Department of Pharmacology and Toxicology, Medical University of Sofia, 1431 Sofia, Bulgaria.
Division of Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Int J Mol Sci. 2021 May 27;22(11):5729. doi: 10.3390/ijms22115729.
The cutaneous immune response is important for the regulation of skin aging well as for the development of immune-mediated skin diseases. Aging of the human skin undergoes immunosenescence with immunological alterations and can be affected by environmental stressors and internal factors, thus leading to various epidermal barrier abnormalities. The dysfunctional epidermal barrier, immune dysregulation, and skin dysbiosis in the advanced age, together with the genetic factors, facilitate the late onset of atopic dermatitis (AD) in the elderly, whose cases have recently been on the rise. Controversial to the healthy aged skin, where overproduction of many cytokines is found, the levels of Th2/Th22 related cytokines inversely correlated with age in the skin of older AD patients. As opposed to an endogenously aged skin, the expression of the terminal differentiation markers significantly increases with age in AD. Despite the atenuated barrier disturbances in older AD patients, the aged skin carries an impairment associated with the aging process, which reflects the persistence of AD. The chronicity of AD in older patients might not directly affect skin aging but does not allow spontaneous remission. Thus, adult- and elderly subtypes of AD are considered as a lifelong disease.
皮肤的免疫反应对于调节皮肤衰老以及免疫介导性皮肤疾病的发展非常重要。人类皮肤的衰老经历免疫衰老,免疫改变,并可能受到环境应激源和内部因素的影响,从而导致各种表皮屏障异常。在高龄时,功能失调的表皮屏障、免疫失调和皮肤微生态失调,以及遗传因素,促使老年特应性皮炎(AD)的迟发性发作,老年 AD 的病例最近有所增加。与健康老年皮肤不同,健康老年皮肤中发现许多细胞因子过度产生,而在老年 AD 患者的皮肤中,Th2/Th22 相关细胞因子的水平与年龄呈反比。与内源性衰老皮肤相反,AD 患者的终末分化标志物的表达随年龄显著增加。尽管老年 AD 患者的屏障障碍减弱,但衰老皮肤与衰老过程相关的损伤仍然存在,这反映了 AD 的持续性。老年患者 AD 的慢性病程可能不会直接影响皮肤衰老,但不允许自发缓解。因此,成人和老年 AD 亚型被认为是一种终身疾病。