Matossian-Rogers A, de Giorgi L
Department of Immunology, Royal London Hospital Medical College, U.K.
Immunology. 1993 Jan;78(1):122-6.
Tolerance to the minor lymphocyte stimulating (Mls) self-antigens has been shown to be due to the intrathymic deletion of T-cell clones bearing certain T-cell receptor (TcR) V beta regions. T cells bearing these V beta regions (V beta 6, V beta 7, V beta 8.1, V beta 9) are deleted in Mlsa-positive mice. This report demonstrates that hyperimmunization of AKR mice with anti-V beta 6 breaks tolerance to the self-antigen Mlsa and induces the development of anti-Mlsa antibodies. These antibodies had the capacity to block Mlsa-induced mixed lymphocyte responses between H-2 identical strain combinations and also between Mlsa-congeneic BALB.D2MA and parental BALB/c strains. Furthermore, when the responder lymphocytes were Mlsa-positive their response to allogeneic major or minor histocompatibility antigens was enhanced in the presence of this antiserum. This indicates that Mlsa may be present on T cells and that occupancy of this ligand leads to enhanced signal transduction.
对次要淋巴细胞刺激(Mls)自身抗原的耐受性已被证明是由于胸腺内带有某些T细胞受体(TcR)Vβ区域的T细胞克隆缺失所致。带有这些Vβ区域(Vβ6、Vβ7、Vβ8.1、Vβ9)的T细胞在Mlsa阳性小鼠中被删除。本报告表明,用抗Vβ6对AKR小鼠进行超免疫可打破对自身抗原Mlsa的耐受性,并诱导抗Mlsa抗体的产生。这些抗体能够阻断Mlsa诱导的H-2相同品系组合之间以及Mlsa同基因BALB.D2MA和亲本BALB/c品系之间的混合淋巴细胞反应。此外,当应答淋巴细胞为Mlsa阳性时,在这种抗血清存在的情况下,它们对同种异体主要或次要组织相容性抗原的反应会增强。这表明Mlsa可能存在于T细胞上,并且该配体被占据会导致信号转导增强。