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Interferon-γ-producing immature myeloid cells confer protection against severe invasive group A Streptococcus infections

Takayuki Matsumura, Manabu Ato (), Tadayoshi Ikebe, Makoto Ohnishi, Haruo Watanabe and Kazuo Kobayashi
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Takayuki Matsumura: National Institute of Infectious Diseases
Manabu Ato: National Institute of Infectious Diseases
Tadayoshi Ikebe: National Institute of Infectious Diseases
Makoto Ohnishi: National Institute of Infectious Diseases
Haruo Watanabe: National Institute of Infectious Diseases
Kazuo Kobayashi: National Institute of Infectious Diseases

Nature Communications, 2012, vol. 3, issue 1, 1-11

Abstract: Abstract Cytokine-activated neutrophils are known to be essential for protection against group A Streptococcus infections. However, during severe invasive group A Streptococcus infections that are accompanied by 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 group A Streptococcus isolates, but not with non-invasive group A Streptococcus isolates, exhibit high concentrations of plasma interferon-γ during the early stage of infection. Interferon-γ is necessary to protect mice, and is produced by a novel population of granulocyte–macrophage colony-stimulating factor-dependent immature myeloid cells with ring-shaped nuclei. These interferon-γ-producing immature myeloid cells express monocyte and granulocyte markers, and also produce nitric oxide. The adoptive transfer of interferon-γ-producing immature myeloid cells ameliorates infection in wild-type and interferon-γ-deficient mice. Our results indicate that interferon-γ-producing immature myeloid cells have a protective role during the early stage of severe invasive group A Streptococcus infections.

Date: 2012
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DOI: 10.1038/ncomms1677

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