Autoimmunity in Primary Antibody Deficiencies
dc.contributor.author | Azizi, G | |
dc.contributor.author | Ahmadi, M | |
dc.contributor.author | Abolhassani, H | |
dc.contributor.author | Yazdani, R | |
dc.contributor.author | Mohammadi, H | |
dc.contributor.author | Mirshafiey, A | |
dc.contributor.author | Rezaei, N | |
dc.contributor.author | Aghamohammadi, A | |
dc.date.accessioned | 2018-08-26T08:36:49Z | |
dc.date.available | 2018-08-26T08:36:49Z | |
dc.date.issued | 2017 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52783 | |
dc.description.abstract | Primary 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.iso | English | |
dc.relation.ispartof | International Archives of Allergy and Immunology | |
dc.subject | autoimmune disease | |
dc.subject | autoimmunity | |
dc.subject | common variable immunodeficiency | |
dc.subject | disease predisposition | |
dc.subject | human | |
dc.subject | humoral immune deficiency | |
dc.subject | hyper IgM syndrome | |
dc.subject | immunoglobulin A deficiency | |
dc.subject | lipopolysaccharide responsive and beige like anchor deficiency | |
dc.subject | primary antibody deficiency | |
dc.subject | priority journal | |
dc.subject | protein deficiency | |
dc.subject | protein kinase c delta deficiency | |
dc.subject | Review | |
dc.subject | X linked agammaglobulinemia | |
dc.subject | agammaglobulinemia | |
dc.subject | Autoimmune Diseases | |
dc.subject | blood | |
dc.subject | immunological tolerance | |
dc.subject | immunology | |
dc.subject | antibody | |
dc.subject | Agammaglobulinemia | |
dc.subject | Antibodies | |
dc.subject | Autoimmune Diseases | |
dc.subject | Autoimmunity | |
dc.subject | Humans | |
dc.subject | Immune Tolerance | |
dc.title | Autoimmunity in Primary Antibody Deficiencies | |
dc.type | Article | |
dc.citation.volume | 171 | |
dc.citation.issue | 4 | |
dc.citation.spage | 180 | |
dc.citation.epage | 193 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.1159/000453263 |
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