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Further serological and RFLP analysis of the MRL-+/+ and MRL-lpr/lpr mice.

作者信息

Delarbre C, Bobe P, Kiger N, Kourilsky P, Gachelin G

机构信息

Unité de Biologie Moléculaire du Gène, INSERM U. 277, CNRS U.A.C. 115, Institut Pasteur, Paris, France.

出版信息

J Immunogenet. 1988 Oct-Dec;15(5-6):307-19. doi: 10.1111/j.1744-313x.1988.tb00434.x.

DOI:10.1111/j.1744-313x.1988.tb00434.x
PMID:2475545
Abstract

During their ageing, MRL-lpr/lpr mice (H-2k) suffer from progressive lymph node enlargement, associated with the development of several acute autoimmune lesions. The primary effect and location of the lpr mutation is unknown. However, a minority of the lymphoid cells of some MRL-+/+, as well as MRL-lpr/lpr mice, express 'alien' H-2d antigenic specificities. In the course of the investigation of the origin of the latter, we have carried out the genotyping of the MHC of several MRL-+/+ and MRL-lpr/lpr mice using the Southern blotting technique and employing a variety of MHC class I and class II probes, and restriction enzymes known to discriminate between the d and the k haplotypes. None of the results obtained so far suggests the contribution of genuine H-2d genes to the MHC of the MRL-+/+ and MRL-lpr/lpr mouse strains. Alternative hypotheses for the generation of the 'alien' epitopes are discussed.

摘要

相似文献

1
Further serological and RFLP analysis of the MRL-+/+ and MRL-lpr/lpr mice.
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Comparison of wasting syndrome in [MRL lpr/lpr-->MRL +/+] chimera and graft versus host disease in [B10.D2-->BALB/c] chimera and an attempt to transfer the wasting syndrome in [MRL lpr/lpr-->MRL +/+] to MRL +/+ mice.[MRL lpr/lpr→MRL +/+]嵌合体中消瘦综合征与[B10.D2→BALB/c]嵌合体中移植物抗宿主病的比较以及将[MRL lpr/lpr→MRL +/+]中的消瘦综合征转移至MRL +/+小鼠的尝试。
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