Nappi A J, Vass E, Malagoli D, Carton Y
Department of Animal Health and Biomedical Sciences, University of Wisconsin, Madison, Wisconsin 53706, USA.
J Parasitol. 2004 Oct;90(5):1139-49. doi: 10.1645/GE-266R.
Immune-suppressive factors (ISFs) introduced into larvae of Drosophila melanogaster during infection by virulent endoparasitic wasps effectively block the innate immune response mediated by blood cells (hemocytes) but have little influence on the autoimmune response made by a tumor strain in which the blood cells manifest a similar response but instead target and destroy endogenous tissues. Quantitative hemocyte analyses indicate that ISFs interfere with the immune effector responses downstream of nonself recognition, hemocyte activation and differentiation, because these responses were manifested by tumor hosts, in which the parasitoids developed. The data suggest that once activated to encapsulate aberrant tissues, the target specificity of the autoimmune-activated hemocytes, and the genetic program underlying tumor formation, cannot be blocked by parasitoid-derived ISFs, which effectively inhibit identical hemocyte-mediated responses during parasitization.
在感染毒性内寄生蜂期间引入黑腹果蝇幼虫体内的免疫抑制因子(ISFs)可有效阻断血细胞介导的先天免疫反应,但对一种肿瘤品系的自身免疫反应影响甚微,在该肿瘤品系中血细胞表现出类似反应,但却靶向并破坏内源性组织。血细胞定量分析表明,ISFs干扰非自身识别、血细胞激活和分化下游的免疫效应反应,因为这些反应在寄生蜂发育的肿瘤宿主中表现出来。数据表明,一旦被激活以包裹异常组织,自身免疫激活的血细胞的靶标特异性以及肿瘤形成的遗传程序,不能被寄生蜂衍生的ISFs阻断,而这些ISFs在寄生过程中可有效抑制相同的血细胞介导的反应。