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Self-Reactivity and the Expression of Memory Markers Vary Independently in MRL-Mp+/+ and MRL-Mp-lpr/lpr Mice
Authors:Lesley Smyth  Michelle Howell  I Nicholas Crispe
Institution:1. ICAPB, Zoology Building, West Mains Road, Edinburgh, Scotland.;2. University of Glasgow Medical School, Glasgow, Scotland.;3. Immunobiology Section, Yale Medical School, 310 Cedar Street, New Haven, Connecticut, 06510, USA,
Abstract:MRL-Mp-lpr/lpr mice contain phenotypically abnormal populations of T cells, and exhibit an SLE-like autoimmune disease in which autoantibodies are a prominent feature. We analyzed the phenotype and T-cell receptor Vß expression pattern in CD4+ T cells of this mutant mouse strain to detect abnormalities that could explain the autoimmunity. The CD4+ T cells contain two distinct abnormal populations. One of these expresses B220 and HSA, and in these and other respects closely resembles the accumulating CD4CD8 population. The other expresses a high level of CD44 (Pgp-1), and a high level of the 16A epitope of CD45, and so resembles post-activation T cells. Both of these cell types are exclusive to MRL-Mp-lpr/lpr. We also identified V ß5- and V ß11-positive CD4+ T cells, in both MRL-Mp-lpr/lpr and MRL-Mp-+/+ mice. We conclude that autoimmune T cells can be detected in these mice, but that they are not the cause of the accumulation of abnormal CD4+ and CD4CD8cells.
Keywords:MRL  lpr  T-cell repertoire  CD4+ cell subsets
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