Center for Vaccine Development; University of Maryland School of Medicine; Baltimore, MD USA.
Virulence. 2014 Jan 1;5(1):219-25. doi: 10.4161/viru.25965. Epub 2013 Aug 13.
Gram-negative bacterial (GNB) infections are a leading cause of serious infections both in hospitals and the community. The mortality remains high despite potent antimicrobials and modern supportive care. In the last decade invasive GNB have become increasingly resistant to commonly used antibiotics, and attempts to intervene with novel biological therapies have been unsuccessful. Earlier studies with antibodies directed against a highly conserved core region in the GNB lipopolysaccharide (LPS, or endotoxin) suggested that this approach may have therapeutic benefit, and led to the development of a subunit vaccine that has progressed to phase 1 clinical testing. Since only a few serogroups of GNB cause bacteremia, O-specific vaccines had been developed, but these were not deployed because of the availability of other therapeutic options at the time. Given the likelihood that new antibiotics will not be soon available, the development of vaccines and antibodies directed against endotoxin, both O and core antigens, deserves a "second look".
革兰氏阴性菌(GNB)感染是医院和社区严重感染的主要原因。尽管有强效的抗生素和现代支持性治疗,但死亡率仍然很高。在过去的十年中,侵袭性 GNB 对常用抗生素的耐药性日益增强,而尝试使用新型生物疗法干预的尝试也没有成功。早期的研究表明,针对 GNB 脂多糖(LPS,或内毒素)中高度保守核心区域的抗体可能具有治疗益处,并导致开发出一种已进入 1 期临床测试的亚单位疫苗。由于只有少数 GNB 血清群引起菌血症,因此已经开发了 O 特异性疫苗,但由于当时有其他治疗选择,因此并未使用这些疫苗。鉴于新抗生素不太可能很快问世,针对内毒素(包括 O 抗原和核心抗原)的疫苗和抗体的开发值得“重新审视”。