Murray Michelle A, Chotirmall Sanjay H
Department of Respiratory Medicine, Mater Misericordiae Hospital, Eccles Street, Dublin 7, Ireland.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 308232.
Mediators Inflamm. 2015;2015:692546. doi: 10.1155/2015/692546. Epub 2015 Jun 23.
The global population is aging with significant gains in life expectancy particularly in the developed world. Consequently, greater focus on understanding the processes that underlie physiological aging has occurred. Key facets of advancing age include genomic instability, telomere shortening, epigenetic changes, and declines in immune function termed immunosenescence. Immunosenescence and its associated chronic low grade systemic "inflamm-aging" contribute to the development and progression of pulmonary disease in older individuals. These physiological processes predispose to pulmonary infection and confer specific and unique clinical phenotypes observed in chronic respiratory disease including late-onset asthma, chronic obstructive pulmonary disease, and pulmonary fibrosis. Emerging concepts of the gut and airway microbiome further complicate the interrelationship between host and microorganism particularly from an immunological perspective and especially so in the setting of immunosenescence. This review focuses on our current understanding of the aging process, immunosenescence, and how it can potentially impact on various pulmonary diseases and the human microbiome.
全球人口正在老龄化,预期寿命显著提高,尤其是在发达国家。因此,人们更加关注了解生理衰老背后的过程。衰老的关键方面包括基因组不稳定、端粒缩短、表观遗传变化以及免疫功能下降,即免疫衰老。免疫衰老及其相关的慢性低度全身性“炎症衰老”促进了老年人肺部疾病的发生和发展。这些生理过程易引发肺部感染,并导致在慢性呼吸道疾病中观察到的特定且独特的临床表型,包括迟发性哮喘、慢性阻塞性肺疾病和肺纤维化。肠道和气道微生物群的新观念进一步使宿主与微生物之间的相互关系复杂化,特别是从免疫学角度来看,在免疫衰老的情况下更是如此。本综述重点关注我们目前对衰老过程、免疫衰老及其如何可能影响各种肺部疾病和人类微生物群的理解。