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/
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
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.