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dc.contributor.authorAzizi, G
dc.contributor.authorAhmadi, M
dc.contributor.authorAbolhassani, H
dc.contributor.authorYazdani, R
dc.contributor.authorMohammadi, H
dc.contributor.authorMirshafiey, A
dc.contributor.authorRezaei, N
dc.contributor.authorAghamohammadi, A
dc.date.accessioned2018-08-26T07:40:53Z
dc.date.available2018-08-26T07:40:53Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47290
dc.description.abstractPrimary antibody deficiencies (PADs) are the most common inherited primary immunodeficiencies in humans, characterized by hypogammaglobulinemia, an inability to produce specific antibodies, and recurrent infections mainly caused by encapsulated bacteria. However, it has been shown that inflammatory disorders, granulomatous lesions, lymphoproliferative diseases, cancer, and autoimnnunity are associated with the various types of PAD. Both systemic and organ-specific autoimmune diseases could be attributed to B-cell defects in PAD patients. Immune thrombocytopenic purpura and autoimmune hemolytic anemia are the most common autoimmune disorders in this group of patients. The aim of this review is to describe the proposed mechanisms for autoimmunity and to review the literature with respect to the reported autoimmune disorders in each type of PAD. (C) 2016 S. Karger AG, Basel
dc.language.isoEnglish
dc.relation.ispartofINTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
dc.subjectPrimary antibody deficiencies
dc.subjectAutoimmunity
dc.subjectAntibody
dc.subjectAutoimmune hemolytic anemia
dc.subjectImmune thrombocytopenic purpura
dc.titleAutoimnriunity in Primary Antibody Deficiencies
dc.typeReview
dc.citation.volume171
dc.citation.issue3-4
dc.citation.spage180
dc.citation.epage193
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1159/000453263


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