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