Biologics and JAK inhibitors for the treatment of monogenic systemic autoinflammatory diseases in children

被引:9
|
作者
Du, Yan [1 ,2 ]
Liu, Meng [1 ,3 ]
Nigrovic, Peter A. [1 ,4 ]
Dedeoglu, Fatma [1 ]
Lee, Pui Y. [1 ,5 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Div Immunol, Boston, MA USA
[2] Zhejiang Univ, Dept Rheumatol, Affiliated Hosp 2, Sch Med, Hangzhou, Peoples R China
[3] Guangdong Second Prov Gen Hosp, Dept Rheumatol & Immunol, Guangzhou, Peoples R China
[4] Harvard Med Sch, Brigham & Womens Hosp, Div Rheumatol Inflammat & Immun, Boston, MA USA
[5] Harvard Med Sch, Boston Childrens Hosp, Div Immunol, 1 Blackfan Circle,Karp RB 10th Floor, Boston, MA 02115 USA
基金
美国国家卫生研究院; 新加坡国家研究基金会;
关键词
Systemic autoinflammatory disease; autoinflammation; inflammasome; interferon; NF-KB; IL-1; TNF; biologics; JAK inhibitors; NF-KAPPA-B; INTERLEUKIN-1 RECEPTOR ANTAGONIST; CONTROLLED-TRIAL; TNF RECEPTOR; DEFICIENCY; MUTATIONS; INFLAMMATION; PHENOTYPE; ARTHRITIS; EFFICACY;
D O I
10.1016/j.jaci.2022.12.816
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Systemic autoinflammatory diseases (SAIDs) are caused by aberrant activation of 1 or more inflammatory pathways in an antigen-independent manner. Monogenic forms of SAIDs typically manifest during childhood, and early treatment is essential to minimize morbidity and mortality. On the basis of the mechanism of disease and the dominant cytokine(s) that propagates inflammation, monogenic SAIDs can be grouped into major categories including inflammasomopathies/disorders of IL-1, interferonopathies, and disorders of nuclear factor-KB and/or aberrant TNF activity. This classification scheme has direct therapeutic relevance given the availability of biologic agents and small-molecule inhibitors that specifically target these pathways. Here, we review the experience of using biologics that target IL-1 and TNF as well as using Janus kinase inhibitors for the treatment of monogenic SAIDs in pediatric patients. We provide an evidence-based guide for the use of these medications and discuss their mechanism of action, safety profile, and strategies for therapeutic monitoring. (J Allergy Clin Immunol 2023;151:607-18.)
引用
收藏
页码:607 / 618
页数:12
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