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Alarmins link neutrophils and dendritic cells

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TRENDS IN IMMUNOLOGY
卷 30, 期 11, 页码 531-538

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ELSEVIER SCI LTD
DOI: 10.1016/j.it.2009.07.004

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资金

  1. Deutsche Forschungsgemeinschaft [SO876/3-1, FOR809, WE1913/10-1]
  2. Swedish Research Council
  3. Swedish Heart-Lung Foundation
  4. Lars Hierta Memorial Fund
  5. Karolinska Institute
  6. Interdisciplinary Center for Clinical Research BIOMAT within the Faculty of Medicine at the RWTH Aachen University [VV-B113]

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Neutrophils are the first major population of leukocyte to infiltrate infected or injured tissues and are crucial for initiating host innate defense and adaptive immunity. Although the contribution of neutrophils to innate immune defense is mediated predominantly by phagocytosis and killing of microorganisms, neutrophils also participate in the induction of adaptive immune responses. At sites of infection and/or injury, neutrophils release numerous mediators upon degranulation or death, among these are alarmins which have a characteristic dual capacity to mobilize and activate antigen-presenting cells. We describe here how alarmins released by neutrophil degranulation and/or death can link neutrophils to dendritic cells by promoting their recruitment and activation, resulting in the augmentation of innate and adaptive immune responses.

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