Zinkernagel R M
Thymus. 1981 Apr;2(6):321-7.
Adult-thymectomised lethally mice A that were reconstituted with T-cell-depleted bone marrow cells of (A X B)F1 origin plus fetal thymus grafts of (B X C)F1 origin generated virus-specific T cells restricted to B alone; adult-thymectomised and lethally irradiated (A X B)F1 mice that were reconstituted with T-cell-depleted bone marrow cells of (A X B)F1 origin plus fetal thymus grafts of A and of B origin generated virus-specific T cells restricted to A or to B. These results do not reveal obvious suppressive influences of host or stem-cell origin that might have explained results obtained with various irradiated bone marrow or thymus chimeras, they indicate that the thymus' influence on maturing T cells is one of the limiting steps in the selection of T cells' restriction specificities.
用(A×B)F1来源的T细胞耗竭骨髓细胞加(B×C)F1来源的胎儿胸腺移植重建的成年去胸腺致死性A小鼠产生仅受B限制的病毒特异性T细胞;用(A×B)F1来源的T细胞耗竭骨髓细胞加A和B来源的胎儿胸腺移植重建的成年去胸腺并接受致死性照射的(A×B)F1小鼠产生受A或B限制的病毒特异性T细胞。这些结果并未揭示宿主或干细胞来源可能解释各种照射骨髓或胸腺嵌合体所获结果的明显抑制作用,它们表明胸腺对成熟T细胞的影响是T细胞限制性特异性选择中的限制步骤之一。