Franceschi Claudio, Capri Miriam, Monti Daniela, Giunta Sergio, Olivieri Fabiola, Sevini Federica, Panourgia Maria Panagiota, Invidia Laura, Celani Laura, Scurti Maria, Cevenini Elisa, Castellani Gastone C, Salvioli Stefano
Department of Experimental Pathology, University of Bologna, via S. Giacomo 12, 40126 Bologna, Italy.
Mech Ageing Dev. 2007 Jan;128(1):92-105. doi: 10.1016/j.mad.2006.11.016. Epub 2006 Nov 20.
A large part of the aging phenotype, including immunosenescence, is explained by an imbalance between inflammatory and anti-inflammatory networks, which results in the low grade chronic pro-inflammatory status we proposed to call inflammaging. Within this perspective, healthy aging and longevity are likely the result not only of a lower propensity to mount inflammatory responses but also of efficient anti-inflammatory networks, which in normal aging fail to fully neutralize the inflammatory processes consequent to the lifelong antigenic burden and exposure to damaging agents. Such a global imbalance can be a major driving force for frailty and common age-related pathologies, and should be addressed and studied within an evolutionary-based systems biology perspective. Evidence in favor of this conceptualization largely derives from studies in humans. We thus propose that inflammaging can be flanked by anti-inflammaging as major determinants not only of immunosenescence but eventually of global aging and longevity.
衰老表型的很大一部分,包括免疫衰老,是由炎症和抗炎网络之间的失衡所解释的,这种失衡导致了我们提出称之为炎症衰老的低度慢性促炎状态。从这个角度来看,健康衰老和长寿可能不仅是炎症反应倾向较低的结果,也是高效抗炎网络的结果,在正常衰老过程中,这些抗炎网络无法完全中和由于终身抗原负担和接触损伤因子而产生的炎症过程。这种全局失衡可能是虚弱和常见年龄相关疾病的主要驱动力,应该在基于进化的系统生物学视角下进行研究和探讨。支持这一概念的证据很大程度上来自对人类的研究。因此,我们提出,炎症衰老可以与抗炎症衰老一起,作为不仅是免疫衰老而且最终是全局衰老和长寿的主要决定因素。