Han Jiahe, Poma Alessandro
UCL Institute of Cardiovascular Science, The Rayne Building, 5 University Street, London WC1E 6JF, UK.
Division of Biomaterials and Tissue Engineering, UCL Eastman Dental Institute, Royal Free Hospital, UCL Medical School, Rowland Hill Street, London NW3 2PF, UK.
Polymers (Basel). 2022 Aug 5;14(15):3198. doi: 10.3390/polym14153198.
Infective endocarditis (IE) is a heart disease caused by the infection of heart valves, majorly caused by . IE is initiated by bacteria entering the blood circulation in favouring conditions (e.g., during invasive procedures). So far, the conventional antimicrobial strategies based on the usage of antibiotics remain the major intervention for treating IE. Nevertheless, the therapeutic efficacy of antibiotics in IE is limited not only by the bacterial drug resistance, but also by the formation of biofilms, which resist the penetration of antibiotics into bacterial cells. To overcome these drawbacks, the development of anti-biofilm treatments that can expose bacteria and make them more susceptible to the action of antibiotics, therefore resulting in reduced antimicrobial resistance, is urgently required. A series of anti-biofilm strategies have been developed, and this review will focus in particular on the development of anti-biofilm antibodies. Based on the results previously reported in the literature, several potential anti-biofilm targets are discussed, such as bacterial adhesins, biofilm matrix and bacterial toxins, covering their antigenic properties (with the identification of potential promising epitopes), functional mechanisms, as well as the antibodies already developed against these targets and, where feasible, their clinical translation.
感染性心内膜炎(IE)是一种由心脏瓣膜感染引起的心脏病,主要由……引起。IE是在有利条件下(如侵入性操作期间)细菌进入血液循环引发的。到目前为止,基于使用抗生素的传统抗菌策略仍然是治疗IE的主要干预措施。然而,抗生素在IE中的治疗效果不仅受到细菌耐药性的限制,还受到生物膜形成的限制,生物膜会阻碍抗生素渗透到细菌细胞中。为了克服这些缺点,迫切需要开发能够暴露细菌并使其对抗生素作用更敏感从而降低抗菌耐药性的抗生物膜治疗方法。已经开发了一系列抗生物膜策略,本综述将特别关注抗生物膜抗体的开发。基于先前文献报道的结果,讨论了几个潜在的抗生物膜靶点,如细菌黏附素、生物膜基质和细菌毒素,涵盖它们的抗原特性(确定潜在的有前景的表位)、功能机制,以及已经针对这些靶点开发的抗体,在可行的情况下还包括它们的临床转化。