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• W2091567372 endingPage "1922" @default.
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• W2091567372 abstract "We have proposed that significant subsets of individuals with IgA deficiency (IgA-D) and common variable immunodeficiency (CVID) may represent polar ends of a clinical spectrum reflecting a single underlying genetic defect. This proposal was supported by our finding that individuals with these immunodeficiencies have in common a high incidence of C4A gene deletions and C2 rare gene alleles. Here we present our analysis of the MHC haplotypes of 12 IgA-D and 19 CVID individuals from 21 families and of 79 of their immediate relatives. MHC haplotypes were defined by analyzing polymorphic markers for 11 genes or their products between the HLA-DQB1 and the HLA-A genes. Five of the families investigated contained more than one immunodeficient individual and all of these included both IgA-D and CVID members. Analysis of the data indicated that a small number of MHC haplotypes were shared by the majority of immunodeficient individuals. At least one of two of these haplotypes was present in 24 of the 31 (77%) immunodeficient individuals. No differences in the distribution of these haplotypes were observed between IgA-D and CVID individuals. Detailed analysis of these haplotypes suggests that a susceptibility gene or genes for both immunodeficiencies are located within the class III region of the MHC, possibly between the C4B and C2 genes." @default.
• W2091567372 created "2016-06-24" @default.
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• W2091567372 date "1992-06-01" @default.
• W2091567372 modified "2023-10-14" @default.
• W2091567372 title "Major histocompatibility complex class III genes and susceptibility to immunoglobulin A deficiency and common variable immunodeficiency." @default.
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• W2091567372 doi "https://doi.org/10.1172/jci115797" @default.
• W2091567372 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/295891" @default.
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