Takahashi H, Germain R N, Moss B, Berzofsky J A
Molecular Immunogenetics and Vaccine Research Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
J Exp Med. 1990 Feb 1;171(2):571-6. doi: 10.1084/jem.171.2.571.
We have observed that a peptide corresponding to an immunodominant epitope of the HIV-1 envelope protein recognized by class I MHC-restricted CD8+ CTL can also induce T cell help for itself. The help is necessary for restimulation of CTL precursors in vitro with peptide alone in the absence of exogenous lymphokines, can be removed by depletion of CD4+ T cells, and can be replaced by exogenous IL-2. Whereas the CTL in BALB/c or B10. D2 mice are restricted by the class I molecule Dd, the Th cells are restricted by the class II molecule Ad, and the help can be blocked by anti-Ad mAb. To examine the genetic regulation of the induction of help, we studied B10.A mice that share the class I Dd molecule, but have different class II molecules, Ak and Ek. Spleen cells of immune B10.A mice behave like CD4-depleted BALB/c spleen cells in that they cannot be restimulated in vitro by the peptide alone, but can with peptide plus IL-2. Therefore, in the absence of exogenous lymphokines, peptide-specific help is necessary for restimulation with this immunodominant CTL epitope peptide, and in H-2d mice, this peptide stimulates help for itself as well as CTL. We speculate on the implications of these findings for the immunodominance of this peptide in H-2d mice, and for the selective advantage of pairing certain class I and class II molecules in an MHC haplotype.
我们观察到,一种与I类MHC限制性CD8 + CTL识别的HIV-1包膜蛋白免疫显性表位相对应的肽,也能为其自身诱导T细胞辅助。在没有外源性细胞因子的情况下,这种辅助对于仅用肽在体外重新刺激CTL前体是必要的,可通过耗尽CD4 + T细胞来去除,并且可用外源性IL-2替代。在BALB/c或B10.D2小鼠中,CTL受I类分子Dd限制,而Th细胞受II类分子Ad限制,并且这种辅助可被抗Ad单克隆抗体阻断。为了研究辅助诱导的遗传调控,我们研究了共享I类Dd分子但具有不同II类分子Ak和Ek的B10.A小鼠。免疫的B10.A小鼠的脾细胞表现得像耗尽CD4的BALB/c脾细胞,即它们不能仅用肽在体外重新刺激,但可与肽加IL-2一起重新刺激。因此,在没有外源性细胞因子的情况下,肽特异性辅助对于用这种免疫显性CTL表位肽进行重新刺激是必要的,并且在H-2d小鼠中,这种肽既能刺激自身的辅助又能刺激CTL。我们推测了这些发现对于该肽在H-2d小鼠中的免疫显性以及对于在MHC单倍型中配对某些I类和II类分子的选择优势的意义。