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迟发型抑制性T细胞活性的抗原介导

Antigen mediation of a late-acting suppressor T-cell activity.

作者信息

Warren R W, Davie J M

出版信息

J Exp Med. 1977 Dec 1;146(6):1627-39. doi: 10.1084/jem.146.6.1627.

Abstract

Carrier-specific suppressor T cells can suppress antibody secretion by high avidity IgG plaque-forming cells (PFC) within 90 min in vitro. This process can be blocked by the inclusion of soluble carrier in the cell mixture or by the exposure of target cells to anti-carrier antibodies or pronase. Moreover, suppression can be augmented by PFC exposure to the soluble hapten-carrier conjugate. Finally, carrier specificity may be overcome by preincubation of the target population with a hapten-heterologous carrier before addition of heterologous carrier ATC. Thus, it is likely that high avidity suppression depends upon immunogen bound to the surfaces of antibody-secreting cells which serves as a target for suppressor cells or molecules.

摘要

载体特异性抑制性T细胞可在体外90分钟内抑制高亲和力IgG噬斑形成细胞(PFC)的抗体分泌。在细胞混合物中加入可溶性载体,或使靶细胞暴露于抗载体抗体或链霉蛋白酶,均可阻断这一过程。此外,PFC暴露于可溶性半抗原-载体偶联物可增强抑制作用。最后,在加入异源载体ATC之前,用半抗原-异源载体对靶细胞群体进行预孵育,可克服载体特异性。因此,高亲和力抑制作用可能取决于与抗体分泌细胞表面结合的免疫原,而该免疫原可作为抑制细胞或分子的靶标。

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