Zepp F, Cussler K, Mannhardt W, Schofer O, Schulte-Wissermann H
Department of Pediatrics, University of Mainz, FRG.
Scand J Immunol. 1987 Dec;26(6):589-601. doi: 10.1111/j.1365-3083.1987.tb02294.x.
Two new experimental approaches were established to analyse the influence of the thymus on tolerance induction to major histocompatibility complex (MHC) antigens: The aim of the first experiment was to perform successful transplantation of adult allogeneic thymus tissue into nude mice, an attempt that has been unsuccessful in the past. Tolerance for the MHC genotype of a prospective thymus graft recipient (A) was induced in mice of strain B by injection of (A X B) splenocytes during the neonatal period. Adult thymic tissue obtained from these allogeneic donors (B) were grafted into the nude mice of strain A. The allogeneic thymus was accepted by the nude mice and immunoreconstitution was achieved. Subsequently the recipients developed tolerance to the MHC antigens of the allogeneic thymus donor as proved by mixed lymphocyte cultures and the acceptance of skin grafts. The second experiment was designed to determine which Ia-positive thymic compartment participates in conferring tolerance to MHC antigens in maturing T lymphocytes. Chimaeric thymus grafts were created by transplantation of neonatal thymus (A) into allogeneic nude mice (B) for a period of 8 weeks. The graft was populated with host bone marrow-derived Ia antigen-positive cells. The chimaeric thymuses consisting of type A epithelium but populated with both type A and B lymphocytes and non-lymphoid cells (i.e. Ia-positive macrophages and dendritic cells), were newly transplanted into nude mice of strain A. The engraftment lead to immunological reconstitution and the nude mice acquired tolerance to the MHC antigens expressed by the allogeneic Ia-positive cells populating the chimaeric graft. Irradiation of the chimaeric thymus prior to transplantation allowed transplantation of chimaeric thymus devoid of living thymocytes but still populated with functionally intact Ia-positive non-lymphoid cells. Transplantation of irradiated chimaeric thymuses resulted in immunoreconstitution and induced exactly the same allotolerance pattern as described above. The results demonstrate that not thymus epithelial cells but a bone-marrow-derived non-lymphoid thymus cell, most likely the Ia-antigen-positive thymic macrophage of dendritic cell, is responsible for the induction of tolerance to MHC antigens in developing T lymphocytes.
建立了两种新的实验方法来分析胸腺对主要组织相容性复合体(MHC)抗原耐受诱导的影响:第一个实验的目的是将成年同种异体胸腺组织成功移植到裸鼠体内,这一尝试过去并不成功。通过在新生期注射(A×B)脾细胞,在B品系小鼠中诱导对预期胸腺移植受体(A)的MHC基因型的耐受。从这些同种异体供体(B)获得的成年胸腺组织被移植到A品系的裸鼠体内。裸鼠接受了同种异体胸腺,实现了免疫重建。随后,通过混合淋巴细胞培养和皮肤移植的接受证明,受体对同种异体胸腺供体的MHC抗原产生了耐受。第二个实验旨在确定哪个Ia阳性胸腺区室参与在成熟T淋巴细胞中赋予对MHC抗原的耐受。通过将新生胸腺(A)移植到同种异体裸鼠(B)中8周来创建嵌合胸腺移植。移植的胸腺中含有宿主骨髓来源的Ia抗原阳性细胞。由A型上皮组成但含有A型和B型淋巴细胞以及非淋巴细胞(即Ia阳性巨噬细胞和树突状细胞)的嵌合胸腺,被重新移植到A品系的裸鼠体内。移植导致免疫重建,裸鼠对嵌合移植中同种异体Ia阳性细胞表达的MHC抗原产生耐受。在移植前对嵌合胸腺进行照射,可以移植不含活胸腺细胞但仍含有功能完整的Ia阳性非淋巴细胞的嵌合胸腺。照射后的嵌合胸腺移植导致免疫重建,并诱导出与上述完全相同的同种耐受模式。结果表明,不是胸腺上皮细胞,而是骨髓来源的非淋巴细胞胸腺细胞,很可能是Ia抗原阳性的胸腺巨噬细胞或树突状细胞,负责在发育中的T淋巴细胞中诱导对MHC抗原的耐受。