| Literature DB >> 6778930 |
E van Loghem, R I Sukernik, L P Osipova, B J Zegers, H Matsumoto, G de Lange, G Lefranc.
Abstract
Individuals with selective absence of IgG1 and IgG2 were discovered by testing for allotypes and isotypes of the respective sub-classes. These individuals were homozygous for sub-class deleted Gm-Am haplotypes, as shown by allotype studies in two families (Gm--;..;g;A2m1/Gm--;n;b;A2m1 and Gm--;n;b;A2m1/Gm--;..;b;A2m1) and by a population study of New Guineans (Gm fa;--;b;A2m2). The individuals with IgG1 sub-class deficiency showed elevation of IgG2, IgG4 and in particular of IgG3. Gene deletion can result from unequal crossing over which renders a complementary chromosome with a duplication of a sub-class gene. In one family, duplication of gamma 3 genes was observed to have happened in one of a twin pair. Quanitation of sub-classes in families with gamma 1- and with gamma 3-duplicated haplotypes did not show increased levels of the gene involved.Entities:
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Year: 1980 PMID: 6778930 DOI: 10.1111/j.1744-313x.1980.tb00722.x
Source DB: PubMed Journal: J Immunogenet ISSN: 0305-1811