Laboratory evaluation of primary immunodeficiencies

被引:75
|
作者
Oliveira, Joao B. [1 ]
Fleisher, Thomas A. [1 ]
机构
[1] NIH, Dept Lab Med, Ctr Clin, Bethesda, MD USA
关键词
Primary immunodeficiency; laboratory assessment; immunologic diagnosis; immunity; AUTOIMMUNE-LYMPHOPROLIFERATIVE-SYNDROME; CHRONIC GRANULOMATOUS-DISEASE; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; FLOW-CYTOMETRY; IMMUNE-DEFICIENCY; CLINICAL FINDINGS; FOLLOW-UP; MUTATIONS; DEFECTS; SUSCEPTIBILITY;
D O I
10.1016/j.jaci.2009.08.043
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Primary immunodeficiencies are congenital disorders caused by defects in different elements of the immune system. Affected patients usually present clinically with recurrent infections, severe infections, or both, as well as autoimmune phenomena that are associated with many of these disorders. Early diagnosis is essential for referral to specialized care centers and the prompt initiation of appropriate therapy. In this article the authors describe a general approach for the investigation of the most common primary immunodeficiencies, outlining the typical clinical symptoms and most appropriate laboratory investigations. (J Allergy Clin Immunol 2010;125:S297-305.)
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页码:S297 / S305
页数:9
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