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塞姆利基森林病毒诱导的免疫介导性脱髓鞘:辐射的影响

Semliki Forest virus induced, immune mediated demyelination: the effect of irradiation.

作者信息

Fazakerley J K, Webb H E

出版信息

Br J Exp Pathol. 1987 Feb;68(1):101-13.

Abstract

Intraperitoneal infection with the avirulent A7(74) strain of the alphavirus Semliki Forest virus (SFV) induces an immune mediated demyelinating encephalomyelitis. The blood and brain virus titres, the serum antibody titres and the histopathological changes in the brains of normal mice and mice immunosuppressed with 5.0 or 8.0 Gy total body irradiation (TBX) were determined. SFV infection of immunosuppressed mice resulted in persistently high blood and brain virus titres, neuronal pycnosis, paralysis and death. No demyelination or central nervous system (CNS) inflammatory response occurred in these immunosuppressed mice despite high and persistent brain virus titres. The CNS inflammatory response and associated demyelination could be restored to infected immunosuppressed mice by adoptive transfer of spleen cells, and these changes were brought forward if the donor spleen cells were from mice previously sensitized to SFV. The results indicate that the immune response following SFV A7(74) infection is both protective and pathogenic, and that the demyelination is immune mediated and does not result from direct viral destruction of oligodendrocytes, or any other direct effect of the virus.

摘要

用无致病性的甲病毒塞姆利基森林病毒(SFV)的A7(74)毒株进行腹腔感染可诱发免疫介导的脱髓鞘性脑脊髓炎。测定了正常小鼠以及经5.0或8.0 Gy全身照射(TBX)免疫抑制的小鼠的血液和脑病毒滴度、血清抗体滴度以及脑内的组织病理学变化。免疫抑制小鼠感染SFV后,血液和脑病毒滴度持续居高不下,出现神经元固缩、麻痹和死亡。尽管脑病毒滴度高且持续存在,但这些免疫抑制小鼠未发生脱髓鞘或中枢神经系统(CNS)炎症反应。通过脾细胞的过继转移可使感染的免疫抑制小鼠恢复CNS炎症反应及相关的脱髓鞘,并且如果供体脾细胞来自先前对SFV致敏的小鼠,这些变化会提前出现。结果表明,SFV A7(74)感染后的免疫反应既有保护作用又有致病作用,并且脱髓鞘是由免疫介导的,并非由病毒对少突胶质细胞的直接破坏或病毒的任何其他直接作用所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa70/2012988/df277cf79849/brjexppathol00007-0102-a.jpg

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