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PMID: 9486397 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Phenotypic changes in T cell populations during the reactivation of tuberculosis in mice.

Clinical and experimental immunology ·Vol. 111 ·No. 2 ·1998-02-00 ·Pages 309-15

Howard AD, Trask OJ, Weisbrode SE, Zwilling BS

Abstract

The phenotypic changes of T lymphocytes during the reactivation of latent Mycobacterium tuberculosis infection by activation of the hypothalamic-pituitary-adrenal (HPA) axis was monitored using flow cytometric analysis. Subsets of CD4+ and CD8+ lymphocyte populations from the lung, spleen and draining lymph nodes of infected mice were identified based on their differential expression of the cell surface antigens CD44 and CD45RB. Latent infection was characterized by an accumulation of both naive, activated and memory CD4 and CD8 T lymphocytes in the lung and mediastinal lymph nodes. No changes were observed in the spleen of mice with latent infection when compared with uninfected mice. Immediately following the activation of the HPA axis, a reduction in all CD4+ and CD8+ T cells in the lung and mediastinal lymph nodes was observed. This correlated with the reactivation of mycobacterial growth. The decrease was transient for memory and naive CD4 and CD8 T lymphocyte populations in the lung. However, the number of naive CD4 and CD8 T lymphocyte populations in the mediastinal lymph node following reactivation was less than that found in mice with latent infection. These data provide the first characterization of T lymphocyte populations which may be functionally involved in the immunological response to HPA axis-induced reactivation of M. tuberculosis infection.

MeSH Terms
Animals CD4-CD8 Ratio CD8-Positive T-Lymphocytes/immunology Flow Cytometry Hyaluronan Receptors/immunology Hypothalamo-Hypophyseal System/immunology,physiology Immunologic Memory/immunology Leukocyte Common Antigens/immunology Lymphocyte Activation Male Mice Mice, Inbred BALB C Mycobacterium tuberculosis Phenotype Pituitary-Adrenal System/immunology,physiology Pneumonia, Bacterial/immunology,microbiology T-Lymphocyte Subsets/immunology T-Lymphocytes/immunology Tuberculosis, Pulmonary/immunology
Chemicals
Hyaluronan Receptors Leukocyte Common Antigens
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Howard A D
Department of Microbiology, Ohio State University, Columbus 43210, USA.
Trask O J
Weisbrode S E
Zwilling B S
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Article Info
Journal
Clinical and experimental immunology
Abbr.
Clin Exp Immunol
ISSN
0009-9104
Published
1998-02-00
Pages
309-15
Language
English
Region
England
NLM ID
0057202
PMCID
PMC1904909
Subset
IM
Grants
NCI NIH HHS · P30 CA016058 · United States
NCI NIH HHS · CA16058 · United States
NIMH NIH HHS · MH45679 · United States
NIMH NIH HHS · MH54966 · United States
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