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pubmed-article:11454067pubmed:abstractTextWe investigated the role of interleukin-6 (IL-6) in the development of the immune response to a subunit vaccine against tuberculosis consisting of the culture filtrate proteins of Mycobacterium tuberculosis emulsified in the adjuvant dimethyldioctadecylammonium bromide (DDA). C57Bl/6 mice immunized with this vaccine developed a strong T helper 1 (Th1) response characterized by an increased production of interferon-gamma (IFN-gamma) secreted by CD4+ T cells. Neutralization of IL-6 during in vivo priming resulted in marked reduction in the ability of T cells to secrete IFN-gamma and IL-2 and to proliferate. IL-6 gene-disrupted mice primed with the vaccine showed a decrease in the number of IFN-gamma-producing cells and an increase in IL-4-secreting cells as compared to control mice. In contrast, neutralization of IL-6 during a boost of the vaccine in previously primed mice did not affect the development of IFN-gamma-producing cells but still increased the number of IL-4-producing cells. Our work shows that IL-6 plays a major role in the priming but not in the later expression of a Th1 response to a tuberculosis vaccine.lld:pubmed
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pubmed-article:11454067pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:11454067pubmed:articleTitleInterleukin-6 regulates the phenotype of the immune response to a tuberculosis subunit vaccine.lld:pubmed
pubmed-article:11454067pubmed:affiliationLaboratory of Microbiology and Immunology of Infection, Institute for Molecular and Cell Biology, University of Porto, Porto, Portugal.lld:pubmed
pubmed-article:11454067pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11454067pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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