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PMID: 10711697 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Increased severity of Pseudomonas aeruginosa corneal infection in strains of mice designated as Th1 versus Th2 responsive.

Investigative ophthalmology & visual science ·Vol. 41 ·No. 3 ·2000-03-00 ·Pages 805-10

Hazlett LD, McClellan S, Kwon B, Barrett R

Abstract

Mice favoring Th1 (C57BL/6, C57BL/10, and B10.D2/nSn) versus Th2 (BALB/c, BALB/cBy, BALB.B, and BALB.K) response development were evaluated for their response to infection with Pseudomonas aeruginosa. This study addresses the question of whether Th1 versus Th2 response propensity affects the pathogenesis of bacterial keratitis in mice. Ocular disease was determined by mean clinical score, slit lamp, plate counts, and histopathology, and antigen-specific cellular responses were assessed by immunostaining and measurement of delayed type hypersensitivity (DTH). Strains of mice favoring Th1 (B6, BL10, and B10.D2) versus Th2 (BALB/c, BALB/cBy, BALB.B, and BALB.K) responsiveness were infected with P. aeruginosa. Mice favoring Th1 response development exhibited a similar course of disease and the infected eyes of all mice perforated by 7 days postinfection (p.i.). Strains (BALB/c, BALB/cBy, BALB.B, and BALB.K) favoring Th2 response development exhibited a milder course of disease, and none of the infected corneas perforated at 7 days p.i. In a Th1-responsive strain (B10.D2), positive immunostaining for CD4+ and CD8+ T cells was observed in the cornea by 3 days p.i. and by 5 days p.i., respectively, some cells stained positively for IL2-R, indicating that the cells were activated. In contrast, in a Th2 responder strain (BALB/c), there was no detectable positive immunostaining in cornea for any of the T-cell markers tested and DTH was significantly elevated in B10.D2 versus BALB/c mice. These studies are the first to provide evidence that in P. aeruginosa ocular infection, mouse strains favoring development of a Th1-type response are susceptible (cornea perforates), whereas strains favoring Th2 response development are resistant (no corneal perforation).

MeSH Terms
Animals CD4 Antigens/metabolism CD4-Positive T-Lymphocytes/immunology,metabolism,pathology CD8 Antigens/metabolism CD8-Positive T-Lymphocytes/immunology,metabolism,pathology Cornea/immunology,microbiology,pathology Eye Infections, Bacterial/immunology,metabolism,pathology Female Hypersensitivity, Delayed/immunology Immunoenzyme Techniques Keratitis/immunology,metabolism,pathology Mice Mice, Inbred BALB C Mice, Inbred C57BL Pseudomonas Infections/immunology,metabolism,pathology Pseudomonas aeruginosa Receptors, Interleukin-2/metabolism Rupture, Spontaneous Th1 Cells/immunology,metabolism Th2 Cells/immunology,metabolism
Chemicals
CD4 Antigens CD8 Antigens Receptors, Interleukin-2
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hazlett L D
Department of Anatomy/Cell Biology, Wayne State University School of Medicine, Detroit, Michigan 48201, USA. lhazlett@med.wayne.edu
McClellan S
Kwon B
Barrett R
Article Info
Journal
Investigative ophthalmology & visual science
Abbr.
Invest Ophthalmol Vis Sci
ISSN
0146-0404
Published
2000-03-00
Pages
805-10
Language
English
Region
United States
NLM ID
7703701
Subset
IM
Grants
NEI NIH HHS · P30EY04068 · United States
NEI NIH HHS · R01EY02986 · United States
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