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J Exp Med. 1988 Sep 1;168(3):1163-8. doi: 10.1084/jem.168.3.1163.
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Exposure to bacterial PAMPs before RSV infection exacerbates innate inflammation and disease via IL-1α and TNF-α.在呼吸道合胞病毒(RSV)感染前暴露于细菌病原体相关分子模式(PAMPs)会通过白细胞介素-1α(IL-1α)和肿瘤坏死因子-α(TNF-α)加剧先天性炎症和疾病。
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Human T cells efficiently control RSV infection.人体 T 细胞能有效地控制 RSV 感染。
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本文引用的文献

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Recovery from a viral respiratory infection. I. Influenza pneumonia in normal and T-deficient mice.从病毒性呼吸道感染中恢复。I. 正常小鼠和T细胞缺陷小鼠的流感肺炎
J Immunol. 1981 Mar;126(3):1036-41.
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Respiratory syncytial virus infection in mice.小鼠呼吸道合胞病毒感染
Infect Immun. 1984 Feb;43(2):649-55. doi: 10.1128/iai.43.2.649-655.1984.
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Defective regulation of immune responses in respiratory syncytial virus infection.呼吸道合胞病毒感染中免疫反应的调节缺陷。
J Immunol. 1984 Oct;133(4):1925-30.
4
Monoclonal antibodies protect against respiratory syncytial virus infection in mice.单克隆抗体可保护小鼠免受呼吸道合胞病毒感染。
Immunology. 1984 May;52(1):137-42.
5
Respiratory syncytial virus. Brief review.呼吸道合胞病毒。简要综述。
Arch Virol. 1985;84(1-2):1-52. doi: 10.1007/BF01310552.
6
Effectiveness of topically administered neutralizing antibodies in experimental immunotherapy of respiratory syncytial virus infection in cotton rats.局部给予中和抗体在棉鼠呼吸道合胞病毒感染实验性免疫治疗中的有效性。
J Virol. 1987 Jun;61(6):1851-4. doi: 10.1128/JVI.61.6.1851-1854.1987.
7
Clearance of persistent respiratory syncytial virus infections in immunodeficient mice following transfer of primed T cells.在输注经致敏的T细胞后免疫缺陷小鼠体内持续性呼吸道合胞病毒感染的清除
Immunology. 1987 Sep;62(1):133-8.
8
Cytotoxic T cell specificity for respiratory syncytial virus proteins: fusion protein is an important target antigen.细胞毒性T细胞对呼吸道合胞病毒蛋白的特异性:融合蛋白是重要的靶抗原。
J Gen Virol. 1987 Aug;68 ( Pt 8):2177-82. doi: 10.1099/0022-1317-68-8-2177.
9
Immune and histopathological responses in animals vaccinated with recombinant vaccinia viruses that express individual genes of human respiratory syncytial virus.用表达人呼吸道合胞病毒单个基因的重组痘苗病毒接种的动物的免疫和组织病理学反应。
J Virol. 1987 Dec;61(12):3855-61. doi: 10.1128/JVI.61.12.3855-3861.1987.
10
Microplaque immunoperoxidase detection of infectious respiratory syncytial virus in the lungs of infected mice.微斑免疫过氧化物酶法检测感染小鼠肺内的传染性呼吸道合胞病毒
J Virol Methods. 1987 Jul;16(4):293-301. doi: 10.1016/0166-0934(87)90014-0.

细胞毒性T细胞可清除病毒,但会加剧感染呼吸道合胞病毒小鼠的肺部病变。

Cytotoxic T cells clear virus but augment lung pathology in mice infected with respiratory syncytial virus.

作者信息

Cannon M J, Openshaw P J, Askonas B A

机构信息

Division of Immunology, National Institute for Medical Research, London, United Kingdom.

出版信息

J Exp Med. 1988 Sep 1;168(3):1163-8. doi: 10.1084/jem.168.3.1163.

DOI:10.1084/jem.168.3.1163
PMID:3262705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2189034/
Abstract

We have examined the function of class I MHC-restricted cytotoxic T cells in experimental respiratory syncytial virus (RSV) infection of BALB/c mice by transfer of T cell line MJC-A2 and CTL clone E8a into RSV-infected mice. The T cell line cleared pulmonary RSV infection within 5 d in persistently infected gamma-irradiated mice, but caused acute respiratory disease. This was only seen in infected mice and was often lethal after transfer of greater than 3 x 10(6) CTL. Lower numbers of CTL produced less severe disease but still cleared lung RSV, albeit over a longer time course (up to 10 d). Clearance of lung RSV in immunocompetent mice by the T cell line and CTL clone was again accompanied by acute and sometimes lethal respiratory disease. Bronchoalveolar lavage showed severe lung hemorrhage and frequent neutrophil efflux in mice with CTL-augmented disease.

摘要

我们通过将T细胞系MJC - A2和CTL克隆E8a转移到呼吸道合胞病毒(RSV)感染的BALB/c小鼠体内,研究了I类主要组织相容性复合体(MHC)限制性细胞毒性T细胞在实验性RSV感染中的作用。该T细胞系在持续感染的经γ射线照射的小鼠中,于5天内清除了肺部的RSV感染,但引发了急性呼吸道疾病。这种情况仅在感染小鼠中出现,且在转移超过3×10⁶个CTL后通常是致命的。较低数量的CTL产生的疾病较轻,但仍能清除肺部的RSV,尽管所需时间更长(长达10天)。T细胞系和CTL克隆在免疫活性小鼠中清除肺部RSV的同时,再次伴有急性且有时致命的呼吸道疾病。支气管肺泡灌洗显示,在CTL增强疾病的小鼠中存在严重的肺出血和频繁的中性粒细胞外流。