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在免疫后3至6个月受到攻击时,用呼吸道合胞病毒(RSV)纯化F糖蛋白免疫的棉鼠未检测到肺部组织病理学增强。

Lack of detectable enhanced pulmonary histopathology in cotton rats immunized with purified F glycoprotein of respiratory syncytial virus (RSV) when challenged at 3-6 months after immunization.

作者信息

Hildreth S W, Baggs R R, Brownstein D G, Castleman W L, Paradiso P R

机构信息

Virology Research, Praxis Biologics, Rochester, NY 14623.

出版信息

Vaccine. 1993;11(6):615-8. doi: 10.1016/0264-410x(93)90304-g.

DOI:10.1016/0264-410x(93)90304-g
PMID:8322482
Abstract

The cotton rat model has been used to evaluate the potential for immunogens to induce respiratory syncytial virus (RSV)-enhanced pulmonary histopathology. A recent study evaluated purified F protein in this model when animals were challenged intranasally with RSV 3 or 6 months after immunization. The authors concluded that the purified F protein was associated with the same level of histopathological changes as observed with the positive control, a formalin-inactivated RSV immunogen. Three pathologists have independently evaluated the lung sections from the animals of this study and the results are reported in this article. In contrast to the previously published data, we have found that F protein was associated with a substantially milder and qualitatively different response to that observed with the formalin-inactivated RSV vaccine. We concluded that the minimal histological changes observed and lack of clinical disease make it very difficult to assess the issue of enhanced pulmonary RSV disease with the cotton rat model.

摘要

棉鼠模型已被用于评估免疫原诱导呼吸道合胞病毒(RSV)增强型肺部组织病理学的可能性。最近一项研究在该模型中评估了纯化的F蛋白,免疫动物在免疫后3或6个月经鼻用RSV攻击。作者得出结论,纯化的F蛋白与阳性对照(福尔马林灭活的RSV免疫原)所观察到的组织病理学变化水平相同。三位病理学家独立评估了本研究动物的肺切片,结果报告于本文。与先前发表的数据相反,我们发现F蛋白所引发的反应比福尔马林灭活的RSV疫苗所观察到的反应明显更轻且性质不同。我们得出结论,观察到的最小组织学变化以及缺乏临床疾病使得用棉鼠模型评估RSV增强型肺部疾病问题非常困难。

相似文献

1
Lack of detectable enhanced pulmonary histopathology in cotton rats immunized with purified F glycoprotein of respiratory syncytial virus (RSV) when challenged at 3-6 months after immunization.在免疫后3至6个月受到攻击时,用呼吸道合胞病毒(RSV)纯化F糖蛋白免疫的棉鼠未检测到肺部组织病理学增强。
Vaccine. 1993;11(6):615-8. doi: 10.1016/0264-410x(93)90304-g.
2
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.
3
Immunogen-induced enhanced pulmonary histopathology in the RSV cotton rat model.
Vaccine. 1993;11(6):689-90. doi: 10.1016/0264-410x(93)90328-u.
4
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.
5
Immunization of cotton rats with the fusion (F) and large (G) glycoproteins of respiratory syncytial virus (RSV) protects against RSV challenge without potentiating RSV disease.用呼吸道合胞病毒(RSV)的融合(F)糖蛋白和大(G)糖蛋白对棉鼠进行免疫接种,可预防RSV攻击,且不会加重RSV疾病。
Vaccine. 1989 Dec;7(6):533-40. doi: 10.1016/0264-410x(89)90278-8.
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
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.
8
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.
9
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.
10
Vaccination of cotton rats with a chimeric FG glycoprotein of human respiratory syncytial virus induces minimal pulmonary pathology on challenge.
J Infect Dis. 1991 Mar;163(3):477-82. doi: 10.1093/infdis/163.3.477.

引用本文的文献

1
A randomized controlled trial comparing non-steroidal anti-inflammatory and fusion protein inhibitors singly and in combination on the histopathology of bovine respiratory syncytial virus infection.一项比较非甾体抗炎药和融合蛋白抑制剂单独及联合应用对牛呼吸道合胞体病毒感染组织病理学影响的随机对照试验。
PLoS One. 2021 Jun 10;16(6):e0252455. doi: 10.1371/journal.pone.0252455. eCollection 2021.
2
Disruption of the CD40-CD40 ligand system prevents an oxygen-induced respiratory distress syndrome.CD40-CD40配体系统的破坏可预防氧诱导的呼吸窘迫综合征。
Am J Pathol. 1998 Mar;152(3):651-7.
3
Respiratory synctial virus infection in BALB/c mice previously immunized with formalin-inactivated virus induces enhanced pulmonary inflammatory response with a predominant Th2-like cytokine pattern.
用福尔马林灭活病毒预先免疫的BALB/c小鼠感染呼吸道合胞病毒后,会诱导出以Th2样细胞因子模式为主的增强型肺部炎症反应。
J Virol. 1996 May;70(5):2852-60. doi: 10.1128/JVI.70.5.2852-2860.1996.