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载体特异性B细胞在抗原特异性T细胞替代因子的产生中发挥作用。

Carrier-specific B cells play a role in the production of an antigen-specific T-cell-replacing factor.

作者信息

Kirov S M, Parish C R

出版信息

Scand J Immunol. 1976;5(10):1155-62.

PMID:65005
Abstract

An in vitro anti-hapten response to dinitrophenylated monomeric flagellin (DNP-MON) was used to examine the ability of T cells to collaborate with B cells across a cell-impermeable Millipore membrane. It was found that T cells alone were not able to collaborate with B cells across the membrane. However, B and T cells together produced a T-cell-replacing factor that passed through the membrane and partially restored the antibody response of B cells cultured beneath the membrane. Production of the factor was abolished when carrier-specific B cells were inactivated by [125I]polymeric flagellin (POL) suicide. The T-cell-replacing factor was shown to be nondialysable and antigen-specific. It was also demonstrated that macrophages were required for production of the specific T-cell-replacing factor but that the action of the factor on B cells macrophage-independent.

摘要

利用对二硝基苯基化单体鞭毛蛋白(DNP-MON)的体外抗半抗原反应,来检测T细胞与B细胞跨越细胞不可渗透的微孔膜协同作用的能力。结果发现,单独的T细胞无法跨越该膜与B细胞协同作用。然而,B细胞和T细胞共同产生了一种可穿过该膜的T细胞替代因子,部分恢复了培养在膜下方的B细胞的抗体反应。当载体特异性B细胞被[125I]聚合鞭毛蛋白(POL)自杀法灭活时,该因子的产生被消除。该T细胞替代因子被证明是不可透析的且具有抗原特异性。还证明,产生特异性T细胞替代因子需要巨噬细胞,但该因子对B细胞的作用不依赖巨噬细胞。

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