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Advax佐剂重组保护性抗原可提供针对吸入性炭疽的保护作用,添加murabutide佐剂可进一步增强这种保护作用。

Advax-adjuvanted recombinant protective antigen provides protection against inhalational anthrax that is further enhanced by addition of murabutide adjuvant.

作者信息

Feinen Brandon, Petrovsky Nikolai, Verma Anita, Merkel Tod J

机构信息

Division of Bacterial, Parasitic and Allergenic Products, Center for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.

出版信息

Clin Vaccine Immunol. 2014 Apr;21(4):580-6. doi: 10.1128/CVI.00019-14. Epub 2014 Feb 19.

Abstract

Subunit vaccines against anthrax based on recombinant protective antigen (PA) potentially offer more consistent and less reactogenic anthrax vaccines but require adjuvants to achieve optimal immunogenicity. This study sought to determine in a murine model of pulmonary anthrax infection whether the polysaccharide adjuvant Advax or the innate immune adjuvant murabutide alone or together could enhance PA immunogenicity by comparison to an alum adjuvant. A single immunization with PA plus Advax adjuvant afforded significantly greater protection against aerosolized Bacillus anthracis Sterne strain 7702 than three immunizations with PA alone. Murabutide had a weaker adjuvant effect than Advax when used alone, but when murabutide was formulated together with Advax, an additive effect on immunogenicity and protection was observed, with complete protection after just two doses. The combined adjuvant formulation stimulated a robust, long-lasting B-cell memory response that protected mice against an aerosol challenge 18 months postimmunization with acceleration of the kinetics of the anamnestic IgG response to B. anthracis as reflected by ∼4-fold-higher anti-PA IgG titers by day 2 postchallenge versus mice that received PA with Alhydrogel. In addition, the combination of Advax plus murabutide induced approximately 3-fold-less inflammation than Alhydrogel as measured by in vivo imaging of cathepsin cleavage resulting from injection of ProSense 750. Thus, the combination of Advax and murabutide provided enhanced protection against inhalational anthrax with reduced localized inflammation, making this a promising next-generation anthrax vaccine adjuvanting strategy.

摘要

基于重组保护性抗原(PA)的炭疽亚单位疫苗可能提供更稳定且反应原性更低的炭疽疫苗,但需要佐剂来实现最佳免疫原性。本研究旨在通过与明矾佐剂比较,在肺部炭疽感染的小鼠模型中确定多糖佐剂Advax或先天免疫佐剂murabutide单独或联合使用是否能增强PA的免疫原性。与单独三次接种PA相比,单次接种PA加Advax佐剂对雾化的炭疽芽孢杆菌Sterne菌株7702提供了显著更强的保护。单独使用时,murabutide的佐剂效果比Advax弱,但当murabutide与Advax联合配制时,观察到对免疫原性和保护的相加作用,仅两剂后即可提供完全保护。联合佐剂配方刺激了强大、持久的B细胞记忆反应,可保护小鼠在免疫后18个月免受气溶胶攻击,加速了对炭疽芽孢杆菌的回忆性IgG反应动力学,如在攻击后第2天,与接受PA加氢氧化铝凝胶的小鼠相比,抗PA IgG滴度高约4倍。此外,通过对注射ProSense 750后组织蛋白酶裂解的体内成像测量,Advax加murabutide的组合诱导的炎症比氢氧化铝凝胶少约3倍。因此,Advax和murabutide的组合提供了针对吸入性炭疽的增强保护,同时减少了局部炎症,使其成为一种有前景的下一代炭疽疫苗佐剂策略。

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