Authors: | Flynn, J. L.; Goldstein, M. M.; Chan, J.; Triebold, K. J.; Pfeffer, K.; Lowenstein, C. J.; Schrelber, R.; Mak, T. W.; Bloom, B. R. |
Article Title: | Tumor necrosis factor-α is required in the protective immune response against mycobacterium tuberculosis in mice |
Abstract: | Understanding the immunological mechanisms of protection and pathogenesis in tuberculosis remains problematic. We have examined the extent to which tumor necrosis factor-α (TNFα) contributes to this disease using murine models In which the action of TNFα is inhibited. TNFa was neutralized In vivo by monoclonal antibody; in addition, a mouse strain with a disruption in the gene for the 55 kDa TNF receptor was used. The data from both models established that TNFα and the 55 kDa TNF receptor are essential for protection against tuberculosis in mice, and for reactive nitrogen production by macrophages early in infection. Granulomas were formed in equal numbers in control and experimental mice, but necrosis was observed only in mice deficient in TNFα or TNF receptor. TNFα and the 55 kDa TNF receptor are necessary conditions for protection against murine M. tuberculosis infection, but are not solely responsible for the tissue damage observed. © 1995. |
Keywords: | immunohistochemistry; controlled study; nonhuman; polymerase chain reaction; mouse; animal; mice; bcg vaccine; animal experiment; animal model; mice, inbred c57bl; antibodies, monoclonal; mycobacterium tuberculosis; immune response; tumor necrosis factor alpha; lung; tumor necrosis factor receptor; macrophage; tuberculosis; granuloma; tumor necrosis factor; immunization; receptors, tumor necrosis factor; nitric-oxide synthase; female; priority journal; article; amino acid oxidoreductases |
Journal Title: | Immunity |
Volume: | 2 |
Issue: | 6 |
ISSN: | 1074-7613 |
Publisher: | Cell Press |
Date Published: | 1995-06-01 |
Start Page: | 561 |
End Page: | 572 |
Language: | English |
DOI: | 10.1016/1074-7613(95)90001-2 |
PUBMED: | 7540941 |
PROVIDER: | scopus |
DOI/URL: | |
Notes: | Article -- Export Date: 28 August 2018 -- Source: Scopus |