Michigan State University, East Lansing, Michigan, USA.
Michigan State University, East Lansing, Michigan, USA
Infect Immun. 2020 Jun 22;88(7). doi: 10.1128/IAI.00916-19.
Chronic bacterial infections are caused by pathogens that persist within their hosts and avoid clearance by the immune system. Treatment and/or detection of such pathogens is difficult, and the resulting pathologies are often deleterious or fatal. There is an urgent need to develop protective vaccines and host-directed therapies that synergize with antibiotics to prevent pathogen persistence and infection-associated pathologies. However, many persistent pathogens, such as , actively target the very host pathways activated by vaccination. These immune evasion tactics blunt the effectiveness of immunization strategies and are impeding progress to control these infections throughout the world. Therefore, it is essential that immune evasion-related pathogen virulence strategies are considered to maximize the effectiveness of potential new treatments. In this review, we focus on how infects antigen-presenting cells and evades effective immune clearance by the adaptive response through (i) manipulating antigen presentation, (ii) repressing T cell-activating costimulatory molecules, and (iii) inducing ligands that drive T cell exhaustion. In this context, we will examine the challenges that bacterial virulence strategies pose to developing new vaccines. We will then discuss new approaches that will help dissect immune evasion mechanisms and devise strategies to bypass them to promote long-term protection and prevent disease progression.
慢性细菌性感染是由病原体引起的,这些病原体在宿主体内持续存在,并逃避免疫系统的清除。治疗和/或检测这些病原体很困难,由此产生的病变通常是有害的或致命的。迫切需要开发保护性疫苗和宿主定向疗法,与抗生素协同作用,以防止病原体持续存在和感染相关的病变。然而,许多持续性病原体,如 ,积极针对疫苗接种激活的宿主途径。这些免疫逃避策略削弱了免疫接种策略的有效性,并阻碍了在全球范围内控制这些感染的进展。因此,必须考虑与免疫逃避相关的病原体毒力策略,以最大限度地提高潜在新疗法的有效性。在这篇综述中,我们重点关注 如何感染抗原呈递细胞,并通过(i)操纵抗原呈递、(ii)抑制 T 细胞激活共刺激分子和(iii)诱导驱动 T 细胞耗竭的配体,从而逃避适应性反应的有效免疫清除。在这种情况下,我们将研究细菌毒力策略对开发新疫苗带来的挑战。然后,我们将讨论有助于剖析 免疫逃避机制并设计绕过这些机制的策略的新方法,以促进长期保护和防止疾病进展。