Mercadal C M, Bouley D M, DeStephano D, Rouse B T
Department of Microbiology and Veterinary Medicine, University of Tennessee, Knoxville 37996-0845.
J Virol. 1993 Jun;67(6):3404-8. doi: 10.1128/JVI.67.6.3404-3408.1993.
Infections of the cornea with herpes simplex virus type 1 cause inflammatory lesions which frequently lead to blindness. The disease is suspected to be immunopathological in nature. To establish this point and to study possible mechanisms involved, corneal infections in C.B-17 scid/scid and cell-reconstituted scid mice were investigated. Whereas unreconstituted scid mice failed to develop herpetic stromal keratitis (HSK) and died of encephalitis, mice reconstituted with T lymphocytes generated severe lesions. T cells of the CD4+ subset were found to be essential mediators of the HSK lesion, while T cells of the CD8+ subset protected mice from lethality. The results confirm that HSK is an immunopathological disease and that scid mice provide a convenient model that should prove valuable in establishing the biochemical mechanisms by which HSK is mediated.
1型单纯疱疹病毒引起的角膜感染会导致炎症性病变,常常导致失明。这种疾病被怀疑本质上是免疫病理性的。为了证实这一点并研究其中可能涉及的机制,对C.B-17 scid/scid小鼠和细胞重建的scid小鼠的角膜感染进行了研究。未重建的scid小鼠未能发生疱疹性基质性角膜炎(HSK)并死于脑炎,而用T淋巴细胞重建的小鼠则产生了严重病变。发现CD4+亚群的T细胞是HSK病变的关键介质,而CD8+亚群的T细胞则保护小鼠免于死亡。结果证实HSK是一种免疫病理性疾病,并且scid小鼠提供了一个便利的模型,在确立介导HSK的生化机制方面应会证明是有价值的。