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Department of Anatomy/Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201
Evidence suggests that Pseudomonas aeruginosa
stromal keratitis and corneal perforation (susceptibility) is a
CD4+ T cell-regulated inflammatory response following
experimental P. aeruginosa infection. This study
examined the role of Langerhans cells (LC) and the B7/CD28
costimulatory pathway in P. aeruginosa-infected cornea
and the contribution of costimulatory signaling by this pathway to
disease pathology. After bacterial challenge, the number of LC
infiltrating the central cornea was compared in susceptible C57BL/6
(B6) vs resistant (cornea heals) BALB/c mice. LC were more numerous at
1 and 6 days postinfection (p.i.), but were similar at 4 days p.i., in
susceptible vs resistant mice. Mature, B7 positive-stained LC in the
cornea and pseudomonas Ag-associated LC in draining cervical lymph
nodes also were increased significantly p.i. in susceptible mice. To
test the relevance of these data, B6 mice were treated systemically and
subconjunctivally with neutralizing B7 (B7-1/B7-2) mAbs. Treatment
decreased corneal disease severity and reduced significantly the number
of B7-positive cells as well as the recruitment and activation of
CD4+ T cells in the cornea. IFN-
mRNA levels also were
decreased significantly in the cornea and in draining cervical lymph
nodes of mAb-treated mice. When CD28-/- animals were
tested, they exhibited a less severe disease response (no corneal
perforation) than wild-type B6 mice and had a significantly lower
delayed-type hypersensitivity response to heat-killed pseudomonas Ag.
These results support a critical role for B7/CD28 costimulation in
susceptibility to P. aeruginosa ocular
infection.
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L. D. Hazlett, S. A. McClellan, X. L. Rudner, and R. P. Barrett The Role of Langerhans Cells in Pseudomonas aeruginosa Infection Invest. Ophthalmol. Vis. Sci., January 1, 2002; 43(1): 189 - 197. [Abstract] [Full Text] [PDF] |
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