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Ectopic lymphoid tissue formation in the lungs of mice infected with Chlamydia pneumoniae is associated with epithelial macrophage inflammatory protein-2/CXCL2 expression

Fitch, Paul; Wheelhouse, Nick; Bowles, P; Paterson, M; Longbottom, David; Entrican, Gary; Howie, Sarah

Authors

Paul Fitch

P Bowles

M Paterson

David Longbottom

Gary Entrican

Sarah Howie



Abstract

Infection with Chlamydia pneumoniae (Cp) accounts for around 10% of community acquired bacterial pneumonia and has been associated with other chronic inflammatory conditions. We describe a C57/Bl6 murine model of Cp lung infection characterized by a dose-dependent, resolving neutrophilia followed by lymphocytic infiltration of the lungs. By 21 days post-infection, mice exhibit a T helper type 1 (Th1) polarized serum antibody response with local mucosal antibody secretion and organization of ectopic lymphoid tissue which persisted in the absence of detectable Cp DNA. Macrophage inflammatory protein (MIP)-2/CXCL2, which recruits neutrophils and lymphocytes and is associated with ectopic lymphoid tissue formation, was secreted in the lungs post-infection. In vitro, lung epithelial cells up-regulated MIP-2/CXCL2 in response to both rough lipopolysaccharide (reLPS) and Cp infection. We conclude that Cp infection can have long-term inflammatory effects on tissue that persist after clearance of active infection.

Citation

Fitch, P., Wheelhouse, N., Bowles, P., Paterson, M., Longbottom, D., Entrican, G., & Howie, S. (2010). Ectopic lymphoid tissue formation in the lungs of mice infected with Chlamydia pneumoniae is associated with epithelial macrophage inflammatory protein-2/CXCL2 expression. Clinical and Experimental Immunology, 162(2), 372-378. https://doi.org/10.1111/j.1365-2249.2010.04231.x

Journal Article Type Article
Acceptance Date Jun 24, 2010
Online Publication Date Sep 14, 2010
Publication Date Oct 8, 2010
Deposit Date Jul 21, 2016
Journal Clin Exp Immunol
Print ISSN 0009-9104
Electronic ISSN 1365-2249
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 162
Issue 2
Pages 372-378
DOI https://doi.org/10.1111/j.1365-2249.2010.04231.x
Keywords Chlamydia pneumoniae, CXCL2/MIP-2, epithelium, lung, lymphocytes,
Public URL http://researchrepository.napier.ac.uk/Output/304717
Related Public URLs http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996604/pdf/cei0162-0372.pdf