Exposure to Cigarette Smoke Inhibits the Pulmonary T-Cell Response to Influenza Virus and Mycobacterium tuberculosis

Author:

Feng Yan1,Kong Ying1,Barnes Peter F.12,Huang Fang-Fang1,Klucar Peter13,Wang Xisheng1,Samten Buka12,Sengupta Mayami14,Machona Bruce15,Donis Ruben6,Tvinnereim Amy R.1,Shams Homayoun12

Affiliation:

1. Center for Pulmonary and Infectious Disease Control, The University of Texas Health Science Center at Tyler, Tyler, Texas 75708

2. Departments of Microbiology and Immunology, The University of Texas Health Science Center at Tyler, Tyler, Texas 75708

3. Present address: Baylor Institute for Immunology Research, 3434 Live Oak St., Dallas, TX 75204.

4. Present address: Department of Pediatrics, Albert Einstein College of Medicine, Bronx, NY 10461.

5. Present address: Department of Biological Sciences, CW 405, Biological Sciences Bldg., University of Alberta, Edmonton, Alberta, Canada T6G 2E9.

6. Influenza Division, Centers for Disease Control and Prevention, 1600 Clifton Rd., Atlanta, Georgia 30333

Abstract

ABSTRACT Smoking is associated with increased susceptibility to tuberculosis and influenza. However, little information is available on the mechanisms underlying this increased susceptibility. Mice were left unexposed or were exposed to cigarette smoke and then infected with Mycobacterium tuberculosis by aerosol or influenza A by intranasal infection. Some mice were given a DNA vaccine encoding an immunogenic M. tuberculosis protein. Gamma interferon (IFN-γ) production by T cells from the lungs and spleens was measured. Cigarette smoke exposure inhibited the lung T-cell production of IFN-γ during stimulation in vitro with anti-CD3, after vaccination with a construct expressing an immunogenic mycobacterial protein, and during infection with M. tuberculosis and influenza A virus in vivo . Reduced IFN-γ production was mediated through the decreased phosphorylation of transcription factors that positively regulate IFN-γ expression. Cigarette smoke exposure increased the bacterial burden in mice infected with M. tuberculosis and increased weight loss and mortality in mice infected with influenza virus. This study provides the first demonstration that cigarette smoke exposure directly inhibits the pulmonary T-cell response to M. tuberculosis and influenza virus in a physiologically relevant animal model, increasing susceptibility to both pathogens.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference47 articles.

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2. Benowitz, N. L. 2010. Secondhand smoke and infectious disease in adults: a global women's health concern: comment on “passive smoking and tuberculosis.” Arch. Intern. Med. 170:292-293.

3. Boom, W. H. 1996. The role of T-cell subsets in Mycobacterium tuberculosis infection. Infect. Agents Dis. 5:73-81.

4. Brown, D. M., A. M. Dilzer, D. L. Meents, and S. L. Swain. 2006. CD4 T cell-mediated protection from lethal influenza: perforin and antibody-mediated mechanisms give a one-two punch. J. Immunol. 177:2888-2898.

5. Caruso, A. M., N. Serbina, E. Klein, K. Triebold, B. R. Bloom, and J. L. Flynn. 1999. Mice deficient in CD4 T cells have only transiently diminished levels of IFN-gamma, yet succumb to tuberculosis. J. Immunol. 162:5407-5416.

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