This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Allen, S. S.
Right arrow Articles by McMurray, D. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Allen, S. S.
Right arrow Articles by McMurray, D. N.

 Previous Article  |  Next Article 

Infection and Immunity, August 2003, p. 4271-4277, Vol. 71, No. 8
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.8.4271-4277.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Coordinate Cytokine Gene Expression In Vivo following Induction of Tuberculous Pleurisy in Guinea Pigs

Shannon Sedberry Allen* and David N. McMurray

Department of Medical Microbiology & Immunology, Texas A&M University System Health Science Center, College Station, Texas 77843

Received 25 February 2003/ Returned for modification 2 April 2003/ Accepted 29 April 2003

Tuberculous pleurisy is a severe inflammatory response induced by Mycobacterium tuberculosis organisms that have escaped from lung granulomata into the pleural space during pulmonary infection. We have used the guinea pig model of tuberculous pleurisy to examine several aspects of the immune response to this antigen-specific inflammatory event. Pleurisy was induced by injection of heat-killed M. tuberculosis H37Rv directly into the pleural space of guinea pigs previously vaccinated with M. bovis BCG. Four animals were euthanized each day over a period of 9 days. Fluid in the pleural cavity was analyzed for transforming growth factor ß1 (TGF-ß1) and total interferon (IFN) protein levels. In addition, RNA was obtained from pleural cells and examined for TGF-ß1, tumor necrosis factor alpha (TNF-{alpha}), IFN-{gamma}, and interleukin-8 (IL-8) expression by real-time PCR. Finally, pleural cells were examined for the ability to proliferate in response to concanavalin A and purified protein derivative (PPD) in vitro. In the pleural fluid, TGF-ß1 protein concentrations increased over the course of the inflammatory response while IFN protein levels were not significantly altered. Expression of TGF-ß1 mRNA peaked on days 3 and 4, and IFN-{gamma} mRNA expression peaked on day 3 and then returned to background levels. TNF-{alpha} mRNA expression was highest on days 2 to 4, and IL-8 mRNA levels remained elevated between days 2 and 5, peaking on day 3 before returning to background levels. PPD-induced proliferative responses were evident by day 3 and remained present throughout the study. Analysis of cytokine expression during tuberculous pleurisy may lead to a better understanding of the self-healing nature of this manifestation of tuberculosis.


* Corresponding author. Mailing address: Department of Medical Microbiology and Immunology, Texas A&M University System Health Science Center, 407 Reynolds Medical Building, College Station, TX 77843-1114. Phone: (979) 845-3679. Fax: (979) 845-3479. E-mail: sedberry{at}medicine.tamu.edu.

Editor: S. H. E. Kaufmann


Infection and Immunity, August 2003, p. 4271-4277, Vol. 71, No. 8
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.8.4271-4277.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Grover, A., Taylor, J., Troudt, J., Keyser, A., Arnett, K., Izzo, L., Rholl, D., Izzo, A. (2009). Kinetics of the Immune Response Profile in Guinea Pigs after Vaccination with Mycobacterium bovis BCG and Infection with Mycobacterium tuberculosis. Infect. Immun. 77: 4837-4846 [Abstract] [Full Text]  
  • Souza, M. C., Penido, C., Costa, M. F. S., Henriques, M. G. (2008). Mechanisms of T-Lymphocyte Accumulation during Experimental Pleural Infection Induced by Mycobacterium bovis BCG. Infect. Immun. 76: 5686-5693 [Abstract] [Full Text]  
  • McFarland, C. T., Fan, Y.-Y., Chapkin, R. S., Weeks, B. R., McMurray, D. N. (2008). Dietary Polyunsaturated Fatty Acids Modulate Resistance to Mycobacterium tuberculosis in Guinea Pigs. J. Nutr. 138: 2123-2128 [Abstract] [Full Text]  
  • Ly, L. H., Russell, M. I., McMurray, D. N. (2008). Cytokine Profiles in Primary and Secondary Pulmonary Granulomas of Guinea Pigs with Tuberculosis. Am. J. Respir. Cell Mol. Bio. 38: 455-462 [Abstract] [Full Text]  
  • Sawant, K. V., McMurray, D. N. (2007). Guinea Pig Neutrophils Infected with Mycobacterium tuberculosis Produce Cytokines Which Activate Alveolar Macrophages in Noncontact Cultures. Infect. Immun. 75: 1870-1877 [Abstract] [Full Text]  
  • Tree, J. A., Elmore, M. J., Javed, S., Williams, A., Marsh, P. D. (2006). Development of a Guinea Pig Immune Response-Related Microarray and Its Use To Define the Host Response following Mycobacterium bovis BCG Vaccination. Infect. Immun. 74: 1436-1441 [Abstract] [Full Text]  
  • Cho, H., McMurray, D. N. (2005). Neutralization of Tumor Necrosis Factor Alpha Suppresses Antigen-Specific Type 1 Cytokine Responses and Reverses the Inhibition of Mycobacterial Survival in Cocultures of Immune Guinea Pig T Lymphocytes and Infected Macrophages. Infect. Immun. 73: 8437-8441 [Abstract] [Full Text]  
  • Kang, H., Gross, D. C. (2005). Characterization of a Resistance-Nodulation-Cell Division Transporter System Associated with the syr-syp Genomic Island of Pseudomonas syringae pv. syringae. Appl. Environ. Microbiol. 71: 5056-5065 [Abstract] [Full Text]  
  • Mehal, W. Z., Sheikh, S. Z., Gorelik, L., Flavell, R. A. (2005). TGF-{beta} signaling regulates CD8+ T cell responses to high- and low-affinity TCR interactions. Int Immunol 17: 531-538 [Abstract] [Full Text]  
  • Skwor, T. A., Cho, H., Cassidy, C., Yoshimura, T., McMurray, D. N. (2004). Recombinant guinea pig CCL5 (RANTES) differentially modulates cytokine production in alveolar and peritoneal macrophages. J. Leukoc. Biol. 76: 1229-1239 [Abstract] [Full Text]  
  • Allen, S. S., Cassone, L., Lasco, T. M., McMurray, D. N. (2004). Effect of Neutralizing Transforming Growth Factor {beta}1 on the Immune Response against Mycobacterium tuberculosis in Guinea Pigs. Infect. Immun. 72: 1358-1363 [Abstract] [Full Text]