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呼吸道合胞病毒的22000千道尔顿蛋白是受感染引发的小鼠中Kd限制细胞毒性T淋巴细胞的主要靶点。

The 22,000-kilodalton protein of respiratory syncytial virus is a major target for Kd-restricted cytotoxic T lymphocytes from mice primed by infection.

作者信息

Openshaw P J, Anderson K, Wertz G W, Askonas B A

机构信息

National Institute for Medical Research, Mill Hill, London, United Kingdom.

出版信息

J Virol. 1990 Apr;64(4):1683-9. doi: 10.1128/JVI.64.4.1683-1689.1990.

Abstract

Recombinant vaccinia viruses containing the 22-kilodalton protein (matrixlike or 22K protein) or phosphoprotein gene from respiratory syncytial virus were constructed. These recombinant viruses expressed proteins which were immunoprecipitated by appropriate respiratory syncytial virus antibodies and comigrated with authentic proteins produced by respiratory syncytial virus infection. The new recombinant viruses (and others previously described containing the attachment glycoprotein, fusion, or nucleoprotein genes of respiratory syncytial virus) were used to infect target cells for cultured polyclonal cytotoxic T lymphocytes generated from the spleens of BALB/c or DBA/2 mice primed by intranasal infection with respiratory syncytial virus. Respiratory syncytial virus-specific cytotoxic T lymphocytes (CTL) showed strong Kd (but not Dd)-restricted recognition of the 22K protein. As previously reported, the fusion protein and nucleoprotein were both seen by CTL, but recognition of these proteins was comparatively weak. There was no detectable recognition of other respiratory syncytial virus proteins tested (including phosphoprotein). 22K protein-specific splenic memory CTL persisted for at least 11 months after infection of BALB/c mice. Priming BALB/c mice with recombinant vaccinia virus containing the 22K protein gene induced respiratory syncytial virus-specific memory CTL at lower levels than that previously reported following infection with a similar recombinant containing the fusion protein gene. These data identify the 22K protein as a major target antigen for respiratory syncytial virus-specific CTL from H-2d mice primed by respiratory syncytial virus infection.

摘要

构建了含有呼吸道合胞病毒22千道尔顿蛋白(基质样或22K蛋白)或磷蛋白基因的重组痘苗病毒。这些重组病毒表达的蛋白能被合适的呼吸道合胞病毒抗体免疫沉淀,并与呼吸道合胞病毒感染产生的天然蛋白迁移率相同。新的重组病毒(以及先前描述的含有呼吸道合胞病毒附着糖蛋白、融合蛋白或核蛋白基因的其他重组病毒)被用于感染由经鼻感染呼吸道合胞病毒致敏的BALB/c或DBA/2小鼠脾脏产生的培养多克隆细胞毒性T淋巴细胞的靶细胞。呼吸道合胞病毒特异性细胞毒性T淋巴细胞(CTL)对22K蛋白表现出强烈的Kd(而非Dd)限制性识别。如先前报道,CTL能识别融合蛋白和核蛋白,但对这些蛋白的识别相对较弱。未检测到对所测试的其他呼吸道合胞病毒蛋白(包括磷蛋白)的识别。在感染BALB/c小鼠后,22K蛋白特异性脾脏记忆CTL持续存在至少11个月。用含有22K蛋白基因的重组痘苗病毒免疫BALB/c小鼠,诱导产生的呼吸道合胞病毒特异性记忆CTL水平低于先前报道的用含有融合蛋白基因的类似重组病毒感染后产生的水平。这些数据表明,22K蛋白是经呼吸道合胞病毒感染致敏的H-2d小鼠中呼吸道合胞病毒特异性CTL的主要靶抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1433/249305/e6a7c259896c/jvirol00059-0277-a.jpg

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