD3+CD4-CD8-TCRαβ-双阴性(DN)T细胞与同种异体或自体PBMC刺激细胞共培养,在12至14天后针对Con A刺激的靶细胞测定同种异体反应性和自身反应性CLP的频率。新鲜分离的由82.3±8.2%γδ+ T细胞组成的DN细胞对K562或产生抗TCRγδ单克隆抗体的杂交瘤细胞不具有细胞溶解活性。与E+细胞形成鲜明对比的是,绝大多数经同种异体抗原刺激的克隆性发育的DN CLP对刺激物来源的靶细胞没有特异性。因此,同种异体抗原刺激后同种异体反应性和自身反应性CLP的频率分别在1/100至1/4800和1/450至1/5000范围内。与自体刺激细胞共培养后,自身反应性和同种异体反应性DN CLP的频率分别为1/700至1/2700和1/1360至1/4500。分割培养分析显示,大多数因克隆性高概率而选择的增殖性DN集落同时杀死自体和HLA不匹配的同种异体靶细胞。培养后大多数DN细胞表达CD3+/TCRγδ+表型,因此不是CD2+CD3-NK细胞。综上所述,我们的结果表明:1)新鲜分离的外周血γδ+ T细胞缺乏细胞毒性活性;2)在有限稀释条件下,由自体或同种异体刺激细胞激活的大多数细胞毒性γδ+ T细胞不能区分自体和同种异体靶细胞。

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