The frequency of complement receptor type 1 (CR1) gene polymorphisms in nine families with multiple cases of systemic lupus erythematosus

Arthritis Rheum. 1989 Nov;32(11):1465-9. doi: 10.1002/anr.1780321117.

Abstract

Low levels of complement receptor type 1 (CR1) on the erythrocytes of patients with systemic lupus erythematosus (SLE) may be acquired or genetically determined. Nine families with multiple cases of SLE were studied using a CR1 probe and restriction fragment length polymorphism analysis, to address this question. The absence of a significant increase in the frequency of a 6.9-kb band (previously shown to be associated with low-level CR1 on erythrocytes) suggests that this genetic marker does not play a major role in determining SLE, either in these families or in SLE patients in general.

Publication types

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

MeSH terms

  • DNA Probes
  • Erythrocytes / immunology*
  • Genetic Markers
  • Humans
  • Lupus Erythematosus, Systemic / genetics*
  • Lupus Erythematosus, Systemic / immunology
  • Nucleic Acid Hybridization
  • Pedigree
  • Polymorphism, Restriction Fragment Length*
  • Receptors, Complement / genetics*

Substances

  • DNA Probes
  • Genetic Markers
  • Receptors, Complement