Bradford H E, Adair B M, McNulty M S, Foster J C
Veterinary Research Laboratories, Stormont, Belfast, UK.
Vet Immunol Immunopathol. 1992 Feb 15;31(1-2):115-27. doi: 10.1016/0165-2427(92)90090-d.
The cytotoxic effect of bovine neutrophils, alveolar macrophages, monocytes and lymphocytes for parainfluenza type-3 (PI-3) virus-infected cells in 51chromium-release assays is described. Specific lysis of virus-infected target cells with PI-3 virus antibody and complement was first observed 8 h after infection coincident with the appearance of haemadsorption-positive cells. Specific lysis increased rapidly reaching a peak 18-24 h after infection. This increase was paralleled by the increase in the percentage of cells with surface haemagglutinin. Target cells were subsequently used in 51chromium-release assays between 18 and 20 h after virus infection. Antibody-independent killing of PI-3 virus-infected cells was observed with neutrophils, alveolar macrophages and lymphocytes. Levels of specific lysis up to 30% for neutrophils and 68% for alveolar macrophages were observed, although there was considerable variation in activity from animal to animal. Lymphocyte preparations showed levels of cytotoxicity up to 20% in some cases while monocytes had low killing ability. Addition of PI-3 virus-specific antibodies enhanced killing by neutrophils, monocytes and lymphocytes but inhibited killing by alveolar macrophages. Complement, particularly guinea pig complement, was cytotoxic for virus-infected but not for uninfected cells, and also considerably enhanced the cytotoxic effect of neutrophils and lymphocytes.
本文描述了在51铬释放试验中,牛嗜中性粒细胞、肺泡巨噬细胞、单核细胞和淋巴细胞对3型副流感病毒(PI-3)感染细胞的细胞毒性作用。感染后8小时首次观察到用PI-3病毒抗体和补体对病毒感染靶细胞的特异性裂解,这与血细胞吸附阳性细胞的出现同时发生。特异性裂解迅速增加,在感染后18 - 24小时达到峰值。这种增加与表面血凝素阳性细胞百分比的增加平行。随后在病毒感染后18至20小时使用靶细胞进行51铬释放试验。观察到嗜中性粒细胞、肺泡巨噬细胞和淋巴细胞对PI-3病毒感染细胞有抗体非依赖性杀伤作用。观察到嗜中性粒细胞的特异性裂解水平高达30%,肺泡巨噬细胞高达68%,尽管不同动物之间的活性存在相当大的差异。淋巴细胞制剂在某些情况下显示出高达20%的细胞毒性水平,而单核细胞的杀伤能力较低。添加PI-3病毒特异性抗体可增强嗜中性粒细胞、单核细胞和淋巴细胞的杀伤作用,但抑制肺泡巨噬细胞的杀伤作用。补体,特别是豚鼠补体,对病毒感染细胞具有细胞毒性,但对未感染细胞无细胞毒性,并且还显著增强了嗜中性粒细胞和淋巴细胞的细胞毒性作用。