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抗H5N1流感人源单克隆抗体的预防和治疗效果

Prophylactic and therapeutic efficacy of human monoclonal antibodies against H5N1 influenza.

作者信息

Simmons Cameron P, Bernasconi Nadia L, Suguitan Amorsolo L, Mills Kimberly, Ward Jerrold M, Chau Nguyen Van Vinh, Hien Tran Tinh, Sallusto Federica, Ha Do Quang, Farrar Jeremy, de Jong Menno D, Lanzavecchia Antonio, Subbarao Kanta

机构信息

Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.

出版信息

PLoS Med. 2007 May;4(5):e178. doi: 10.1371/journal.pmed.0040178.

Abstract

BACKGROUND

New prophylactic and therapeutic strategies to combat human infections with highly pathogenic avian influenza (HPAI) H5N1 viruses are needed. We generated neutralizing anti-H5N1 human monoclonal antibodies (mAbs) and tested their efficacy for prophylaxis and therapy in a murine model of infection.

METHODS AND FINDINGS

Using Epstein-Barr virus we immortalized memory B cells from Vietnamese adults who had recovered from infections with HPAI H5N1 viruses. Supernatants from B cell lines were screened in a virus neutralization assay. B cell lines secreting neutralizing antibodies were cloned and the mAbs purified. The cross-reactivity of these antibodies for different strains of H5N1 was tested in vitro by neutralization assays, and their prophylactic and therapeutic efficacy in vivo was tested in mice. In vitro, mAbs FLA3.14 and FLD20.19 neutralized both Clade I and Clade II H5N1 viruses, whilst FLA5.10 and FLD21.140 neutralized Clade I viruses only. In vivo, FLA3.14 and FLA5.10 conferred protection from lethality in mice challenged with A/Vietnam/1203/04 (H5N1) in a dose-dependent manner. mAb prophylaxis provided a statistically significant reduction in pulmonary virus titer, reduced associated inflammation in the lungs, and restricted extrapulmonary dissemination of the virus. Therapeutic doses of FLA3.14, FLA5.10, FLD20.19, and FLD21.140 provided robust protection from lethality at least up to 72 h postinfection with A/Vietnam/1203/04 (H5N1). mAbs FLA3.14, FLD21.140 and FLD20.19, but not FLA5.10, were also therapeutically active in vivo against the Clade II virus A/Indonesia/5/2005 (H5N1).

CONCLUSIONS

These studies provide proof of concept that fully human mAbs with neutralizing activity can be rapidly generated from the peripheral blood of convalescent patients and that these mAbs are effective for the prevention and treatment of H5N1 infection in a mouse model. A panel of neutralizing, cross-reactive mAbs might be useful for prophylaxis or adjunctive treatment of human cases of H5N1 influenza.

摘要

背景

需要新的预防和治疗策略来对抗人类感染高致病性禽流感(HPAI)H5N1病毒。我们制备了中和性抗H5N1人单克隆抗体(mAb),并在小鼠感染模型中测试了它们的预防和治疗效果。

方法与结果

利用爱泼斯坦-巴尔病毒使从感染HPAI H5N1病毒后康复的越南成年人的记忆B细胞永生化。在病毒中和试验中筛选B细胞系的上清液。克隆分泌中和抗体的B细胞系并纯化mAb。通过中和试验在体外测试这些抗体对不同H5N1毒株的交叉反应性,并在小鼠体内测试它们的预防和治疗效果。在体外,mAb FLA3.14和FLD20.19中和了第I分支和第II分支的H5N1病毒,而FLA5.10和FLD21.140仅中和第I分支病毒。在体内,FLA3.1和FLA5.10以剂量依赖的方式使感染A/越南/1203/04(H5N1)的小鼠免于死亡。mAb预防在统计学上显著降低了肺部病毒滴度,减轻了肺部相关炎症,并限制了病毒的肺外扩散。治疗剂量的FLA3.14、FLA5.10、FLD20.19和FLD21.140至少在感染A/越南/1203/04(H5N1)后72小时内提供了强大的免于死亡的保护。mAb FLA3.14、FLD21.140和FLD20.1但不是FLA5.10在体内对第II分支病毒A/印度尼西亚/5/2005(H5N1)也具有治疗活性。

结论

这些研究提供了概念验证,即可以从康复患者的外周血中快速产生具有中和活性的完全人源mAb,并且这些mAb在小鼠模型中对H5N1感染的预防和治疗有效。一组中和性、交叉反应性mAb可能对人类H5N1流感病例的预防或辅助治疗有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030f/1880850/7d9a827258f3/pmed.0040178.g001.jpg

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