Managing comorbid complications in patients with common variable immunodeficiency

被引:7
|
作者
Ballow, Mark [1 ,2 ,3 ]
机构
[1] Women & Childrens Hosp Buffalo, Div Allergy & Immunol, Buffalo, NY 14222 USA
[2] SUNY Buffalo, Sch Med, Buffalo, NY 14260 USA
[3] Univ S Florida, Dept Pediat, Childrens Res Inst, Div Allergy & Immunol, St Petersburg, FL 33701 USA
关键词
SELECTIVE IGA DEFICIENCY; MEMORY B-CELLS; GRANULOMATOUS-DISEASE; IMMUNE-DEFICIENCY; DISORDERS; SUSCEPTIBILITY; PHENOTYPES; SUBGROUPS; THERAPY; LINKAGE;
D O I
10.1016/j.anai.2013.06.032
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Objective: To review the literature related to the identification and treatment of secondary complications associated with common variable immunodeficiency (CVID). Data Sources: The databases of PubMed and Ovid MEDLINE were searched for articles pertaining to comorbid conditions occurring in patients with CVID and effective treatment for or management of those conditions. Study Selections: Articles were selected based on their relevance to the focus of this review, with an emphasis on clinical phenotypes and biomarkers that can help identify patients with CVID and a secondary complication and issues related to their clinical management. Results: Noninfective complications have generated a better understanding of the pathogenesis and treatment of CVID by helping to define clinical and immunologic phenotypes of this disease. These clinical phenotypes have been correlated with different survival risks. Conclusion: Emerging and ongoing research on clinical phenotypes and biomarkers of CVID may help identify and better target treatment for patients with CVID who will develop secondary complications. It is hoped that through this improved knowledge of outcomes, more appropriate treatment for patients can be targeted. (C) 2013 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:S6 / S9
页数:4
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