Kimura T, Murata Y, Yamaguchi T, Okumura K
Nippon Ganka Gakkai Zasshi. 1989 Jan;93(1):124-31.
In herpetic keratitis, the role of T cell subsets is not clearly understood although the involvement of cell-mediated immunity has been reported. The purpose of this paper is to analyse T cell-mediated immunopathological conditions and the role of non-T cell lineage in herpetic stromal keratitis employing nude (nu/nu) and Balb/c mice. All mice were divided into three groups. Group 1: Herpes simplex virus type 1 (HSV-1)-inoculated nu/nu mice. Group 2: HSV-1-inoculated nu/nu mice with interleukin-2 (IL-2). Group 3: HSV-1-inoculated Balb/c mice. The conditions of the disease were compared in those three groups clinically and by using histological and immunopathological staining. Following antibodies were employed: anti-Asialo GMI (natural killer). anti-Thy 1 (pan-T). anti-L3T4 (helper/inducer), anti-Lyt 2 (suppressor/killer), anti-Mac 3 (macrophage), anti-Mice Immunoglobulins (monocyte. B.). Corneal lesions showed a reduced inflammatory tendency in nu/nu mice. Topical application of IL-2 in nu/nu mice induced moderate stromal inflammation compared with nu/nu mice. However, the severity of these was less than in Balb/c. Many natural killer cells (NK) were found in nu/nu mice but few in Balb/c mice. These results confirm the involvement of T-cell mediated immunity in stromal inflammation and indicate that NK cell may have an important role in suppressed T-cell immunity in nu/nu mice but are not involved in stromal inflammation.
在疱疹性角膜炎中,尽管已有报道细胞介导的免疫参与其中,但T细胞亚群的作用仍未完全明确。本文旨在利用裸鼠(nu/nu)和Balb/c小鼠分析T细胞介导的免疫病理状况以及非T细胞谱系在疱疹性基质性角膜炎中的作用。所有小鼠分为三组。第1组:接种单纯疱疹病毒1型(HSV-1)的nu/nu小鼠。第2组:接种HSV-1并注射白细胞介素-2(IL-2)的nu/nu小鼠。第3组:接种HSV-1的Balb/c小鼠。通过临床观察以及组织学和免疫病理染色对这三组小鼠的病情进行比较。使用了以下抗体:抗去唾液酸GM1(自然杀伤细胞)、抗Thy 1(全T细胞)、抗L3T4(辅助/诱导性T细胞)、抗Lyt 2(抑制/杀伤性T细胞)、抗Mac 3(巨噬细胞)、抗小鼠免疫球蛋白(单核细胞、B细胞)。角膜病变显示nu/nu小鼠的炎症倾向减轻。与未注射IL-2的nu/nu小鼠相比,局部应用IL-2可诱导nu/nu小鼠出现中度基质炎症。然而,其严重程度低于Balb/c小鼠。在nu/nu小鼠中发现了许多自然杀伤细胞(NK),而在Balb/c小鼠中则很少。这些结果证实了T细胞介导的免疫参与了基质炎症,并表明NK细胞可能在nu/nu小鼠受抑制的T细胞免疫中起重要作用,但不参与基质炎症。