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Multimechanistic Monoclonal Antibodies (MAbs) Targeting Staphylococcus aureus Alpha-Toxin and Clumping Factor A: Activity and Efficacy Comparisons of a MAb Combination and an Engineered Bispecific Antibody Approach.多机制单克隆抗体(MAbs)靶向金黄色葡萄球菌α-毒素和聚集因子 A:单克隆抗体组合和工程双特异性抗体方法的活性和疗效比较。
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本文引用的文献

1
IVIG-mediated protection against necrotizing pneumonia caused by MRSA.静脉注射免疫球蛋白对耐甲氧西林金黄色葡萄球菌导致的坏死性肺炎的保护作用。
Sci Transl Med. 2016 Sep 21;8(357):357ra124. doi: 10.1126/scitranslmed.aag1153.
2
Improved Protection in a Rabbit Model of Community-Associated Methicillin-Resistant Staphylococcus aureus Necrotizing Pneumonia upon Neutralization of Leukocidins in Addition to Alpha-Hemolysin.在社区获得性耐甲氧西林金黄色葡萄球菌坏死性肺炎兔模型中,除α-溶血素外,中和杀白细胞素后保护作用增强。
Antimicrob Agents Chemother. 2016 Sep 23;60(10):6333-40. doi: 10.1128/AAC.01213-16. Print 2016 Oct.
3
Normalizing the environment recapitulates adult human immune traits in laboratory mice.使环境正常化可在实验室小鼠中重现成年人类的免疫特征。
Nature. 2016 Apr 28;532(7600):512-6. doi: 10.1038/nature17655. Epub 2016 Apr 20.
4
Staphylococcus aureus α toxin potentiates opportunistic bacterial lung infections.金黄色葡萄球菌α毒素会加重机会性细菌性肺部感染。
Sci Transl Med. 2016 Mar 9;8(329):329ra31. doi: 10.1126/scitranslmed.aad9922.
5
Antibacterial monoclonal antibodies: the next generation?抗菌单克隆抗体:下一代?
Curr Opin Microbiol. 2015 Oct;27:78-85. doi: 10.1016/j.mib.2015.07.014. Epub 2015 Aug 25.
6
MEDI4893* Promotes Survival and Extends the Antibiotic Treatment Window in a Staphylococcus aureus Immunocompromised Pneumonia Model.MEDI4893在金黄色葡萄球菌免疫受损肺炎模型中促进存活并延长抗生素治疗窗口。
Antimicrob Agents Chemother. 2015 Aug;59(8):4526-32. doi: 10.1128/AAC.00510-15. Epub 2015 May 18.
7
Five birds, one stone: neutralization of α-hemolysin and 4 bi-component leukocidins of Staphylococcus aureus with a single human monoclonal antibody.一石五鸟:一种人源单克隆抗体中和金黄色葡萄球菌的α-溶血素和4种双组分杀白细胞素
MAbs. 2015;7(1):243-54. doi: 10.4161/19420862.2014.985132.
8
α-Hemolysin activity of methicillin-susceptible Staphylococcus aureus predicts ventilator-associated pneumonia.耐甲氧西林金黄色葡萄球菌的α-溶血素活性可预测呼吸机相关性肺炎。
Am J Respir Crit Care Med. 2014 Nov 15;190(10):1139-48. doi: 10.1164/rccm.201406-1012OC.
9
Cytotoxic Virulence Predicts Mortality in Nosocomial Pneumonia Due to Methicillin-Resistant Staphylococcus aureus.细胞毒性毒力可预测耐甲氧西林金黄色葡萄球菌所致医院获得性肺炎的死亡率。
J Infect Dis. 2015 Jun 15;211(12):1862-74. doi: 10.1093/infdis/jiu554. Epub 2014 Oct 7.
10
Genomic responses in mouse models greatly mimic human inflammatory diseases.小鼠模型中的基因组反应极大地模拟了人类炎症性疾病。
Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):1167-72. doi: 10.1073/pnas.1401965111. Epub 2014 Aug 4.

靶向α毒素以减轻其在金黄色葡萄球菌坏死性肺炎雪貂和兔模型中的致死毒性。

Targeting Alpha Toxin To Mitigate Its Lethal Toxicity in Ferret and Rabbit Models of Staphylococcus aureus Necrotizing Pneumonia.

作者信息

Diep Binh An, Hilliard Jamese J, Le Vien T M, Tkaczyk Christine, Le Hoan N, Tran Vuvi G, Rao Renee L, Dip Etyene Castro, Pereira-Franchi Eliane P, Cha Paulyn, Jacobson Scott, Broome Rosemary, Cheng Lily I, Weiss William, Prokai Laszlo, Nguyen Vien, Stover C Ken, Sellman Bret R

机构信息

Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California, San Francisco, California, USA

Department of Infectious Diseases, MedImmune, LLC, Gaithersburg, Maryland, USA.

出版信息

Antimicrob Agents Chemother. 2017 Mar 24;61(4). doi: 10.1128/AAC.02456-16. Print 2017 Apr.

DOI:10.1128/AAC.02456-16
PMID:28115346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5365647/
Abstract

The role broad-spectrum antibiotics play in the spread of antimicrobial resistance, coupled with their effect on the healthy microbiome, has led to advances in pathogen-specific approaches for the prevention or treatment of serious bacterial infections. One approach in clinical testing is passive immunization with a monoclonal antibody (MAb) targeting alpha toxin for the prevention or treatment of pneumonia. Passive immunization with the human anti-alpha toxin MAb, MEDI4893*, has been shown to improve disease outcome in murine pneumonia models. The species specificity of some toxins necessitates testing anti- therapeutics in alternate species. We developed a necrotizing pneumonia model in ferrets and utilized an existing rabbit pneumonia model to characterize MEDI4893* protective activity in species other than mice. MEDI4893* prophylaxis reduced disease severity in ferret and rabbit pneumonia models against both community-associated methicillin-resistant (MRSA) and hospital-associated MRSA strains. In addition, adjunctive treatment of MEDI4893* with either vancomycin or linezolid provided enhanced protection in rabbits relative to the antibiotics alone. These results confirm that MEDI4893 is a promising candidate for immunotherapy against pneumonia.

摘要

广谱抗生素在抗菌药物耐药性传播中所起的作用,以及它们对健康微生物群的影响,促使针对严重细菌感染的预防或治疗的病原体特异性方法取得了进展。临床测试中的一种方法是使用靶向α毒素的单克隆抗体(MAb)进行被动免疫,以预防或治疗肺炎。已证明用人类抗α毒素单克隆抗体MEDI4893进行被动免疫可改善小鼠肺炎模型中的疾病结局。某些毒素的物种特异性使得有必要在其他物种中测试抗治疗药物。我们在雪貂中建立了坏死性肺炎模型,并利用现有的兔肺炎模型来表征MEDI4893在小鼠以外物种中的保护活性。MEDI4893预防可降低雪貂和兔肺炎模型中针对社区获得性耐甲氧西林(MRSA)和医院获得性MRSA菌株的疾病严重程度。此外,相对于单独使用抗生素,MEDI4893与万古霉素或利奈唑胺的辅助治疗在兔中提供了增强的保护作用。这些结果证实MEDI4893是肺炎免疫治疗的一个有前景的候选药物。