EFFECT OF LONG-TERM ANTI-CD4 OR ANTI-CD8 TREATMENT ON THE DEVELOPMENTOF LPC CD4(-) CD8(-) DOUBLE-NEGATIVE T-CELLS AND OF THE AUTOIMMUNE SYNDROME IN MRL-LPR LPR MICE/

Citation
R. Merino et al., EFFECT OF LONG-TERM ANTI-CD4 OR ANTI-CD8 TREATMENT ON THE DEVELOPMENTOF LPC CD4(-) CD8(-) DOUBLE-NEGATIVE T-CELLS AND OF THE AUTOIMMUNE SYNDROME IN MRL-LPR LPR MICE/, Journal of autoimmunity, 8(1), 1995, pp. 33-45
Citations number
47
Categorie Soggetti
Immunology
Journal title
ISSN journal
08968411
Volume
8
Issue
1
Year of publication
1995
Pages
33 - 45
Database
ISI
SICI code
0896-8411(1995)8:1<33:EOLAOA>2.0.ZU;2-T
Abstract
We have determined the effect of anti-CD4 or anti-CD8 monoclonal antib ody (mAb) treatment from birth on the generation of the Epr CD4(-) CD8 (-) double-negative (DN) T cell subset and on the development of lupus -like autoimmune syndrome in MRL-lprllpr mice. Both anti-CD4 and anti- CDS mAb treatments resulted in a marked inhibition of lymphadenopathy, whereas the development of the lpr DN T cells and of the lupus-like a utoimmune syndrome strikingly differed in these two groups of mice. Th e treatment with anti-CD8 mAb almost completely blocked the appearance of the lpr DN T cells without any significant effect on the developme nt of lupus-like autoimmune syndrome in MRL-lprllpr mice. In contrast, mice treated with anti-CD4 mAb failed to develop a lupus-like syndrom e, while they still developed the lpr DN T cell subset, the predominan t population in their lymph nodes, although absolute numbers were mark edly diminished. Our results support the idea that CD8(+) T cells are a major source of the lpr DN T cells, and that the lpr DN T cells play a minor, if any, role in the pathogenesis of lupus-like autoimmune sy ndrome in MRL-lprllpr mice.