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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.accessioned2018-08-26T08:36:49Z
dc.date.available2018-08-26T08:36:49Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52783
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 autoimmunity 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. é 2017 S. Karger AG, Basel.
dc.language.isoEnglish
dc.relation.ispartofInternational Archives of Allergy and Immunology
dc.subjectautoimmune disease
dc.subjectautoimmunity
dc.subjectcommon variable immunodeficiency
dc.subjectdisease predisposition
dc.subjecthuman
dc.subjecthumoral immune deficiency
dc.subjecthyper IgM syndrome
dc.subjectimmunoglobulin A deficiency
dc.subjectlipopolysaccharide responsive and beige like anchor deficiency
dc.subjectprimary antibody deficiency
dc.subjectpriority journal
dc.subjectprotein deficiency
dc.subjectprotein kinase c delta deficiency
dc.subjectReview
dc.subjectX linked agammaglobulinemia
dc.subjectagammaglobulinemia
dc.subjectAutoimmune Diseases
dc.subjectblood
dc.subjectimmunological tolerance
dc.subjectimmunology
dc.subjectantibody
dc.subjectAgammaglobulinemia
dc.subjectAntibodies
dc.subjectAutoimmune Diseases
dc.subjectAutoimmunity
dc.subjectHumans
dc.subjectImmune Tolerance
dc.titleAutoimmunity in Primary Antibody Deficiencies
dc.typeArticle
dc.citation.volume171
dc.citation.issue4
dc.citation.spage180
dc.citation.epage193
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1159/000453263


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