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具有X连锁B淋巴细胞缺陷的小鼠中的免疫球蛋白亚类特异性免疫缺陷

Immunoglobulin subclass-specific immunodeficiency in mice with an X-linked B-lymphocyte defect.

作者信息

Perlmutter R M, Nahm M, Stein K E, Slack J, Zitron I, Paul W E, Davie J M

出版信息

J Exp Med. 1979 Apr 1;149(4):993-8. doi: 10.1084/jem.149.4.993.

Abstract

CBA/N mice express an X-linked deficiency in their antibody response to many bacterial carbohydrates; we have shown recently that these antigens normally elicit antibody responses predominantly of the IgM and IgG3 isotypes. Here we demonstrate that mice, with the CBA/N phenotype have perferential deficiencies of IgM and IgG3 immunoglobulin expression, both when measured in serum and in cells secreting these isotypes, and that this deficiency is only partially corrected by polyclonal activation of B cells. This suggests that CBA/N mice may lack a subpopulation of B cells that contain most of the IgG3 precursors.

摘要

CBA/N小鼠对许多细菌碳水化合物的抗体反应存在X连锁缺陷;我们最近发现,这些抗原通常主要引发IgM和IgG3同种型的抗体反应。在此我们证明,具有CBA/N表型的小鼠在血清和分泌这些同种型的细胞中,IgM和IgG3免疫球蛋白表达均存在选择性缺陷,并且这种缺陷仅通过B细胞的多克隆激活得到部分纠正。这表明CBA/N小鼠可能缺乏包含大多数IgG3前体的B细胞亚群。

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