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对呼吸道合胞病毒实验性诱导感染的免疫反应:在肺部疾病发展中的可能作用。

Immune response to experimentally induced infection with respiratory syncytial virus: possible role in the development of pulmonary disease.

作者信息

Piedra P A, Camussi G, Ogra P L

机构信息

Department of Pediatrics, State University of New York, Buffalo.

出版信息

J Gen Virol. 1989 Feb;70 ( Pt 2):325-33. doi: 10.1099/0022-1317-70-2-325.

DOI:10.1099/0022-1317-70-2-325
PMID:2732693
Abstract

Groups of mice were immunized intraperitoneally with HEp-2 lysate or respiratory syncytial virus (RSV)-infected HEp-2 cells with or without adjuvant(s). The animals were subsequently challenged intranasally (i.n.) with RSV and/or HEp-2 lysate and studied for RSV shedding in the lung, antigen-specific antibody response and pulmonary histopathology. A significant decrease in virus shedding was detected in each of four groups of animals immunized with a virus preparation and in two of four groups that received a HEp-2 lysate. Mice immunized with adjuvant(s) developed higher antibody-specific responses. All vaccinated animals developed pulmonary histopathology only on subsequent i.n. inoculation with RSV and/or HEp-2 lysate. Denatured extracts of purified RSV, HEp-2, BALB/c lung, cotton rat lung, Buffalo green monkey kidney and human buccal epithelium were tested for reactivity against the sera of immunized mice by an immunoblot method. Sera from all groups of immunized mice reacted with the extracts tested. The data suggest a possible role of reactivity to viral as well as non-viral components in the pathogenesis of RSV vaccine-induced pulmonary inflammation in the mouse model system.

摘要

将小鼠分组,用HEp-2裂解物或呼吸道合胞病毒(RSV)感染的HEp-2细胞腹腔内免疫,添加或不添加佐剂。随后,给动物经鼻内(i.n.)接种RSV和/或HEp-2裂解物,并研究肺内RSV脱落情况、抗原特异性抗体反应和肺组织病理学。在用病毒制剂免疫的四组动物中的每组以及接受HEp-2裂解物的四组中的两组中,均检测到病毒脱落显著减少。用佐剂免疫的小鼠产生了更高的抗体特异性反应。所有接种疫苗的动物仅在随后经鼻内接种RSV和/或HEp-2裂解物时才出现肺组织病理学变化。通过免疫印迹法检测纯化的RSV、HEp-2、BALB/c肺、棉鼠肺、水牛绿猴肾和人颊黏膜上皮的变性提取物与免疫小鼠血清的反应性。所有免疫小鼠组的血清均与所测试的提取物发生反应。数据表明,在小鼠模型系统中,对病毒和非病毒成分的反应性在RSV疫苗诱导的肺部炎症发病机制中可能起作用。

相似文献

1
Immune response to experimentally induced infection with respiratory syncytial virus: possible role in the development of pulmonary disease.对呼吸道合胞病毒实验性诱导感染的免疫反应:在肺部疾病发展中的可能作用。
J Gen Virol. 1989 Feb;70 ( Pt 2):325-33. doi: 10.1099/0022-1317-70-2-325.
2
Cotton rats previously immunized with a chimeric RSV FG glycoprotein develop enhanced pulmonary pathology when infected with RSV, a phenomenon not encountered following immunization with vaccinia--RSV recombinants or RSV.先前用嵌合呼吸道合胞病毒(RSV)融合糖蛋白免疫的棉鼠,在感染RSV时会出现肺部病理变化加重的情况,而在用痘苗-RSV重组体或RSV免疫后则不会出现这种现象。
Vaccine. 1992;10(7):475-84. doi: 10.1016/0264-410x(92)90397-3.
3
Pulmonary histopathology induced by respiratory syncytial virus (RSV) challenge of formalin-inactivated RSV-immunized BALB/c mice is abrogated by depletion of CD4+ T cells.用甲醛灭活的呼吸道合胞病毒(RSV)免疫BALB/c小鼠,然后对其进行RSV攻击所诱导的肺部组织病理学变化,可通过清除CD4+ T细胞而消除。
J Virol. 1992 Dec;66(12):7444-51. doi: 10.1128/JVI.66.12.7444-7451.1992.
4
Mechanism of lung injury in cotton rats immunized with formalin-inactivated respiratory syncytial virus.用福尔马林灭活呼吸道合胞病毒免疫的棉鼠肺损伤机制。
Vaccine. 1989 Feb;7(1):34-8. doi: 10.1016/0264-410x(89)90008-x.
5
Enhanced pulmonary histopathology is observed in cotton rats immunized with formalin-inactivated respiratory syncytial virus (RSV) or purified F glycoprotein and challenged with RSV 3-6 months after immunization.在用福尔马林灭活的呼吸道合胞病毒(RSV)或纯化的F糖蛋白免疫并在免疫后3 - 6个月用RSV攻击的棉鼠中,观察到肺部组织病理学增强。
Vaccine. 1990 Oct;8(5):497-502. doi: 10.1016/0264-410x(90)90253-i.
6
Detection of respiratory syncytial virus (RSV) infected cells by in situ hybridization in the lungs of cotton rats immunized with formalin-inactivated virus or purified RSV F and G glycoprotein subunit vaccine and challenged with RSV.在用福尔马林灭活病毒或纯化的呼吸道合胞病毒(RSV)F和G糖蛋白亚单位疫苗免疫并用RSV攻击的棉鼠肺中,通过原位杂交检测RSV感染的细胞。
Virus Res. 1990 Jun;16(2):153-62. doi: 10.1016/0168-1702(90)90019-8.
7
A human respiratory syncytial virus (RSV) primate model of enhanced pulmonary pathology induced with a formalin-inactivated RSV vaccine but not a recombinant FG subunit vaccine.一种人类呼吸道合胞病毒(RSV)灵长类动物模型,该模型显示用福尔马林灭活的RSV疫苗而非重组FG亚基疫苗可诱导肺部病理增强。
J Infect Dis. 1993 Mar;167(3):553-61. doi: 10.1093/infdis/167.3.553.
8
Influenza virus vaccine expressing fusion and attachment protein epitopes of respiratory syncytial virus induces protective antibodies in BALB/c mice.表达呼吸道合胞病毒融合和附着蛋白表位的流感病毒疫苗可在BALB/c小鼠中诱导产生保护性抗体。
Antiviral Res. 2014 Apr;104:110-7. doi: 10.1016/j.antiviral.2014.01.022. Epub 2014 Feb 6.
9
Comparison of the ability of formalin-inactivated respiratory syncytial virus, immunopurified F, G and N proteins and cell lysate to enhance pulmonary changes in Balb/c mice.甲醛灭活呼吸道合胞病毒、免疫纯化的F、G和N蛋白以及细胞裂解物增强Balb/c小鼠肺部病变能力的比较。
Vaccine. 1992;10(2):113-8. doi: 10.1016/0264-410x(92)90027-h.
10
Plasmid DNA encoding the respiratory syncytial virus G protein is a promising vaccine candidate.编码呼吸道合胞病毒G蛋白的质粒DNA是一种很有前景的候选疫苗。
Virology. 2000 Mar 30;269(1):54-65. doi: 10.1006/viro.2000.0186.

引用本文的文献

1
Preclinical evaluation of bacterially produced RSV-G protein vaccine: Strong protection against RSV challenge in cotton rat model.细菌表达的 RSV-G 蛋白疫苗的临床前评价:在棉鼠模型中对 RSV 挑战具有强大的保护作用。
Sci Rep. 2017 Feb 10;7:42428. doi: 10.1038/srep42428.
2
Antioxidant treatment ameliorates respiratory syncytial virus-induced disease and lung inflammation.抗氧化剂治疗可改善呼吸道合胞病毒引起的疾病和肺部炎症。
Am J Respir Crit Care Med. 2006 Dec 15;174(12):1361-9. doi: 10.1164/rccm.200603-319OC. Epub 2006 Sep 28.