Aldrich C J, Ljunggren H G, Van Kaer L, Ashton-Rickardt P G, Tonegawa S, Forman J
Department of Microbiology, University of Texas Southwestern Medical Center at Dallas 75235-9048.
Proc Natl Acad Sci U S A. 1994 Jul 5;91(14):6525-8. doi: 10.1073/pnas.91.14.6525.
Mice with a homozygous deletion in their Tap-1 gene (-/- mice) express very low levels of cell membrane major histocompatibility complex class I molecules and have < 1% peripheral CD8+ T cells. We show that these -/- mice but not their +/- littermates display strong primary syngeneic anti-H-2Kb and -Db-specific responses mediated by CD8+ T cells. These responses are augmented by in vivo priming. Further, -/- mice primed in vivo with H-2d alloantigens generate an anti-H-2d response which appears nearly as strong as that found in +/- littermates. Both -/- anti-H-2b and anti-H-2d T cells do not recognize target cells from Tap-1 -/- animals or Tap-2-deficient RMA-S cells. Thus, some CD8+ anti-self and alloreactive T cells can be selected in the absence of Tap proteins.
在其Tap-1基因中存在纯合缺失的小鼠(-/-小鼠)表达极低水平的细胞膜主要组织相容性复合体I类分子,并且外周CD8+ T细胞少于1%。我们发现,这些-/-小鼠而非其+/-同窝小鼠表现出由CD8+ T细胞介导的强烈的原发性同基因抗H-2Kb和-Db特异性反应。这些反应通过体内致敏而增强。此外,用H-2d同种异体抗原在体内致敏的-/-小鼠产生的抗H-2d反应几乎与+/-同窝小鼠中发现的反应一样强烈。-/-抗H-2b和抗H-2d T细胞均不识别来自Tap-1 -/-动物或Tap-2缺陷型RMA-S细胞的靶细胞。因此,在没有Tap蛋白的情况下可以选择一些CD8+抗自身和同种反应性T细胞。