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使用I-A突变小鼠品系B6.C-H-2bm12对选定Ia决定簇的T细胞应答。

T cell responses to select Ia determinants using the I-A mutant mouse strain B6.C-H-2bm12.

作者信息

Skelly R R, Pappas F, Koprak S, Ahmed A, Hansen T H

出版信息

J Immunol. 1982 Nov;129(5):2094-7.

PMID:6181160
Abstract

The T cell repertoire of B6.C-H-2bm12 mice (an I-A mutant mouse strain) to wild-type Iab antigens was investigated using both secondary proliferative cultures and cloned T cell lines. Because bm12 mice have a gain-loss mutation of their gene encoding the Ia beta-chain polypeptide, bm12 anti-B6 T cell responses are specific for the select component of Iab specificities that was lost as a result of the mutation. Although stimulator cells bearing Iab antigens elicited the strongest responses, Iaq, d, and s antigens also resulted in reproducible stimulations of these bm12 anti-B6-primed T cells. Cloned T cell lines isolated from bm12 anti-b6 cultures revealed similar findings, with most clones recognizing determinants unique for Iab antigens; however, clones showing cross-reactions with Iad and/or q were also selected. Using F1 hybrid responder T cells (mutant x cross-reactive strain), we further dissected this cross-reactivity into several distinct cross-reactive determinants. Because bm12 mice lack the serologically defined Ia differentiation antigen W39, T cell recognition of this determinant was investigated by using bm12 anti-B6-primed cells. Stimulation by Ia.W39+ cells was appreciably better than by Ia.W39- (Xid-defective) cells, suggesting that bm12 T cells recognize an Xid-regulated, W39-like Ia differentiation antigen.

摘要

利用二次增殖培养和克隆的T细胞系,研究了B6.C-H-2bm12小鼠(一种I-A突变小鼠品系)针对野生型Iab抗原的T细胞库。由于bm12小鼠编码Iaβ链多肽的基因存在得失突变,bm12抗B6 T细胞反应对因突变而丢失的Iab特异性的选择成分具有特异性。尽管携带Iab抗原的刺激细胞引发了最强的反应,但Iaq、d和s抗原也能对这些经bm12抗B6致敏的T细胞产生可重复的刺激。从bm12抗B6培养物中分离出的克隆T细胞系也有类似的发现,大多数克隆识别Iab抗原特有的决定簇;然而,也筛选出了与Iad和/或q有交叉反应的克隆。使用F1杂种反应性T细胞(突变体x交叉反应性品系),我们进一步将这种交叉反应性细分为几个不同的交叉反应决定簇。由于bm12小鼠缺乏血清学定义的Ia分化抗原W39,因此利用经bm12抗B6致敏的细胞研究了该决定簇的T细胞识别。Ia.W39+细胞的刺激明显优于Ia.W39-(Xid缺陷)细胞,这表明bm12 T细胞识别一种Xid调节的、W39样的Ia分化抗原。

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