2013 Fiscal Year Final Research Report
The protective role of a novel population of interferon-gamma-producing cells in severe invasive group A streptococcal infections
Project/Area Number |
22790959
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Infectious disease medicine
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Research Institution | National Institute of Infectious Diseases |
Principal Investigator |
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Project Period (FY) |
2010-04-01 – 2014-03-31
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Keywords | 感染症防御学 / 劇症型溶血性レンサ球菌感染症 / IFN-γ |
Research Abstract |
Cytokine-activated neutrophils are known to be essential for protection against group A Streptococcus (GAS) infections. However, during severe invasive GAS infections that accompanied with neutropenia, it remains unclear which factors are protective against such infections, and which cell population is the source of them. Here we show that mice infected with severe invasive GAS isolates, but not with non-invasive GAS isolates, exhibit high concentrations of plasma IFN-g during the early stage of infection. IFN-g is necessary to protect mice, and is produced by a novel population of GM-CSF-dependent immature myeloid cells with ring-shaped nuclei (IFN-g-producing immature myeloid cells; gIMCs). These gIMCs express monocyte and granulocyte markers, and also produce nitric oxide. The adoptive transfer of gIMCs ameliorates infection in wild-type and IFN-g-deficient mice. Our results indicate that gIMCs have a protective role during the early stage of severe invasive GAS infections.
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[Journal Article] Critical roles for lipomannan and lipoarabinomannan in cell wall integrity of mycobacteria and pathogenesis of tuberculosis2013
Author(s)
Fukuda T, Matsumura T, Ato M, Hamasaki M, Nishiuchi Y, Murakami Y, Maeda Y, Yoshimori T, Matsumoto S, Kobayashi K, Kinoshita T, Morita YS
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DOI
Peer Reviewed
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