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Diversity of Lung and Spleen Immune Responses in Mice with Slowly Progressive Primary Tuberculosis
Author(s) -
Phyu,
Tadesse,
Mustafa,
Tadesse,
Jønsson,
Bjune
Publication year - 2000
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1046/j.1365-3083.2000.00662.x
Subject(s) - spleen , cytokine , immune system , lung , concanavalin a , immunology , mycobacterium tuberculosis , tuberculosis , interferon gamma , biology , interleukin 4 , t cell , interleukin 2 , pathology , medicine , in vitro , biochemistry
The aim of the present study was to assess the compartmentalized immune response, in terms of cytokine secretion and cell activation, in lungs and spleens of mice with slowly progressive primary tuberculosis. Immunocyte populations from both organs were isolated and stimulated with concanavalin A, purified protein derivatives and MPT 59. Production of interferon‐γ (IFN‐γ) and interleukin‐4 (IL‐4) was measured using an enzyme‐linked immunosorbent assay, and cell activation was measured using a tetrazolium colorimetric assay. The IFN‐γ and IL‐4 levels in the supernatants of Mycobacterium tuberculosis antigen (Ag)‐stimulated lung immunocytes from infected mice were higher than the levels from uninfected mice. However, only IL‐4 levels were raised in the supernatants of Ag‐stimulated spleen immunocytes from infected mice. Spontaneous and Ag‐stimulated immunocyte activation was lower only in the lungs of infected mice compared with uninfected mice. The level of lung immunocyte activation was inversely associated with the extent of gross pulmonary pathology. In conclusion, cytokine secretion and cell activation were different between lungs and spleens in slowly progressive primary murine tuberculosis. Cytokine diversity may explain the confinement of tuberculous lesions in the lungs and the absence of lesions in the spleens of mice with slowly progressive tuberculosis.