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. Author manuscript; available in PMC: 2015 Feb 15.
Published in final edited form as: J Immunol. 2014 Jan 17;192(4):1762–1767. doi: 10.4049/jimmunol.1302957

Figure 3.

Figure 3

Recurrent HSK in B6-CXCR2 KO mice was significantly less than in wild-type B6 mice. Eyes of mice were infected with 106 pfu of HSV-1, McKrae strain. Six weeks following infection mice were irradiated with UV-B to reactivate the latent infection. B6-CXCR2 KO mice (n=19) were compared with wild-type B6 mice (n=18) for corneal opacity (A) and corneal neovascularization (B). CXCR2 mice demonstrated significantly reduced corneal opacity and neovascularization than did wild-type B6 mice from day 7 until day 35 (P<0.01-0.001).