Sano Y, Osawa H, Sotozono C, Kinoshita S
Department of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto City, Japan.
Invest Ophthalmol Vis Sci. 1998 Sep;39(10):1953-7.
The acquisition of cell-mediated immunity against donor antigens has been shown to be associated with rejection of orthotopic corneal allografts, but the mechanisms that cause corneal allograft destruction in grafted tissue remain obscure. To determine which T-cell subsets infiltrate graft tissue and cause graft rejection, cytokine expression was examined in corneal tissue after orthotopic corneal allograft.
BALB/c mice received orthotopic corneal allografts from either syngeneic BALB/c or allogeneic C57BL/6 donors. At 1 or 4 weeks after grafting, the mice were euthanatized, and their corneas were removed. Corneal tissue was frozen, homogenized, and placed in phosphate-buffered saline (PBS). Each sample consisted of five corneas in 500 ml PBS. After centrifugation, the supernatant was collected, and the concentration of the following cytokines was measured by enzyme-linked immunosorbent assay: interleukin (IL)-1alpha, IL-2, IL-4, IL-10, interferon (IFN)-gamma, and tumor necrosis factor (TNF)-alpha.
Significantly increased amounts of proinflammatory cytokines (IL-1alpha and TNF-alpha) were detected in supernatants from all grafted corneas (both syngeneic and allogeneic) at 1 week after grafting. At 4 weeks after grafting, supernatants from normal corneas, corneas with syngeneic grafts, and corneas with accepted corneal allografts contained undetectable amounts of IL-2 and IFN-gamma, whereas supernatants from corneas with rejected corneal allografts contained significant amounts of IL-2 and IFN-gamma. There were no significant differences in the amounts of IL-4 or IL-10 among all samples. Histologic examination confirmed the expression of IL-2 and IFN-gamma in rejected corneal allografts.
Because IL-2 and IFN-gamma are secreted primarily by T-helper type 1 (Th 1) cells, whereas IL-4 and IL-10 are secreted by T-helper type 2 (Th 2) cells, these results indicate that Th 1-type cytokines, rather than Th 2-type cytokines, contribute to the rejection of orthotopic corneal allografts in graft tissue.
细胞介导的针对供体抗原的免疫已被证明与原位角膜同种异体移植排斥反应相关,但导致移植组织中角膜同种异体移植破坏的机制仍不清楚。为了确定哪些T细胞亚群浸润移植组织并导致移植排斥反应,在原位角膜同种异体移植后检测角膜组织中的细胞因子表达。
BALB/c小鼠接受来自同基因BALB/c或异基因C57BL/6供体的原位角膜同种异体移植。移植后1周或4周,对小鼠实施安乐死并取出其角膜。将角膜组织冷冻、匀浆并置于磷酸盐缓冲盐水(PBS)中。每个样本由500ml PBS中的5个角膜组成。离心后,收集上清液,并通过酶联免疫吸附测定法测量以下细胞因子的浓度:白细胞介素(IL)-1α、IL-2、IL-4、IL-10、干扰素(IFN)-γ和肿瘤坏死因子(TNF)-α。
移植后1周,在所有移植角膜(同基因和异基因)的上清液中均检测到促炎细胞因子(IL-1α和TNF-α)的量显著增加。移植后4周,正常角膜、同基因移植角膜和已接受角膜同种异体移植的角膜的上清液中IL-2和IFN-γ的量不可检测,而排斥性角膜同种异体移植角膜的上清液中含有大量的IL-2和IFN-γ。所有样本中IL-4或IL-10的量没有显著差异。组织学检查证实了IL-2和IFN-γ在排斥性角膜同种异体移植中的表达。
由于IL-2和IFN-γ主要由1型辅助性T(Th1)细胞分泌,而IL-4和IL-10由2型辅助性T(Th2)细胞分泌,这些结果表明Th1型细胞因子而非Th2型细胞因子促成了移植组织中原位角膜同种异体移植的排斥反应。