Perforin pathway is essential for protection of mice against lethal ocular HSV-1 challenge but not corneal scarring

被引:26
作者
Ghiasi, H
Cai, S
Perng, GC
Nesburn, AB
Wechsler, SL
机构
[1] Cedars Sinai Burn & Allen Res Inst, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Ophthalmol, Los Angeles, CA 90024 USA
关键词
perforin; HSV-1; ocular; eye disease; protection;
D O I
10.1016/S0168-1702(99)00107-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Perforin (cytolysin; pore-forming protein) is expressed in both CD8(+) cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells, and is a major factor responsible for the cytolytic activities of these cells. Both CD8(+) T-cells and NK cells are important in eliminating cells infected with certain viruses. We examined the role of perforin in a mouse model of HSV-1 infection using perforin-deficient mice. Naive perforin knockout (perforin(o/o)) mice were more susceptible to lethal HSV-1 ocular challenge (60% survival), than naive parental C57BL/6 (100% survival). In contrast. both C57BL/6 and perforin(o/o) mice had similar levels of HSV-1 induced corneal scarring. Vaccination of perforin(o/o) mice induced a significantly higher HSV-1 neutralizing antibody titer than vaccination of C57BL/6 mice, and the mice were completely protected against lethal ocular challenge. These results suggest that in naive mice ocularly challenged with HSV-1, the perforin pathway was involved in protection against death, but not in protection against corneal scarring. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 101
页数:5
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