Kjellén L, Ankerst J
J Virol. 1973 Jul;12(1):25-32. doi: 10.1128/JVI.12.1.25-32.1973.
Adenovirus-antibody aggregates under defined conditions are cytotoxic in vitro. All members of adenovirus groups I, II, and III caused toxicity upon aggregation. The toxicity of the clusters is exerted by the virions. Toxicity is temperature dependent and may be caused by a mechanism similar to that used in viral penetration. Cells permitting direct viral penetration were all sensitive to the toxic aggregates. The toxicity seems to be related to hexon antigens on the surface of the virions since antihexon sera neutralized the toxicity. No evidence was obtained showing that pentons are required for this kind of cytotoxicity. Adenovirus types 3, 5, and 9 were used in the experiment. Cytotoxicity was estimated by the (51)Cr release assay. Complement factors could be excluded as mediators of the cytolytic reactions. Instead, complement was shown to prevent the formation of toxic aggregates or to neutralize the toxicity of preformed ones.
在特定条件下,腺病毒 - 抗体聚集体在体外具有细胞毒性。腺病毒Ⅰ、Ⅱ和Ⅲ组的所有成员在聚集时都会产生毒性。聚集体的毒性由病毒粒子发挥作用。毒性取决于温度,其产生机制可能与病毒穿透所使用的机制类似。允许病毒直接穿透的细胞对毒性聚集体均敏感。毒性似乎与病毒粒子表面的六邻体抗原有关,因为抗六邻体血清可中和毒性。没有证据表明这种细胞毒性需要五邻体。实验中使用了3型、5型和9型腺病毒。细胞毒性通过(51)Cr释放试验进行评估。补体因子可被排除作为溶细胞反应的介质。相反,补体被证明可阻止毒性聚集体的形成或中和预先形成的聚集体的毒性。