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From the Cover: Innate immune-induced depletion of bone marrow neutrophils aggravates systemic bacterial infections

机译:从封面开始:先天性免疫诱导的骨髓中性粒细胞耗竭加剧了全身细菌感染

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摘要

Neutrophils are the most abundant leukocytes in circulation and provide a primary innate immune defense function against bacterial pathogens before development of a specific immune response. These specialized phagocytes are short lived (12–24 hours) and continuously replenished from bone marrow. We found that if the host is overwhelmed by a high inoculum of Listeria monocytogenes, neutrophils are depleted despite high granulocyte-colony stimulating factor induction. In contrast to a low-dose innocuous L. monocytogenes infection, high-dose Listeria challenge blocks neutrophil recruitment to infectious abscesses and bacterial proliferation is not controlled, resulting in lethal outcomes. Administering synthetic TLR2-ligand or heat-killed bacteria during the innocuous L. monocytogenes infection reproduced these effects, once again leading to overwhelming bacterial propagation. The same stimuli also severely aggravated Salmonella typhimurium, Staphylococcus aureus, and Streptococcus pyogenes systemic infection. These data implicate systemic innate immune stimulation as a mechanism of bone marrow neutrophil exhaustion which negatively influences the outcome of bacterial infections.
机译:中性粒细胞是循环中最丰富的白细胞,并在形成特定的免疫反应之前提供针对细菌病原体的主要先天免疫防御功能。这些专门的吞噬细胞寿命短(12–24小时),并从骨髓中不断补充。我们发现,如果宿主被单核细胞增生性李斯特菌的高接种量所淹没,尽管粒细胞集落刺激因子诱导很高,但中性粒细胞却被耗尽。与小剂量无毒单核细胞增生李斯特氏菌感染相反,大剂量李斯特菌激发可阻止嗜中性白细胞募集至感染性脓肿,并且细菌增殖不受控制,导致致命结果。在无害的单核细胞增生李斯特氏菌感染期间施用合成的TLR2配体或热灭活细菌可重现这些效果,再次导致细菌繁殖异常。相同的刺激也会严重加重鼠伤寒沙门氏菌,金黄色葡萄球菌和化脓性链球菌的全身感染。这些数据暗示全身性先天性免疫刺激是骨髓嗜中性白细胞衰竭的一种机制,对细菌感染的结果产生负面影响。

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