Braley-Mullen H
J Immunol. 1986 Nov 1;137(9):2761-7.
Optimally immunogenic amounts of type III pneumococcal polysaccharide (S3) activate a population of contrasuppressor T cells (Tcs), which have been shown to play an important role in the induction of anti-S3 antibody responses. These Tcs belong to a unique T cell subset that has the surface phenotype Lyt 1+2- L3T4- I-J+ I-A+. These Tcs are also cyclophosphamide (Cy)-sensitive and sensitive to antilymphocyte serum (ALS) and mitomycin C. Tcs have antigen-binding receptors, indicating that any interactions of Tcs with B cells or T suppressor cells (Ts) (both of which also have antigen-binding receptors) must be via an antigen bridge rather than an idiotype-anti-idiotype interaction. Tcs are also Igh restricted in their action. Contrasuppression is manifest only when the Tcs are Igh compatible with both the Ts and the responding B cells. Tcs apparently mediate their effects by releasing a soluble factor, since a soluble factor extracted from Tcs is able to abrogate the effects of S3-specific Ts.
最佳免疫原量的III型肺炎球菌多糖(S3)可激活一群反抑制性T细胞(Tcs),已证明这些细胞在抗S3抗体反应的诱导中起重要作用。这些Tcs属于一个独特的T细胞亚群,其表面表型为Lyt 1+2- L3T4- I-J+ I-A+。这些Tcs对环磷酰胺(Cy)敏感,对抗淋巴细胞血清(ALS)和丝裂霉素C也敏感。Tcs具有抗原结合受体,这表明Tcs与B细胞或T抑制细胞(Ts)(两者也都具有抗原结合受体)之间的任何相互作用都必须通过抗原桥而非独特型-抗独特型相互作用。Tcs的作用也受免疫球蛋白重链(Igh)限制。仅当Tcs与Ts及反应性B细胞在Igh上相容时,反抑制作用才会显现。Tcs显然通过释放一种可溶性因子来介导其效应,因为从Tcs中提取的一种可溶性因子能够消除S3特异性Ts的效应。