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在单细胞水平上,T细胞受体与主要组织相容性复合体II类-肽复合物的结合会导致抗原无反应性(无反应状态)的诱导。

Binding of T cell receptor to major histocompatibility complex class II-peptide complexes at the single-cell level results in the induction of antigen unresponsiveness (anergy).

作者信息

Celis E, Saibara T

机构信息

First Department of Internal Medicine, Kochi Medical School.

出版信息

Eur J Immunol. 1992 Dec;22(12):3127-34. doi: 10.1002/eji.1830221215.

Abstract

Using dispersion cultures performed in semi-solid medium we demonstrate here that the interaction of T cell antigen receptor molecules with Ia-peptide complexes on the same cell surface results in T cell activation, without the production of lymphokines. This recognition of antigen at the single-cell level, induced a state of anergy which was not due to a decrease of surface T cell antigen receptor/CD3 complexes. The induction of anergy by peptide could not be prevented by the addition of various co-stimulatory signals, including antibodies to CD28, or CD2, high doses of interleukin-2 or phorbol ester.

摘要

我们在此证明,利用在半固体培养基中进行的分散培养,同一细胞表面上的T细胞抗原受体分子与Ia-肽复合物相互作用会导致T细胞活化,而不会产生淋巴因子。这种在单细胞水平上对抗原的识别诱导了一种无反应状态,这并非由于表面T细胞抗原受体/CD3复合物减少所致。添加各种共刺激信号,包括抗CD28或CD2抗体、高剂量白细胞介素-2或佛波酯,都无法阻止肽诱导的无反应状态。

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