Scientific Article
previous document  unige:11464  next document
add to browser collection

The Yaa gene abrogates the major histocompatibility complex association of murine lupus in (NZB x BXSB)F1 hybrid mice

Merino, Ramon
Iwamoto, Masahiro
Gershwin, M. E.
Published in Journal of Clinical Investigation. 1994, vol. 94, no. 2, p. 521-525
Abstract To investigate the specific contribution of select MHC class II genes on the development of murine lupus, H-2 congenic (NZB x BXSB)F1 hybrid mice bearing either H-2b/b, H-2d/b, or H-2d/d haplotypes were generated. We compared the clinical development (autoantibody production and glomerulonephritis) of systemic lupus erythematosus (SLE) in these three F1 hybrids in the presence or absence of the mutant gene, Yaa (Y chromosome-linked autoimmune acceleration), which normally accelerates the progression of murine SLE. (NZB x BXSB)F1 hybrid female mice bearing either the H-2b/b or H-2d/b haplotype developed a rapid course of severe SLE, while the appearance of disease was markedly delayed in H-2d/d hybrid females. However, in the presence of the Yaa gene, H-2d/d F1 males developed SLE as severe as H-2b/b and H-2d/b F1 males. These data indicate that (a) the conventional H-2b is a haplotype leading to susceptibility for murine SLE, while H-2d is a relatively resistant haplotype; (b) the H-2b haplotype exhibits a dominant effect on autoimmune responses, similar to the classical MHC-linked Ir gene effect; and (c) most strikingly, the Yaa gene totally abrogates the MHC effect on murine lupus in (NZB x BXSB)F1 hybrid mice.
Keywords AnimalsAutoimmunity/ geneticsBase SequenceFemaleGenes, MHC Class IIH-2 Antigens/ geneticsHybridization, GeneticLinkage (Genetics)Lupus Erythematosus, Systemic/ geneticsMaleMiceMice, Inbred NZBMolecular Sequence DataMutationY Chromosome
Stable URL
Full text
PMID: 8040305
137 hits and 0 download since 2010-08-27
Export document
Format :
Citation style :