Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

J Clin Invest. 1987 May;79(5):1395-400. doi: 10.1172/JCI112967.

Abstract

The X-linked form of severe combined immunodeficiency (XSCID) is underdiagnosed because no methods have been available for detecting carriers. Although boys with XSCID are deficient in T cells, female carriers are immunologically normal. Carriers' normal immune function would be expected if all their T cells were derived from precursors whose X chromosome bearing the XSCID mutation was inactivated early in embryogenesis. Using somatic cell hybridization to separate the active and inactive X chromosomes and restriction fragment length polymorphisms to distinguish them, we have determined the lymphocyte X inactivation pattern in XSCID carriers and their female relatives. In the T cells of three carriers, the X chromosome bearing the XSCID mutation was consistently inactive. Nonrandom X inactivation was also found in the T cells of one at-risk female, while two others had normal, random X inactivation. This method constitutes a generally applicable carrier test for XSCID.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Dosage Compensation, Genetic*
  • Female
  • Genetic Carrier Screening / methods*
  • Humans
  • Immunologic Deficiency Syndromes / genetics*
  • Mathematics
  • Mutation
  • Pedigree
  • Polymorphism, Restriction Fragment Length