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白细胞介素4对B细胞活性的诱导在体外被一种受体特异性单克隆抗体所抑制。

Induction of B cell activities by interleukin 4 is inhibited by a receptor-specific monoclonal antibody in vitro.

作者信息

Maliszewski C R, Sato T A, Vanden Bos T, Beckmann M P, Grabstein K H

机构信息

Department of Immunology, Immunex Corporation, Seattle, WA 98101.

出版信息

Eur J Immunol. 1990 Aug;20(8):1735-40. doi: 10.1002/eji.1830200817.

Abstract

The effects of interleukin (IL) 4 on B cell growth and differentiation are mediated through binding of IL 4 to a specific cell surface receptor. The murine T cell IL 4 receptor (IL 4R) has recently been cloned and monoclonal antibodies (mAb) which bind specifically to the IL 4R have been developed. The ability of two of these anti-IL 4R mAb (M1 and M2) to inhibit IL 4-induced B cell functions in vitro was examined. The M1 mAb inhibited the ability of IL 4 to induce B cell proliferation in a dose-related fashion. The inhibition was specific for proliferation induced by IL 4 in that the antibody did not affect induction of proliferation by IL 1. Similarly, M1 inhibited IL 4-dependent B cell differentiation as measured by induction of IgG1 and IgE secretion, decreased IgG3 secretion, increased Ia expression, and increased Fc epsilon R (CD23) expression. In contrast, the anti-IL 4R-specific mAb M2 had no effect upon any of these activities. The ability of M1 but not M2 to inhibit IL 4-induced B cell growth and differentiation correlated with the inhibition of binding of radiolabeled IL 4 by M1. These reagents should be valuable tools with which to analyze the involvement of IL 4 in immune responses.

摘要

白细胞介素(IL)4对B细胞生长和分化的作用是通过IL 4与特定细胞表面受体结合来介导的。小鼠T细胞IL 4受体(IL 4R)最近已被克隆,并且已经开发出了能特异性结合IL 4R的单克隆抗体(mAb)。检测了其中两种抗IL 4R单克隆抗体(M1和M2)在体外抑制IL 4诱导的B细胞功能的能力。M1单克隆抗体以剂量相关的方式抑制IL 4诱导B细胞增殖的能力。这种抑制作用对IL 4诱导的增殖具有特异性,因为该抗体不影响IL 1诱导的增殖。同样,M1抑制了通过诱导IgG1和IgE分泌、减少IgG3分泌、增加Ia表达以及增加FcεR(CD23)表达所衡量的IL 4依赖性B细胞分化。相比之下,抗IL 4R特异性单克隆抗体M2对这些活性均无影响。M1而非M2抑制IL 4诱导的B细胞生长和分化的能力与M1对放射性标记的IL 4结合的抑制作用相关。这些试剂对于分析IL 4在免疫反应中的作用应该是有价值的工具。

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