| Literature DB >> 3876922 |
G S Eisenbarth, S Srikanta, E Fleischnick, O P Ganda, R A Jackson, S J Brink, J S Soeldner, E J Yunis, C Alper.
Abstract
In a prospective screening program for type I diabetes mellitus, we identified a unique family in which several members (mother and three siblings) expressed an unusual set of HLA-DR alleles (DR2+, DR3/4-) and were in different phases of immunologically mediated islet beta cell dysfunction. Immunologic and/or clinical manifestations of type I diabetes were absent in all siblings not sharing both HLA haplotypes in common with the proband. This article illustrates: the clinical utility of prospective family screening for predictive markers, such as islet cell antibodies, progressive autoimmune beta cell destruction can occur in the absence of the "high-risk" alleles HLA-DR3 and DR4, and HLA identity with the proband, rather than specific HLA alleles, i.e., presence of DR3, DR4 and absence of DR2, is an essential factor.Entities:
Mesh:
Substances:
Year: 1985 PMID: 3876922 DOI: 10.2337/diacare.8.5.477
Source DB: PubMed Journal: Diabetes Care ISSN: 0149-5992 Impact factor: 19.112