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X连锁免疫球蛋白缺陷伴IgM正常或升高(HIGMX-1)中CD40配体的缺失。

Deletions in the ligand for CD40 in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1).

作者信息

Ramesh N, Fuleihan R, Ramesh V, Lederman S, Yellin M J, Sharma S, Chess L, Rosen F S, Geha R S

机构信息

Division of Immunology, Children's Hospital, Boston, MA 02115.

出版信息

Int Immunol. 1993 Jul;5(7):769-73. doi: 10.1093/intimm/5.7.769.

Abstract

Patients with X-linked Ig deficiency with normal or elevated IgM (HIGMX-1) fail to switch from IgM/IgD to other Ig isotypes. Interaction between the B cell antigen CD40 and the CD40 ligand expressed on activated T cells is critical for T cell driven isotype switching. We have reported that T lymphocytes from three unrelated male patients with HIGMX-1 failed to express CD40 ligand on their surface, but the mRNA for CD40 ligand was of an apparently normal size and level. Analysis of CD40 ligand cDNA from two of the patients revealed deletions that alter the reading frame. Patient 1 displayed two mutations: a C-->A transversion at nucleotide 590 and the deletion of an adjacent C nucleotide. The second patient had a 58 bp deletion from nucleotides 289-346. Furthermore, neither patient expressed a protein product detectable by the CD40L mAb, 5c8.

摘要

患有X连锁免疫球蛋白缺乏伴IgM正常或升高(HIGMX-1)的患者无法从IgM/IgD转换为其他免疫球蛋白同种型。B细胞抗原CD40与活化T细胞上表达的CD40配体之间的相互作用对于T细胞驱动的同种型转换至关重要。我们曾报道,三名无关的患有HIGMX-1的男性患者的T淋巴细胞未能在其表面表达CD40配体,但CD40配体的mRNA大小和水平明显正常。对其中两名患者的CD40配体cDNA分析显示存在改变阅读框的缺失。患者1表现出两个突变:核苷酸590处的C→A颠换以及相邻C核苷酸的缺失。第二名患者在核苷酸289 - 346处有58 bp的缺失。此外,两名患者均未表达可被CD40L单克隆抗体5c8检测到的蛋白质产物。

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