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原发性 B 细胞免疫缺陷病。

Primary B-cell immunodeficiencies.

机构信息

Division of Allergy and Clinical Immunology, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY 10029-6574, United States; The Rockefeller University, Laboratory of Biochemical Genetics and Metabolism, 1230 York Avenue, Box 179, New York, NY 10065, United States.

Division of Allergy and Clinical Immunology, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY 10029-6574, United States.

出版信息

Hum Immunol. 2019 Jun;80(6):351-362. doi: 10.1016/j.humimm.2018.10.015. Epub 2018 Oct 22.

Abstract

Primary B-cell immunodeficiencies refer to diseases resulting from impaired antibody production due to either molecular defects intrinsic to B-cells or a failure of interaction between B-cells and T-cells. Patients typically have recurrent infections and can vary with presentation and complications depending upon where the defect has occurred in B-cell development or the degree of functional impairment. In this review, we describe B-cell specific immune defects categorized by presence or absence of peripheral B-cells, immunoglobulins isotypes and evidence of antibody impairment.

摘要

原发性 B 细胞免疫缺陷是指由于 B 细胞内在的分子缺陷或 B 细胞与 T 细胞相互作用失败而导致抗体产生受损的疾病。患者通常会反复感染,其表现和并发症可因 B 细胞发育过程中缺陷的部位或功能受损的程度而有所不同。在这篇综述中,我们根据外周 B 细胞、免疫球蛋白同种型和抗体功能受损的证据,描述了 B 细胞特异性免疫缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c2/7395616/345cd8c5654f/nihms-1514348-f0001.jpg

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