Stutman O, Yunis E J, Good R A
J Exp Med. 1972 Feb 1;135(2):339-56. doi: 10.1084/jem.135.2.339.
The immune functions of neonatally thymectomized C3Hf mice exposed only temporarily to thymus function show a progressive decay with time in the absence of the thymus. The immune responses studied at different ages in the range of 100-600 days were: first-set rejection of H-2-compatible and incompatible skin allografts, second-set rejection of skin allografts, capacity of spleen cells to produce graft-versus-host reactions in F(1) hybrids, resistance to infection with mouse hepatitis virus, and response of spleen cells to phytohemagglutinin in vitro. These long-term studies had the purpose of determining the duration of the restoration induced by thymus function when the mice were exposed only temporarily to it. Different models were used but the two basic ones were: (a) mice grafted intraperitoneally at 15 days of age with a syngeneic thymus that was removed surgically at 10, 20, or 30 days after grafting, and (b) mice grafted at 15 days of age with allogeneic strain A thymoma or C57BL thymus, these representing situations in which there is spontaneous rejection of the restoring graft. In all the experimental models used, the animals were restored when tested at 100 days of age, but progressively became immunologically incapacitated at 200-300 days of age. From the more controlled experiments in which the restoring thymus graft was removed surgically, the following conclusions can be drawn. (a) A short exposure to a thymus graft can produce restoration of immune functions in neonatally thymectomized mice, but this restoration is not self-sustaining in the absence of the thymus and declines progressively with age. The decline usually starts at 200-300 days of age. (b) This was especially clear in experiments in which the same animal was tested twice in its lifetime for capacity to produce graft-versus-host reactions; these animals were competent at 100 days and became incompetent at 400 days of age. (c) The shortest period of thymic exposure studied was 10 days; if vascularization of the graft is taken into account, 2-3 days of thymic function are sufficient to produce restoration. (d) The immune decay observed in the thymectomized animals exposed temporarily to thymus was more profound than the physiological decay of immunity observed in control animals of similar age. (e) Of all the tests studied, the response of spleen cells to phytohemagglutinin was to be preserved the longest in animals exposed only temporarily to thymic function. The present results were interpreted in accordance with our previous findings indicating that a population of postthymic cells can be developed by temporary exposure of neonatally thymectomized animals to thymic function, but that this population is not self-sustaining in the absence of thymus and progressively decays by physiological attrition.
仅短暂接触胸腺功能的新生期切除胸腺的C3Hf小鼠,在无胸腺的情况下,其免疫功能会随着时间逐渐衰退。在100 - 600天龄范围内不同年龄段所研究的免疫反应包括:对H - 2相容和不相容皮肤同种异体移植物的初次排斥反应、皮肤同种异体移植物的二次排斥反应、脾细胞在F(1)杂种中产生移植物抗宿主反应的能力、对小鼠肝炎病毒感染的抵抗力以及脾细胞在体外对植物血凝素的反应。这些长期研究的目的是确定当小鼠仅短暂接触胸腺功能时,胸腺功能诱导的恢复持续时间。使用了不同的模型,但两个基本模型是:(a) 15日龄时腹腔内移植同基因胸腺的小鼠,在移植后10、20或30天手术切除该胸腺;(b) 15日龄时移植同种异体A品系胸腺瘤或C57BL胸腺的小鼠,这些代表恢复性移植物会被自发排斥的情况。在所有使用的实验模型中,动物在100日龄时接受测试时免疫功能得到恢复,但在200 - 300日龄时逐渐丧失免疫能力。从更具可控性的手术切除恢复性胸腺移植物的实验中,可以得出以下结论。(a) 短暂接触胸腺移植物可使新生期切除胸腺的小鼠免疫功能恢复,但在无胸腺的情况下这种恢复不能自我维持,且会随着年龄增长逐渐衰退。衰退通常在200 - 300日龄开始。(b) 在同一动物一生中两次测试其产生移植物抗宿主反应能力的实验中,这一点尤为明显;这些动物在100日龄时有能力,而在400日龄时变得无能力。(c) 所研究的最短胸腺接触期为10天;如果考虑移植物的血管化,2 - 3天的胸腺功能足以产生恢复。(d) 在短暂接触胸腺的切除胸腺动物中观察到的免疫衰退比同龄对照动物中观察到的生理性免疫衰退更为严重。(e) 在所有研究的测试中,仅短暂接触胸腺功能的动物中,脾细胞对植物血凝素的反应保留时间最长。根据我们之前的研究结果对目前的结果进行了解释,表明新生期切除胸腺的动物短暂接触胸腺功能可发育出一群胸腺后细胞,但该群体在无胸腺的情况下不能自我维持,并会因生理性损耗而逐渐衰退。