T-helper-2 cells and atopic disease: lessons learnt from inborn errors of immunity

被引:4
|
作者
Ma, Cindy S. [1 ,2 ,3 ]
机构
[1] Garvan Inst Med Res, Sydney, NSW, Australia
[2] UNSW Sydney, Fac Med & Hlth, Sch Clin Med, Sydney, NSW, Australia
[3] Clin Immunogen Res Consortium Australasia CIRCA, Darlinghurst, Australia
基金
英国医学研究理事会;
关键词
OF-FUNCTION MUTATIONS; T-CELLS; COMBINED IMMUNODEFICIENCY; IL-9-PRODUCING CELLS; SIGNAL TRANSDUCER; AORTIC-ANEURYSMS; ALLERGIC DISEASE; IGE; DEFICIENCY; TRANSCRIPTION;
D O I
10.1016/j.coi.2023.102298
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inborn errors of immunity (IEI) are caused by monogenic variants that affect the host response to bacterial, viral, and fungal pathogens. As such, individuals with IEI often present with severe, recurrent, and life-threatening infections. However, the spectrum of disease due to IEI is very broad and extends to include autoimmunity, malignancy, and atopic diseases such as eczema, atopic dermatitis, and food and environmental allergies. Here, I review IEI that affect cytokine signaling pathways that dysregulate CD4+ T-cell differentiation, resulting in increased T-helper-2 (Th2) cell development, function, and pathogenicity. These are elegant examples of how rare IEI can provide unique insights into more common pathologies such as allergic disease that are impacting the general population at increased frequency. © 2023 Elsevier Ltd
引用
收藏
页数:12
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