Garcia Amanda K, Almodovar Sharilyn
Department of Immunology & Molecular Microbiology, Texas Tech University Health Sciences Center, School of Medicine, Lubbock, TX 79430, USA.
Center for Tropical Medicine & Infectious Diseases, Texas Tech University Health Sciences Center, School of Medicine, Lubbock, TX 79430, USA.
J Vasc Dis. 2024 Jun;3(2):174-200. doi: 10.3390/jvd3020015. Epub 2024 May 6.
People living with HIV (PLWH) face a growing burden of chronic diseases, owing to the combinations of aging, environmental triggers, lifestyle choices, and virus-induced chronic inflammation. The rising incidence of pulmonary vascular diseases represents a major concern for PLWH. The study of HIV-associated pulmonary vascular complications ideally requires a strong understanding of pulmonary vascular cell biology and HIV pathogenesis at the molecular level for effective applications in infectious diseases and vascular medicine. Active HIV infection and/or HIV proteins disturb the delicate balance between vascular tone and constriction, which is pivotal for maintaining pulmonary vascular health. One of the defining features of HIV is its high genetic diversity owing to several factors including its high mutation rate, recombination between viral strains, immune selective pressures, or even geographical factors. The intrinsic HIV genetic diversity has several important implications for pathogenic outcomes of infection and the overall battle to combat HIV. Challenges in the field present themselves from two sides of the same coin: those imposed by the virus itself and those stemming from the host. The field may be advanced by further developing and in vitro models that are well described for both pulmonary vascular diseases and HIV for mechanistic studies. In essence, the study of HIV-associated pulmonary vascular complications requires a multidisciplinary approach, drawing upon insights from both infectious diseases and vascular medicine. In this review article, we discuss the fundamentals of HIV virology and their impact on pulmonary disease, aiming to enhance the understanding of either area or both simultaneously. Bridging the gap between preclinical research findings and clinical practice is essential for improving patient care. Addressing these knowledge gaps requires interdisciplinary collaborations, innovative research approaches, and dedicated efforts to prioritize HIV-related pulmonary complications on the global research agenda.
由于衰老、环境诱因、生活方式选择以及病毒诱导的慢性炎症等多种因素的综合作用,艾滋病毒感染者(PLWH)面临着日益加重的慢性病负担。肺血管疾病发病率的上升是PLWH面临的一个主要问题。理想情况下,对与艾滋病毒相关的肺血管并发症的研究需要在分子水平上深入了解肺血管细胞生物学和艾滋病毒发病机制,以便在传染病和血管医学中有效应用。活跃的艾滋病毒感染和/或艾滋病毒蛋白会破坏血管张力与收缩之间的微妙平衡,而这种平衡对于维持肺血管健康至关重要。艾滋病毒的一个显著特征是其高度的遗传多样性,这是由多种因素造成的,包括其高突变率、病毒株之间的重组、免疫选择压力,甚至地理因素。艾滋病毒固有的遗传多样性对感染的致病结果以及抗击艾滋病毒的总体斗争具有若干重要影响。该领域的挑战来自同一枚硬币的两面:病毒本身带来的挑战以及宿主引发的挑战。通过进一步开发和体外模型可以推动该领域的发展,这些模型在肺血管疾病和艾滋病毒方面都有很好的描述,可用于机制研究。从本质上讲,对与艾滋病毒相关的肺血管并发症的研究需要采用多学科方法,借鉴传染病和血管医学的见解。在这篇综述文章中,我们讨论了艾滋病毒病毒学的基本原理及其对肺部疾病的影响,旨在同时增进对这两个领域的理解。弥合临床前研究结果与临床实践之间的差距对于改善患者护理至关重要。解决这些知识差距需要跨学科合作、创新的研究方法以及在全球研究议程上优先考虑与艾滋病毒相关的肺部并发症的专门努力。