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  • The American Association of Immunologists  (3)
  • 1
    Online Resource
    Online Resource
    The American Association of Immunologists ; 2009
    In:  The Journal of Immunology Vol. 182, No. 1_Supplement ( 2009-04-01), p. 133.33-133.33
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 182, No. 1_Supplement ( 2009-04-01), p. 133.33-133.33
    Abstract: While the development of an efficacious vaccine against TB remains a global priority, the mechanisms of protection and reasons for variability of the BCG vaccine remain poorly understood. Several studies suggest that variation in host genes can affect susceptibility to TB infection. We hypothesized that variation in innate immunity genes is associated with altered immune responses to BCG and its clinical efficacy. Infants (N=12000) were vaccinated at birth with BCG and followed prospectively in a nested case-control study to identify those with active TB and exposed individuals who did not develop disease. Blood samples were collected and re-stimulated with BCG to assess innate and T cell responses. We are examining single nucleotide polymorphisms in TLR pathway genes to determine which variants are associated with BCG-induced cytokine responses. In preliminary analyses, individuals with TLR1 deficiency (TLR1_T1805G) had decreased IL-10 production, but no alteration in IFN-γ or IL-2. Studies are underway to determine whether polymorphisms in 10 additional TLR pathway genes are associated with these responses. To our knowledge, this is the first study to examine whether variation in innate immune genes is associated with different types of BCG-induced immunity. Supported by: Puget Sound Partners for Global Health, the Dana Foundation, and NIH Contract NO1-AI-70022.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 2009
    detail.hit.zdb_id: 1475085-5
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  • 2
    Online Resource
    Online Resource
    The American Association of Immunologists ; 2005
    In:  The Journal of Immunology Vol. 175, No. 3 ( 2005-08-01), p. 1805-1812
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 175, No. 3 ( 2005-08-01), p. 1805-1812
    Abstract: We explored the role of macrophage (Mφ) CD43, a transmembrane glycoprotein, in the pathogenesis of Mycobacterium tuberculosis. Using gene-deleted mice (CD43−/−), we assessed the association of the bacterium with distinct populations of Mφ and found that CD43−/− Mφ bound less M. tuberculosis than CD43+/+ Mφ. Increased infective doses did not abrogate this difference. However, reduced association due to the absence of CD43 could be overcome by serum components. Mφ from heterozygote mice, which express 50% of wild-type CD43, bound more bacteria than CD43−/− but less than CD43+/+, proving that the gene dose of CD43 correlates with binding of M. tuberculosis. Furthermore, the reduced ability of CD43−/− Mφ to bind bacteria was restricted to mycobacterial species. We also found that the survival and replication of M. tuberculosis within Mφ was enhanced significantly in the absence of CD43, making this the first demonstration that the mechanism of mycobacterial entry influences its subsequent growth. Most importantly, we show here that the absence of CD43 in mice aerogenically infected with M. tuberculosis results in an increased bacterial load during both the acute and chronic stages of infection and more rapid development of granulomas, with greater lung involvement and distinctive cellularity.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 2005
    detail.hit.zdb_id: 1475085-5
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  • 3
    Online Resource
    Online Resource
    The American Association of Immunologists ; 2012
    In:  The Journal of Immunology Vol. 188, No. 1_Supplement ( 2012-05-01), p. 125.16-125.16
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 188, No. 1_Supplement ( 2012-05-01), p. 125.16-125.16
    Abstract: Cytokine storm (Hypercytokinemia/Cytokine Release Syndrome) is an acute immune reaction consisting of a positive feedback loop between cytokines and immune cells, resulting in severe inflammation and organ failure. A clinical trial of immunotherapeutic anti-CD28 antibody TGN1412 in 2006 demonstrated the importance of thorough pre-clinical screening and need for more sensitive assays to predict cytokine storm. In that study, 6 healthy volunteers suffered from hypercytokinemia at doses 500-fold less than the lowest dose tested in non-human primates (NHP), showing the failure of standard pre-clinical safety approaches of that time. We have developed an in vitro assay to evaluate antibodies for induction of cytokine storm. Frozen PBMC from humans and NHP are cultured with test articles bound to the cell-culture plate and assayed for cytokine production and cell proliferation. Anti-CD28 superagonist antibodies, which have been shown to stimulate human PBMCs using similar mechanisms as TGN1412, are used as a positive control. Human PBMC produced significantly more IL-2, IL-6, IFN-gamma, TNF-alpha, MIP-1-alpha and several other cytokines compared to isotype control or untreated cells, while PBMC from NHP were non-responsive. The increased production of key pro-inflammatory cytokines in response to stimulation with anti-CD28 antibodies is accompanied by increased PBMC proliferation, while no proliferation increase is detected in isotype-treated or unstimulated human PBMC.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 2012
    detail.hit.zdb_id: 1475085-5
    Location Call Number Limitation Availability
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