Systemic lupus erythematosus and immunodeficiency

被引:5
作者
Chan, Shirley Chiu Wai [1 ]
Lau, Chak Sing [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Div Rheumatol & Clin Immunol, Hong Kong, Peoples R China
来源
RHEUMATOLOGY AND IMMUNOLOGY RESEARCH | 2021年 / 2卷 / 03期
关键词
immunodeficiency; infections; systemic lupus erythematosus; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; CHRONIC GRANULOMATOUS-DISEASE; MYCOPHENOLATE-MOFETIL; ANTI-C1Q ANTIBODIES; SERIOUS INFECTIONS; NEPHRITIS; THERAPY; RISK; RITUXIMAB; SAFETY;
D O I
10.2478/rir-2021-0019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease caused by a combination of genetic, epigenetic, and environmental factors. Recent advances in genetic analysis coupled with better understanding of different immune regulatory and signaling pathways have revealed the complex relationship between autoimmunity, including SLE, and immunodeficiency. Furthermore, the expanding therapeutic armamentarium has led to the increasing awareness of secondary immunodeficiency in these patients. This article serves to update the current understanding of SLE and immunodeficiency by discussing the shared genetic factors and immunobiology. We also summarize the effects of immunosuppressive therapies with a focus on secondary antibody deficiency (SAD) after B-cell targeted therapies.
引用
收藏
页码:131 / 138
页数:8
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