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首页> 外文期刊>Infection and immunity >Macrophages as effector cells of protective immunity in murine schistosomiasis: macrophage activation in mice vaccinated with radiation-attenuated cercariae.
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Macrophages as effector cells of protective immunity in murine schistosomiasis: macrophage activation in mice vaccinated with radiation-attenuated cercariae.

机译:巨噬细胞作为鼠血吸虫病中保护性免疫的效应细胞:接种有辐射衰减尾尾aria的小鼠中的巨噬细胞活化。

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Cell-mediated immune responses contributing to macrophage activation were compared in mice that demonstrated partial resistance to challenge Schistosoma mansoni infection as a result of vaccination with radiation-attenuated cercariae or of ongoing low-grade primary infection. Vaccinated mice developed significant delayed hypersensitivity reactions to soluble schistosome antigens in vivo. Splenocytes from vaccinated animals responded to in vitro culture with various specific antigens (soluble adult worm extract, living or disrupted schistosomula) by proliferation and production of macrophage-activating lymphokines as did lymphocytes from S. mansoni-infected animals. Macrophage-activating factors produced by spleen cells from vaccinated mice upon specific antigen stimulation eluted as a single peak on Sephadex G-100 with a molecular weight of approximately 50,000 and contained gamma interferon activity. Moreover, peritoneal macrophages with larvicidal and tumoricidal activity were recovered from vaccinated mice after intraperitoneal challenge with soluble schistosome antigens, a procedure also observed to elicit activated macrophages in S. mansoni-infected animals. These observations demonstrate that vaccination with irradiated cercariae stimulates many of the same cellular responses observed after primary S. mansoni infection, and suggest that lymphokine-activated macrophages may participate in the effector mechanism of vaccine-induced and concomitant immunity to challenge schistosome infection. This is the first demonstration of a potential immune effector mechanism in the irradiated vaccine model.
机译:在小鼠中比较了促成巨噬细胞活化的细胞介导的免疫反应,这些小鼠表现出对曼氏血吸虫感染的部分抵抗,这是由于接种了辐射减弱的尾c疫苗或正在进行的低度原发感染所致。接种疫苗的小鼠在体内对可溶性血吸虫抗原产生了明显的迟发型超敏反应。接种过疫苗的动物的脾细胞对体外培养的各种特异性抗原(可溶性成虫提取物,活的或破坏的血吸虫)通过巨噬细胞活化淋巴因子的增殖和产生作出反应,而曼氏感染曼氏感染的动物的淋巴细胞也是如此。在特异性抗原刺激下,由接种小鼠的脾细胞产生的巨噬细胞活化因子在Sephadex G-100上以单个峰的形式洗脱,分子量约为50,000,并具有γ干扰素活性。而且,在腹腔内用可溶性血吸虫抗原攻击后,从接种过的小鼠中回收了具有杀幼虫和杀虫活性的腹膜巨噬细胞,该方法还被观察到在曼氏沙门氏菌感染的动物中引起活化的巨噬细胞。这些观察结果表明,辐射的尾cer疫苗接种可刺激许多原发性曼氏沙门氏菌感染后观察到的相同细胞反应,并表明淋巴因子激活的巨噬细胞可能参与了疫苗诱导的并伴随的免疫反应,以挑战血吸虫病。这是辐射疫苗模型中潜在的免疫效应机制的首次证明。

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