Bradley S M, Morrissey P J, Sharrow S O, Singer A
J Exp Med. 1982 Jun 1;155(6):1638-52. doi: 10.1084/jem.155.6.1638.
The present study has assessed whether precursor T cells express receptors specific for the recognition of allogeneic I region-encoded determinants before their entry into the thymus. Because the ability of thymocytes to proliferate in response to allogeneic stimulator cells was shown to primarily result from the recognition of allogeneic I region determinants, thymocytes must already express anti-Ia receptors. In contrast, the expression of anti- Ia receptors by functionally immature thymocyte precursors could not be directly assessed by mixed lymphocyte reaction reactivity. However, expression of anti-Ia receptors by thymocyte precursors could be assessed by their ability to be specifically tolerized by the allogeneic Ia determinants that they encountered during their differentiation. To determine whether T cell precursors could specifically recognize and be tolerized to allogeneic Ia determinants expressed prethymically, thymus- engrafted radiation bone marrow chimeras were constructed [A {arrow} A x B (Tx + A Thy)] such that strain A T cells would be differentiating within a syngeneic strain A thymus but would have been previously exposed to the allogeneic strain B Ia determinants of the irradiated A x B host. The strain A thymocytes from these experimental animals were indeed tolerant to the extrathymic allogeneic strain B Ia determinants expressed by the irradiated host. Such tolerance was not mediated by detectable suppression and was not explained by the presence intrathymically of extrathymic allogeneic Ia determinants. Thus, these results suggest that T cell precursors can be specifically tolerized entry into the thymus. In addition, the failure to detect the generation of thymocytes with specificity for the allogeneic Ia determinants of the irradiated host, which were not deleted prethymically, argues that novel anti-allo Ia receptor specificities are not generated intrathymically.
本研究评估了前体T细胞在进入胸腺之前是否表达特异性识别同种异体I区编码决定簇的受体。由于胸腺细胞对同种异体刺激细胞增殖的能力主要源于对同种异体I区决定簇的识别,胸腺细胞必定已经表达抗Ia受体。相比之下,功能不成熟的胸腺细胞前体对抗Ia受体的表达无法通过混合淋巴细胞反应活性直接评估。然而,胸腺细胞前体对抗Ia受体的表达可通过它们在分化过程中遇到的同种异体Ia决定簇使其特异性耐受的能力来评估。为了确定T细胞前体是否能特异性识别并耐受胸腺前表达的同种异体Ia决定簇,构建了胸腺移植的辐射骨髓嵌合体[A→A×B(Tx+A Thy)],使得A系T细胞在同基因A系胸腺内分化,但此前已接触过受照射A×B宿主的同种异体B系Ia决定簇。这些实验动物的A系胸腺细胞确实耐受受照射宿主表达的胸腺外同种异体B系Ia决定簇。这种耐受不是由可检测到的抑制介导的,也不能用胸腺内存在胸腺外同种异体Ia决定簇来解释。因此,这些结果表明T细胞前体在进入胸腺时可被特异性耐受。此外,未能检测到对受照射宿主的同种异体Ia决定簇具有特异性的胸腺细胞的产生(这些决定簇在胸腺前未被清除),这表明胸腺内不会产生新的抗同种异体Ia受体特异性。