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用包含 O 特异性多糖和破伤风毒素重链重组片段的霍乱结合疫苗给兔子接种可诱导针对霍乱弧菌 O1 的保护性免疫应答。

Vaccination of Rabbits with a Cholera Conjugate Vaccine Comprising O-Specific Polysaccharide and a Recombinant Fragment of Tetanus Toxin Heavy Chain Induces Protective Immune Responses against Vibrio cholerae O1.

机构信息

Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts.

Eubiologics Ltd, Gangnam-gu, Seoul, South Korea.

出版信息

Am J Trop Med Hyg. 2023 Oct 2;109(5):1122-1128. doi: 10.4269/ajtmh.23-0259. Print 2023 Nov 1.

Abstract

There is a need for next-generation cholera vaccines that provide high-level and durable protection in young children in cholera-endemic areas. A cholera conjugate vaccine (CCV) is in development to address this need. This vaccine contains the O-specific polysaccharide (OSP) of Vibrio cholerae O1 conjugated via squaric acid chemistry to a recombinant fragment of the tetanus toxin heavy chain (OSP:rTTHc). This vaccine has been shown previously to be immunogenic and protective in mice and found to be safe in a recent preclinical toxicological analysis in rabbits. We took advantage of excess serum samples collected as part of the toxicological study and assessed the immunogenicity of CCV OSP:rTTHc in rabbits. We found that vaccination with CCV induced OSP-, lipopolysaccharide (LPS)-, and rTTHc-specific immune responses in rabbits, that immune responses were functional as assessed by vibriocidal activity, and that immune responses were protective against death in an established virulent challenge assay. CCV OSP:rTTHc immunogenicity in two animal model systems (mice and rabbits) is encouraging and supports further development of this vaccine for evaluation in humans.

摘要

需要开发下一代霍乱疫苗,为霍乱流行地区的幼儿提供高水平和持久的保护。目前正在开发一种霍乱结合疫苗(CCV)来满足这一需求。该疫苗包含霍乱弧菌 O1 的 O 特异性多糖(OSP),通过丁烯二酸化学与破伤风毒素重链的重组片段(OSP:rTTHc)连接。该疫苗先前已在小鼠中显示出免疫原性和保护作用,并在最近的兔临床前毒理学分析中发现安全。我们利用作为毒理学研究一部分收集的多余血清样本,评估了 CCV OSP:rTTHc 在兔中的免疫原性。我们发现,CCV 疫苗接种可诱导兔的 OSP、脂多糖(LPS)和 rTTHc 特异性免疫应答,免疫应答是功能性的,可通过杀菌活性评估,并且可预防在既定的强毒力挑战试验中死亡。CCV OSP:rTTHc 在两种动物模型系统(小鼠和兔)中的免疫原性令人鼓舞,支持进一步开发该疫苗进行人体评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abfb/10622467/25f94accc8e7/ajtmh.23-0259f1.jpg

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