Berry Neil, Mee Edward T, Almond Neil, Rose Nicola J
Research & Development-Science, Research and Innovation, Medicines and Healthcare products Regulatory Agency, South Mimms, Hertfordshire EN6 3QG, UK.
Microorganisms. 2024 Jan 12;12(1):155. doi: 10.3390/microorganisms12010155.
Understanding infectious disease pathogenesis and evaluating novel candidate treatment interventions for human use frequently requires prior or parallel analysis in animal model systems. While rodent species are frequently applied in such studies, there are situations where non-human primate (NHP) species are advantageous or required. These include studies of animals that are anatomically more akin to humans, where there is a need to interrogate the complexity of more advanced biological systems or simply reflect susceptibility to a specific infectious agent. The contribution of different arms of the immune response may be addressed in a variety of NHP species or subspecies in specific physiological compartments. Such studies provide insights into immune repertoires not always possible from human studies. However, genetic variation in outbred NHP models may confound, or significantly impact the outcome of a particular study. Thus, host factors need to be considered when undertaking such studies. Considerable knowledge of the impact of host immunogenetics on infection dynamics was elucidated from HIV/SIV research. NHP models are now important for studies of emerging infections. They have contributed to delineating the pathogenesis of SARS-CoV-2/COVID-19, which identified differences in outcomes attributable to the selected NHP host. Moreover, their use was crucial in evaluating the immunogenicity and efficacy of vaccines against COVID-19 and establishing putative correlates of vaccine protection. More broadly, neglected or highly pathogenic emerging or re-emergent viruses may be studied in selected NHPs. These studies characterise protective immune responses following infection or the administration of candidate immunogens which may be central to the accelerated licensing of new vaccines. Here, we review selected aspects of host immunogenetics, specifically MHC background and TRIM5 polymorphism as exemplars of adaptive and innate immunity, in commonly used Old and New World host species. Understanding this variation within and between NHP species will ensure that this valuable laboratory source is used most effectively to combat established and emerging virus infections and improve human health worldwide.
了解传染病发病机制并评估用于人类的新型候选治疗干预措施通常需要在动物模型系统中进行预先或并行分析。虽然啮齿类动物经常用于此类研究,但在某些情况下,非人类灵长类动物(NHP)更具优势或必不可少。这些情况包括对解剖结构更类似于人类的动物进行研究,需要探究更先进生物系统的复杂性,或者仅仅是反映对特定传染原的易感性。免疫反应不同分支的作用可以在特定生理隔室中的多种NHP物种或亚种中进行研究。此类研究能够深入了解人类研究中不一定能获得的免疫库。然而,远交NHP模型中的基因变异可能会混淆或显著影响特定研究的结果。因此,在进行此类研究时需要考虑宿主因素。从HIV/SIV研究中阐明了宿主免疫遗传学对感染动态影响的大量知识。NHP模型现在对于新兴感染的研究很重要。它们有助于阐明SARS-CoV-2/COVID-19的发病机制,该研究确定了所选NHP宿主在结果上的差异。此外,它们的使用对于评估针对COVID-19疫苗的免疫原性和效力以及确定疫苗保护的假定相关因素至关重要。更广泛地说,可以在选定的NHP中研究被忽视的或高致病性的新兴或再发病毒。这些研究表征了感染或施用候选免疫原后产生的保护性免疫反应,这可能是新疫苗加速获批的关键。在这里,我们回顾了常用的旧世界和新世界宿主物种中宿主免疫遗传学的选定方面,特别是作为适应性和先天性免疫范例的MHC背景和TRIM5多态性。了解NHP物种内部和之间的这种变异将确保最有效地利用这一宝贵的实验室资源来对抗已有的和新兴的病毒感染,并改善全球人类健康。