Exact Ground States in Spin Systems with Orbital Degeneracy

We present exact ground states in spin models with orbital generacy in one and higher dimensions. A method to obtain the exact ground states of the models when the Hamiltonians are composed of the products of two commutable operators is proposed. For the case of the spin-1/2 model with two-fold degeneracy some exact ground states are given, such as the Valence-Bond (VB), the magnetically ordered, and the orbitally ordered states under particular parameter regimes. We also find the models with the higher spin and degeneracy which have the new types of VB ground states in the spin and the orbital sectors.Comment: 4 pages(JPSJ.sty), 2 figures(EPS), to appear in J. Phys. Soc. Jpn. 68, No.2 (1999) 32

A pivotal role of cell-bound but not soluble CD4 molecules in full development of lupus-like manifestations in MRL-Faslprcg/Faslprcg mice

The role of CD4 molecules in the autoimmune and lymphoproliferative syndrome caused by murine Fas mutations was studied using the novel systemic lupus erythematosus (SLE) model, MRL-Faslprcg/Faslprcg (MRL-lprcg) mice, in combination with the novel mutant CD4 gene producing soluble CD4 (sCD4) instead of membrane-bound CD4 (mCD4). For this purpose, various autoimmune manifestations were compared among MRL-lprcg mice homozygous (CD4slprcg), heterozygous (CD4s/mlprcg), and wild-type (CD4mlprcg) for the CD4 mutation. The mortality, glomerulonephritis, proteinuria, and lymphadenopathy were significantly ameliorated in CD4slprcg compared with CD4mlprcg and CD4s/mlprcg mice, both being comparable in these clinical characteristics. In parallel with the clinical improvement, the serum levels of immunoglobulin, anti-DNA antibodies, anti-nuclear antibodies and immune complexes, and the extent of glomerular immune deposition, were significantly lower in the former. The results indicate that mCD4 is important and can not be replaced by sCD4 in full development of SLE-like manifestations, and suggest that CD4+ T cells may aggravate the autoimmune disease by stimulating autoreactive B cells to produce autoantibodies through their helper activity in Fas mutant models. The sCD4 levels in the serum and spleen elevated with the increased accumulation of B220+CD4−CD8− (double-negative (DN)) T cells in CD4slprcg mice. This, together with the significantly milder lymphadenopathy associated with lower DN T cell contents in CD4slprcg than CD4mlprcg mice, implies that some of abnormal DN T cells may be derived from cells of the CD4 lineage