Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993 Jul;61(7):2841-7.
doi: 10.1128/iai.61.7.2841-2847.1993.

Cytokine response of T-cell subsets from Brucella abortus-infected mice to soluble Brucella proteins

Affiliations

Cytokine response of T-cell subsets from Brucella abortus-infected mice to soluble Brucella proteins

Y Zhan et al. Infect Immun. 1993 Jul.

Abstract

Hot saline extracts of Brucella abortus 19 were separated by successive differential precipitation with 50 and 70% ammonium sulfate, yielding fractions SBP50, with predominantly 36-kDa proteins and a number of medium-sized proteins (26 to 33 kDa), and SBP70, with 14-kDa and lower-molecular-mass proteins. Both fractions stimulated specifically proliferation and cytokine production by spleen cells from brucella-infected mice, although the activity of SBP50 was much higher than that of SBP70. Further separation of SBP50 by a DEAE-Sepharose column resulted in three distinct subfractions which were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The three subfractions were analyzed for their abilities to induce lymphocytes to proliferate and produce cytokines. The three subfractions were all active but with characteristic differences in magnitude. Subfraction 1 stimulated moderate proliferation, high interleukin 6 (IL-6) production, and relatively low production of gamma interferon (IFN-gamma). Subfraction 2 was the strongest stimulus for proliferation and production of IL-6 and IFN-gamma, while subfraction 3 stimulated moderate cell proliferation, a high level of IFN-gamma, and a low level of IL-6. IL-2 production stimulated by the three subfractions was similar. SBP50 and all three subfractions stimulated purified T cells of both CD4+ and CD8+ subsets to produce IFN-gamma. The production of IFN-gamma by CD8+ T cells to brucella antigens was enhanced with exogenous IL-2.

PubMed Disclaimer

References

    1. Rev Infect Dis. 1983 Sep-Oct;5(5):821-42 - PubMed
    1. Immunol Rev. 1983;74:29-56 - PubMed
    1. Eur J Immunol. 1984 Oct;14(10):964-7 - PubMed
    1. Proc Natl Acad Sci U S A. 1985 Nov;82(21):7404-8 - PubMed
    1. Vet Immunol Immunopathol. 1985 Aug;9(4):383-96 - PubMed

Publication types