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Publication : IL-12 increases resistance of BALB/c mice to Mycobacterium tuberculosis infection.

First Author  Flynn JL Year  1995
Journal  J Immunol Volume  155
Issue  5 Pages  2515-24
PubMed ID  7650381 Mgi Jnum  J:28196
Mgi Id  MGI:75821 Doi  10.4049/jimmunol.155.5.2515
Citation  Flynn JL, et al. (1995) IL-12 increases resistance of BALB/c mice to Mycobacterium tuberculosis infection. J Immunol 155(5):2515-24
abstractText  IL-12, a cytokine produced by macrophages and B cells, has recently been found to exert pleiotropic effects on the immune system. When BALB/c mice, a strain highly susceptible to virulent Mycobacterium tuberculosis infection, were given IL-12 at the initiation of infection with M. tuberculosis, their mean survival time doubled from 58 to 112 days. IL-12-treated mice had diminished bacterial burdens, whereas treatment with exogenous IFN-gamma had no effect on survival or bacterial burden. IL-12 treatment also delayed lung pathology in BALB/c mice. In contrast with the findings in the BALB/c model, IL-12 did not increase survival of M. tuberculosis-infected gko mice, transgenic mice in which the IFN-gamma gene has been disrupted, indicating that IL-12 does not induce protection against tuberculosis in mice in the absence of IFN-gamma.
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