CD8 T Cells Mediate Transient Herpes Stromal Keratitis in CD4-Deficient Mice

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Abstract
Purpose. To evaluate the role of CD4+ T cells in the development of murine herpes stromal keratitis (HSK). methods. The corneas of wild-type (WT) BALB/c mice and three types of CD4-deficient BALB/c mice (CD4−/−, CD4-depleted, CD4 and CD8 double-depleted) were infected with different doses of HSV-1 RE, and HSK incidence and severity were monitored. Corneal infiltrates were quantitatively and functionally assayed by flow cytometric analysis of individually digested diseased corneas and documented histologically. results. At a relatively high infectious dose (1 × 105 pfu/cornea): (1) CD4-deficient and WT BALB/c mice had severe HSK with a similar incidence (80%–100%), whereas HSK did not develop in mice deficient in both CD4+ and CD8+ T cells; (2) neutrophils were the predominate leukocyte in the corneas of CD4-deficient and WT mice; (3) the corneas of WT mice had activated, HSV-1-specific CD4+ T cells, but few if any CD8+ T cells; (4) the corneas of CD4-deficient mice had activated, HSV-1-specific CD8+ T cells; and (5) HSK in CD4-deficient mice was transient, showing loss of CD8+ T cells at 2 to 3 weeks after infection (pi) followed by a loss of neutrophils. At a relatively low infectious dose of HSV-1 (103 pfu/cornea) severe HSK developed in 80% to 90% of WT mice, but in only 30% to 40% of CD4-deficient mice. conclusions. CD4+ T cells preferentially mediate HSK, but, in their absence, a high infectious dose of HSV-1 can induce histologically similar but transient HSK that is mediated by CD8+ T cells.