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. 1998 Mar;66(3):927-31.
doi: 10.1128/IAI.66.3.927-931.1998.

Protein deficiency induces alterations in the distribution of T-cell subsets in experimental pulmonary tuberculosis

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Protein deficiency induces alterations in the distribution of T-cell subsets in experimental pulmonary tuberculosis

E S Mainali et al. Infect Immun. 1998 Mar.

Abstract

Previous research has suggested that dietary protein deficiency alters resistance to experimental pulmonary tuberculosis, in part, by affecting the distribution and trafficking of antigen-reactive T cells. In this study, guinea pigs were maintained on either a protein-deficient (10% ovalbumin) or control (30% ovalbumin) diet and infected 4 to 6 weeks later with a low dose of virulent Mycobacterium tuberculosis H37Rv by the respiratory route. Monoclonal antibodies directed against the CD4 or CD8 markers on guinea pig lymphocytes were used in a flow cytofluorometric assay to determine the proportion of each subset in the peripheral circulation, spleen, and bronchotracheal lymph nodes at 4 weeks after infection. In uninfected guinea pigs, only the spleen exhibited an effect of diet on T-cell distribution, with small but consistent reductions in the proportions of both CD4 and CD8 T lymphocytes. However, following infection, protein deficiency exerted a profound effect on T-cell distribution. Malnourished, tuberculous guinea pigs harbored only 20 and 60% of the T cells (as a proportion of total lymphoid cells) found in the spleen and blood, respectively, of their well-nourished counterparts. Normal relative proportions of CD4 and CD8 cells were observed, however. In striking contrast, the bronchotracheal lymph nodes of protein-deprived guinea pigs with tuberculosis contained more than twice the numbers of T cells of control guinea pigs, and the normal CD4-to-CD8 ratio was reversed. Peripheral T-cell function, as measured by the delayed hypersensitivity skin test to tuberculin, and antigen-induced lymphoproliferation in vitro were markedly suppressed in protein-malnourished animals. Conversely, purified protein derivative-induced (but not concanavalin A-induced) proliferation was significantly enhanced in cultures of lymph node cells from protein-deprived tuberculous animals. Taken together, these results suggest that immunological abnormalities and loss of antimycobacterial resistance in the lungs of protein-deficient guinea pigs may be explained, in part, by sequestration of antigen-reactive T cells in the lymph nodes draining the site of infection.

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Figures

FIG. 1
FIG. 1
Effect of diet on the percentages of lymphocytes expressing αβTcR, CD4, or CD8 markers in the spleen and blood of strain 2 guinea pigs fed a C or LP diet for 4 weeks and infected for an additional 4 weeks with virulent M. tuberculosis H37Rv by the respiratory route. Data are based upon flow cytofluorometric analysis of 10,000 events and are means ± standard errors of the means for five to seven animals per treatment.
FIG. 2
FIG. 2
Influence of diet on the percentages of lymphocytes bearing αβTcR, CD4, or CD8 phenotypic markers in the bronchotracheal lymph nodes of strain 2 guinea pigs fed a C or LP diet for 4 weeks and infected by the pulmonary route with virulent M. tuberculosis H37Rv for an additional 4 weeks. Data are based upon flow cytofluorometric analysis of 10,000 events and are means ± standard errors of the means for five to seven animals per treatment.

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