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Primary Antibody Deficiencies

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Journal Nat Rev Immunol
Date 2013 Jun 15
PMID 23765059
Citations 109
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Abstract

Primary antibody deficiencies (PADs) are the most common inherited immunodeficiencies in humans. The use of novel approaches, such as whole-exome sequencing and mouse genetic engineering, has helped to identify new genes that are involved in the pathogenesis of PADs and has enabled the characterization of the molecular pathways that are involved in B cell development and function. Here, we review the different PADs in terms of their known or putative mechanisms, which can be B cell intrinsic, B cell extrinsic or not defined so far. We also describe the clinical manifestations (including susceptibility to infections, autoimmunity and cancer) that have been associated with the various PADs.

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References
1.
GREENBERG F, Crowder W, Paschall V, Lubianski B, Ledbetter D . Familial DiGeorge syndrome and associated partial monosomy of chromosome 22. Hum Genet. 1984; 65(4):317-9. DOI: 10.1007/BF00291554. View

2.
Jabara H, McDonald D, Janssen E, Massaad M, Ramesh N, Borzutzky A . DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation. Nat Immunol. 2012; 13(6):612-20. PMC: 3362684. DOI: 10.1038/ni.2305. View

3.
Pachlopnik Schmid J, Lemoine R, Nehme N, Cormier-Daire V, Revy P, Debeurme F . Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome"). J Exp Med. 2012; 209(13):2323-30. PMC: 3526359. DOI: 10.1084/jem.20121303. View

4.
Rieux-Laucat F, Hivroz C, Lim A, Mateo V, Pellier I, Selz F . Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency. N Engl J Med. 2006; 354(18):1913-21. DOI: 10.1056/NEJMoa053750. View

5.
Zhou Q, Lee G, Brady J, Datta S, Katan M, Sheikh A . A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency. Am J Hum Genet. 2012; 91(4):713-20. PMC: 3484656. DOI: 10.1016/j.ajhg.2012.08.006. View