Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome.

Published

Journal Article

Recent studies have shown that mutations in a newly described RNA editing enzyme, activation-induced cytidine deaminase (AID), can cause an autosomal recessive form of hyper IgM syndrome. To determine the relative frequency of mutations in AID, we evaluated a group of 27 patients with hyper IgM syndrome who did not have defects in CD40 ligand and 23 patients with common variable immunodeficiency. Three different mutations in AID were identified in 18 patients with hyper IgM syndrome, including 14 French Canadians, 2 Lumbee Indians, and a brother and sister from Okinawa. No mutations were found in the remaining 32 patients. In the group of patients with hyper IgM syndrome, the patients with mutations in AID were older at the age of diagnosis, were more likely to have positive isohemagglutinins, and were less likely to have anemia, neutropenia, or thrombocytopenia. Lymphoid hyperplasia was seen in patients with hyper IgM syndrome and normal AID as well as the patients with hyper IgM syndrome and defects in AID.

Full Text

Duke Authors

Cited Authors

  • Minegishi, Y; Lavoie, A; Cunningham-Rundles, C; Bédard, PM; Hébert, J; Côté, L; Dan, K; Sedlak, D; Buckley, RH; Fischer, A; Durandy, A; Conley, ME

Published Date

  • December 2000

Published In

Volume / Issue

  • 97 / 3

Start / End Page

  • 203 - 210

PubMed ID

  • 11112359

Pubmed Central ID

  • 11112359

International Standard Serial Number (ISSN)

  • 1521-6616

Digital Object Identifier (DOI)

  • 10.1006/clim.2000.4956

Language

  • eng

Conference Location

  • United States