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抗IgD抗体对小鼠免疫系统的多克隆激活。XI. 膜IgD交联对体内多克隆抗体应答产生的作用。

Polyclonal activation of the murine immune system by an antibody to IgD. XI. Contribution of membrane IgD cross-linking to the generation of an in vivo polyclonal antibody response.

作者信息

Goroff D K, Holmes J M, Bazin H, Nisol F, Finkelman F D

机构信息

Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814-4799.

出版信息

J Immunol. 1991 Jan 1;146(1):18-25.

PMID:1984444
Abstract

The injection of mice with a foreign, polyclonal antibody to IgD sequentially induces: 1) activation of B cells by cross-linking of their cell membrane (m) IgD; 2) B cell processing and presentation of the bound anti-IgD antibody to T cells; 3) activation of these T cells; and 4) T-dependent stimulation of B cell differentiation into IgG1 secreting cells. To determine whether the cross-linking of B cell membrane IgD and/or the resulting B cell activation that follows contribute to the generation of the polyclonal IgG1 response, we examined the abilities of three sets of anti-delta mAb or mAb fragments to stimulate polyclonal IgG1 production. Within each set mAb were matched for species and Ig isotypic determinants, but differed in avidity for IgD or in ability to cross-link IgD. In addition, experiments were performed to determine whether the anti-delta mAb had to be foreign to the immunized mouse to stimulate an IgG1 response. Results of these experiments indicate that: 1) recognition of the injected anti-delta antibody as foreign is required for the induction of a polyclonal IgG1 response; 2) the cross-linking of B cell membrane Ig, which directly activates B cells, can contribute considerably to the generation of in vivo IgG1 production; and 3) that even relatively weak cross-linking of membrane Ig by ligands that bind it with low avidity can make this contribution.

摘要

给小鼠注射针对IgD的异源多克隆抗体可依次诱导:1)通过其细胞膜(m)IgD的交联激活B细胞;2)B细胞处理并将结合的抗IgD抗体呈递给T细胞;3)这些T细胞的激活;以及4)T细胞依赖性刺激B细胞分化为分泌IgG1的细胞。为了确定B细胞膜IgD的交联和/或随后产生的B细胞激活是否有助于多克隆IgG1反应的产生,我们检测了三组抗δ单克隆抗体(mAb)或mAb片段刺激多克隆IgG1产生的能力。每组中的mAb在物种和Ig同种型决定簇方面相互匹配,但对IgD的亲和力或交联IgD的能力不同。此外,还进行了实验以确定抗δ mAb是否必须与免疫小鼠异源才能刺激IgG1反应。这些实验结果表明:1)诱导多克隆IgG1反应需要将注射的抗δ抗体识别为异源;2)直接激活B细胞的B细胞膜Ig交联可对体内IgG1产生的生成有很大贡献;3)即使是与膜Ig以低亲和力结合的配体对膜Ig进行相对较弱的交联也可做出这种贡献。

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