首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Selective Protection against Conidia by Mononuclear and against Mycelia by Polymorphonuclear Phagocytes in Resistance to Aspergillus
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Selective Protection against Conidia by Mononuclear and against Mycelia by Polymorphonuclear Phagocytes in Resistance to Aspergillus

机译:单核细胞对分生孢子的选择性保护和多形核吞噬细胞对曲霉菌的选择性保护。

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摘要

By comparing natural immunity to Aspergillus fumigatus (AF) in vivo with the action of human or mouse phagocytes against AF in vitro, we delineated two sequential lines of defense against AF. The first line of defense was formed by macrophages and directed against spores. Macrophages prevented germination and killed spores in vitro and rapidly eradicated conidia in vivo, even in neutropenic and athymic mice. The second was the neutrophilic granulocyte (PMN), which protected against the hyphal form of AF. Human and mouse PMN killed mycelia in vitro. Normal, but not neutropenic mice, stopped hyphal growth, and eradicated mycelia. Either line of defense acting alone protected mice from high challenge doses. Natural immunity collapsed only when both the reticuloendothelial system and PMN were impaired. These findings are in keeping with the clinical observation that high doses of cortisone and neutropenia are the main risk factors for invasive aspergillosis. Cortisone inhibited the conidiacidal activity of mouse macrophages in vivo and of human or mouse mononuclear phagocytes in vitro. Cortisone damaged this first line of defense directly and not through the influence of T lymphocytes or other systems modifying macrophage function as shown in athymic mice and in vitro. In addition, daily high doses of cortisone in mice reduced the mobilization of PMN so that the second line of defense was also impaired. Thus, cortisone can break down natural resistance on its own. Myelosuppression rendered mice susceptible only when the first line of defense was overpowered by high challenge doses, by activated spores that cannot be killed by macrophages, or by cortisone suppression of the conidiacidal activity of macrophages.The host, thus, can call upon two independent phagocytic cell lines that form graded defense systems against aspergillus. These lines of defense function in the absence of a specific immune response, which seems superfluous in the control and elimination of this fungus.
机译:通过比较体内对烟曲霉(AF)的天然免疫力与人或小鼠吞噬细胞在体外对AF的作用,我们划定了两个连续的AF防御线。第一道防线是由巨噬细胞形成的,并针对孢子。巨噬细胞即使在中性粒细胞减少和无胸腺小鼠中,也能在体外阻止发芽并杀死孢子,并在体内迅速消除分生孢子。第二个是嗜中性粒细胞(PMN),它能抵抗菌丝形式的房颤。人和小鼠PMN在体外杀死了菌丝体。正常但非嗜中性白血球减少的小鼠停止了菌丝生长,并消除了菌丝体。任一个防御线都可以保护小鼠免受高剂量的攻击。仅当网状内皮系统和PMN均受损时,自然免疫性才崩溃。这些发现与临床观察一致,即高剂量可的松和中性粒细胞减少是侵袭性曲霉病的主要危险因素。可的松体内抑制小鼠巨噬细胞和体外人或小鼠单核吞噬细胞的蜜二酸活性。可的松直接损害了第一道防线,而不是通过无胸腺小鼠和体外的T淋巴细胞或其他修饰巨噬细胞功能的系统的影响。此外,每天在小鼠中高剂量的可的松会降低PMN的动员,因此第二道防线也会受到损害。因此,可的松可以自行破坏自然抵抗力。只有当第一道防线被高剂量的攻击,不能被巨噬细胞杀死的活化的孢子或可的松抑制巨噬细胞的蜜二酸活性所压倒时,骨髓抑制才使小鼠易感。宿主因此可以召唤两个独立的吞噬细胞形成针对曲霉的分级防御系统的细胞系。这些防御线在没有特异性免疫反应的情况下起作用,这在控制和消除这种真菌上似乎是多余的。

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