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Immunocyte Response to Experimental Mumps Virus Infection in Rhesus Monkeys

机译:免疫细胞对恒河猴实验性腮腺炎病毒感染的反应

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Nineteen rhesus monkeys were inoculated with mumps virus by retrograde ductal instillation into the parotid gland. Evidence of infection was obtained in all instances. Virus was isolated from buccal swabbings and parotid biopsies for 1 week after inoculation. A vigorous serum-neutralizing antibody response occurred within 3 weeks, and there was marked monocytic infiltration of the parotid stroma. The monocytic infiltrate comprised as much as 60% of the total gland volume 1 week after infection. The predominant inflammatory cells were non-immunoglobulin-containing mononuclear cells resembling lymphocytes. Plasma cells containing immunoglobulin G (IgG), IgA, IgM, and IgE increased in numbers in the gland after infection, the greatest increase occurring in IgG-containing cells. Neutralizing antibodies and interferon were found in extracts prepared from the infected glands. Neutralizing activity was highest in samples taken 3 weeks after infection but was detectable in samples taken as soon as 36 to 48 h after infection. Interferon activity was detected in significant amounts 36 to 48 h after infection. Challenge of previously infected animals resulted in an increase in the monocytic infiltrate as well as an increase in numbers of immunoglobulin-containing plasma cells. However, reinfection did not occur as evidenced by the inability to culture shed virus after challenge. This model should be useful for in vivo study of biochemical mediators which evoke inflammatory cell infiltration and which may be significant both in protection and in tissue damage.
机译:通过逆行导管滴入腮腺向19只恒河猴接种腮腺炎病毒。在所有情况下均获得了感染证据。接种1周后,从颊拭子和腮腺活检组织中分离出病毒。在3周内发生了强烈的血清中和抗体反应,并且腮腺基质明显浸润了单核细胞。感染后1周,单核细胞浸润占总腺体体积的60%。主要的炎性细胞是类似淋巴细胞的非免疫球蛋白单核细胞。感染后,含有免疫球蛋白G(IgG),IgA,IgM和IgE的浆细胞在腺体中数量增加,最大的增加发生在含IgG的细胞中。在从感染腺体制备的提取物中发现了中和抗体和干扰素。感染后3周采集的样品中和活性最高,但感染后36至48 h即可检测到中和活性。感染后36至48小时内检测到大量干扰素活性。先前感染动物的攻击导致单核细胞浸润的增加以及含免疫球蛋白的浆细胞数量的增加。然而,如在攻击后不能培养脱落病毒所证明的那样,没有发生再感染。该模型应可用于体内研究引起炎症细胞浸润的生化介质,并且在保护和组织损伤方面均可能具有重要意义。

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