Yunis E J, Good R A, Smith J, Stutman O
Proc Natl Acad Sci U S A. 1974 Jun;71(6):2544-8. doi: 10.1073/pnas.71.6.2544.
Long-lived, immunologically vigorous (C3H(f) x A(f))F(1) hybrids were produced after lethal irradiation by administration of spleen cells from C3H(f) or syngeneic donors. Further, neonatally thymectomized C3H(f) or A(f) strain donors reconstituted irradiated C3H(f) or (C3H(f) x A(f))F(1) hosts. In addition, C3H(f) spleen cells from nonthymectomized 10- to 15-day-old donors protected irradiated hybrid mice, but A(f) cells of young mice as well as of older mice produced graft-versus-host reaction and early death in irradiated C3H(f) or (C3H(f) x A(f))F(1) hybrids. Abrogation of secondary disease by treatment of irradiated mice with spleen cells from allogeneic neonatally thymectomized mice is possibly attributable to diminished immunologic competence of the cells grafted, followed by the development of immunological tolerance of the donor cells. Donor cells, receiving thymus influence in the recipient host after transplantation, could explain the long-lived immunologically vigorous radiation chimeras that did not experience graft-versus-host reactions. The findings of this study help to understand the differential susceptibility of A(f) and C3H(f) mice to development of tolerance to one another's antigens observed in prior investigations. It appears that, in these mice, the host thymus influences the maturation of the spleen cells from young mice or from neonatally thymectomized mice. However, this influence was often greater in mice given 767 rads than in those given 1046 rads. This differential influence is possibly attributable to irradiation damage to the thymus produced by the higher dose of irradiation. Spleen cells from neonatally thymectomized mice can be differentiated and expanded by the thymus of the host. The differential susceptibility of T(1), early differentiation stages, of thymus-dependent lymphocytes and T(2), late differentiation stages, of thymus-dependent lymphocytes to tolerance induction and immunostimulation, respectively, are proposed as the bases for these otherwise paradoxical influences.
通过给予来自C3H(f)或同基因供体的脾细胞进行致死性照射后,产生了寿命长、免疫活力强的(C3H(f)×A(f))F1杂种。此外,新生期切除胸腺的C3H(f)或A(f)品系供体对受照射的C3H(f)或(C3H(f)×A(f))F1宿主进行了重建。另外,来自未切除胸腺的10至15日龄供体的C3H(f)脾细胞保护了受照射的杂种小鼠,但幼龄和老龄小鼠的A(f)细胞在受照射的C3H(f)或(C3H(f)×A(f))F1杂种中产生了移植物抗宿主反应并导致早期死亡。用新生期切除胸腺的同种异体小鼠的脾细胞治疗受照射小鼠,从而消除继发性疾病,这可能归因于移植细胞免疫能力的降低,随后供体细胞产生了免疫耐受。移植后在受体宿主体内受到胸腺影响的供体细胞,可以解释未发生移植物抗宿主反应的寿命长、免疫活力强的辐射嵌合体。本研究结果有助于理解在先前研究中观察到的A(f)和C3H(f)小鼠对彼此抗原产生耐受性的不同易感性。似乎在这些小鼠中,宿主胸腺影响幼龄小鼠或新生期切除胸腺的小鼠的脾细胞成熟。然而,给予767拉德照射的小鼠中这种影响通常比给予1046拉德照射的小鼠中更大。这种差异影响可能归因于较高剂量照射对胸腺产生的辐射损伤。新生期切除胸腺的小鼠的脾细胞可由宿主的胸腺进行分化和扩增。胸腺依赖性淋巴细胞的早期分化阶段T(1)和晚期分化阶段T(2)对耐受诱导和免疫刺激的不同易感性,被认为是这些看似矛盾的影响的基础。