以哥伦比亚酸和唾液酸为原型制备抗无乳链球菌和鲍曼不动杆菌二价疫苗的初步研究

Marcelio Oliveira, M. B. Corrêa, M. Leal, B. Silva, E. Jessouroun
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引用次数: 0

摘要

简介:生物偶联反应在一些不同化学物质在新的组装结构中的分子排列中起着重要的作用。这种结构在疫苗学领域对重要病原体具有重要意义。病原体无乳链球菌似乎是新生儿侵袭性感染的威胁,是几个国家的共同问题。同样,鲍曼不动杆菌一直是巴西医院的一个问题,主要原因是对不同抗菌素药物的耐药性日益增强。因此,使用结合二价疫苗作为预防这类病原体引起的医院感染的一种解决方案。因此,开发合成二价疫苗的新化学方法势在必行。实现了利用模拟无乳链球菌基质中官能团的原型来开发新的氧化方法的第一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preliminary studies of reactions using colominic and sialic acids as prototypes to bivalent vaccine against S. agalactiae and A. baumannii
Introduction: Bioconjugation reactions play an important role in developing molecular arrangement of some different chemical species in new assembled structures. Such structures are of great importance in the vaccinology field against important pathogens. The pathogen S. agalactiae appears as a threat of invasive infection in neonates, characterizing a common problem to several countries. Similarly, the bacterium A. baumannii has been a problem in Brazilian hospitals, mainly due to the increasing development of resistance to different antimicrobial drugs. Therefore, a use of conjugate bivalent vaccines rises as an answer to prevention of nosocomial infections caused by this kind of pathogens. Hence, the development of new chemical approaches for synthesis of bivalent vaccines is imperative. A primary step for development of new methodologies about oxidation using prototypes that mimic functional groups present in S. agalactiae matrix was realized.
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