Shive Carey, Pandiyan Pushpa
Louis Stokes Cleveland VA Medical Center, United States Department of Veterans Affairs, Cleveland, OH, United States.
Case Western Reserve University, Cleveland, OH, United States.
Front Aging. 2022 Apr 27;3:840827. doi: 10.3389/fragi.2022.840827. eCollection 2022.
An optimal immune response requires the appropriate interaction between the innate and the adaptive arms of the immune system as well as a proper balance of activation and regulation. After decades of life, the aging immune system is continuously exposed to immune stressors and inflammatory assaults that lead to immune senescence. In this review, we will discuss inflammaging in the elderly, specifically concentrating on IL-6 and IL-1b in the context of T lymphocytes, and how inflammation is related to mortality and morbidities, specifically cardiovascular disease and cancer. Although a number of studies suggests that the anti-inflammatory cytokine TGF-b is elevated in the elderly, heightened inflammation persists. Thus, the regulation of the immune response and the ability to return the immune system to homeostasis is also important. Therefore, we will discuss cellular alterations in aging, concentrating on senescent T cells and CD4+ CD25+ FOXP3+ regulatory T cells (Tregs) in aging.
最佳免疫反应需要免疫系统的固有免疫和适应性免疫分支之间进行适当的相互作用,以及激活与调节之间的适当平衡。经过数十年的生命历程,衰老的免疫系统持续暴露于免疫应激源和炎症攻击之下,从而导致免疫衰老。在本综述中,我们将讨论老年人的炎症衰老,特别关注T淋巴细胞背景下的白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β),以及炎症与死亡率和发病率(特别是心血管疾病和癌症)之间的关系。尽管多项研究表明抗炎细胞因子转化生长因子-β(TGF-β)在老年人中升高,但炎症加剧的情况仍然存在。因此,免疫反应的调节以及使免疫系统恢复稳态的能力也很重要。所以,我们将讨论衰老过程中的细胞变化,重点关注衰老的T细胞和衰老过程中的CD4+ CD25+ FOXP3+调节性T细胞(Tregs)。