Institute of Public Health, Semmelweis University, Budapest, Hungary.
Immun Ageing. 2010 Jun 14;7:7. doi: 10.1186/1742-4933-7-7.
The increasing ratio of ageing population poses new challenges to healthcare systems. The elderly frequently suffer from severe infections. Vaccination could protect them against several infectious diseases, but it can be effective only if cells that are capable of responding are still present in the repertoire. Recent vaccination strategies in the elderly might achieve low effectiveness due to age-related immune impairment. Immunosenescence affects both the innate and adaptive immunity.Beside individual variations of genetic predisposition, epigenetic changes over the full course of human life exert immunomodulating effects. Disturbances in macrophage-derived cytokine release and reduction of the natural killer cell mediated cytotoxicity lead to increased frequency of infections. Ageing dampens the ability of B cells to produce antibodies against novel antigens. Exhausted memory B lymphocyte subsets replace naïve cells. Decline of cell-mediated immunity is the consequence of multiple changes, including thymic atrophy, reduced output of new T lymphocytes, accumulation of anergic memory cells, and deficiencies in cytokines production. Persistent viral and parasitic infections contribute to the loss of immunosurveillance and premature exhaustion of T cells. Reduced telomerase activity and Toll-like receptor expression can be improved by chemotherapy. Reversion of thymic atrophy could be achieved by thymus transplantation, depletion of accumulated dysfunctional naive T cells and herpesvirus-specific exhausted memory cells. Administration of interleukin (IL)-2, IL-7, IL-10, keratinocyte growth factor, thymic stromal lymphopoietin, as well as leptin and growth hormone boost thymopoiesis. In animals, several strategies have been explored to produce superior vaccines. Among them, virosomal vaccines containing polypeptide antigens or DNA plasmids as well as new adjuvanted vaccine formulations elicit higher dendritic cell activity and more effective serologic than conventional vaccines responses in the elderly. Hopefully, at least some of these approaches can be translated to human medicine in a not too far future.
人口老龄化比例的增加给医疗保健系统带来了新的挑战。老年人经常患有严重的感染。疫苗接种可以保护他们免受几种传染病的侵害,但只有在反应细胞仍然存在的情况下,疫苗才会有效。由于与年龄相关的免疫功能受损,老年人最近的疫苗接种策略可能效果不佳。免疫衰老影响固有免疫和适应性免疫。除了个体遗传易感性的个体差异外,人类生命全过程中的表观遗传变化也会产生免疫调节作用。巨噬细胞衍生细胞因子释放的紊乱和自然杀伤细胞介导的细胞毒性的减少导致感染频率增加。衰老削弱了 B 细胞产生针对新抗原的抗体的能力。耗尽的记忆 B 淋巴细胞亚群取代了幼稚细胞。细胞介导的免疫能力下降是多种变化的结果,包括胸腺萎缩、新 T 淋巴细胞产生减少、无反应性记忆细胞积累以及细胞因子产生缺陷。持续性病毒和寄生虫感染导致免疫监视丧失和 T 细胞过早衰竭。端粒酶活性和 Toll 样受体表达的降低可以通过化疗得到改善。通过胸腺移植、耗尽积累的功能失调的幼稚 T 细胞和疱疹病毒特异性耗尽的记忆细胞,可以实现胸腺萎缩的逆转。白细胞介素 (IL)-2、IL-7、IL-10、角质形成细胞生长因子、胸腺基质淋巴生成素以及瘦素和生长激素可促进胸腺生成。在动物中,已经探索了几种策略来生产更好的疫苗。其中,含有多肽抗原或 DNA 质粒的类病毒疫苗以及新的佐剂疫苗配方在老年人中引起更高的树突状细胞活性和更有效的血清学反应,优于传统疫苗。希望在不久的将来,至少其中一些方法可以转化为人类医学。