简短报告：患有主要组织相容性复合体II类缺陷但具有诱导性免疫反应的双胞胎男孩 - Suppr

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超能文献

Brief report: twin boys with major histocompatibility complex class II deficiency but inducible immune responses.

作者信息

Wolf H M, Hauber I, Gulle H, Thon V, Eggenbauer H, Fischer M B, Fiala S, Eibl M M

机构信息

Institute of Immunology, University of Vienna, Austria.

出版信息

N Engl J Med. 1995 Jan 12;332(2):86-90. doi: 10.1056/NEJM199501123320204.

DOI:10.1056/NEJM199501123320204

PMID:7990905

Abstract

摘要

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Brief report: twin boys with major histocompatibility complex class II deficiency but inducible immune responses.简短报告：患有主要组织相容性复合体II类缺陷但具有诱导性免疫反应的双胞胎男孩

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Decoding Immunobiology Through Genetic Errors of Immunity.通过免疫遗传错误解码免疫生物学

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Splicing defect in RFXANK results in a moderate combined immunodeficiency and long-duration clinical course.RFXANK中的剪接缺陷导致中度联合免疫缺陷和病程延长。

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Genetic evidence for a new type of major histocompatibility complex class II combined immunodeficiency characterized by a dyscoordinate regulation of HLA-D alpha and beta chains.一种新型主要组织相容性复合体II类联合免疫缺陷的遗传学证据，其特征为HLA-Dα链和β链的失调调节。

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Molecular characterization of major histocompatibility complex class II gene expression and demonstration of antigen-specific T cell response indicate a new phenotype in class II-deficient patients.主要组织相容性复合体II类基因表达的分子特征及抗原特异性T细胞反应的证实表明II类缺陷患者存在一种新的表型。

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