Laboratory of Immunology, National Institute on Aging, NIH, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.
Curr Opin Pharmacol. 2010 Aug;10(4):408-24. doi: 10.1016/j.coph.2010.04.015. Epub 2010 Jun 4.
One of the major fundamental causes for the aging of the immune system is the structural and functional involution of the thymus, and the associated decline in de novo naïve T-lymphocyte output. This loss of naïve T-cell production weakens the ability of the adaptive immune system to respond to new antigenic stimuli and eventually leads to a peripheral T-cell bias to the memory phenotype. While the precise mechanisms responsible for age-associated thymic involution remain unknown, a variety of theories have been forwarded including the loss of expression of various growth factors and hormones that influence the lymphoid compartment and promote thymic function. Extensive studies examining two hormones, namely growth hormone (GH) and ghrelin (GRL), have demonstrated their contributions to thymus biology. In the current review, we discuss the literature supporting a role for these hormones in thymic physiology and age-associated thymic involution and their potential use in the restoration of thymic function in aged and immunocompromised individuals.
免疫系统衰老的一个主要根本原因是胸腺的结构和功能退化,以及新的幼稚 T 淋巴细胞生成能力的相关下降。这种幼稚 T 细胞生成的丧失削弱了适应性免疫系统对新抗原刺激的反应能力,最终导致外周 T 细胞偏向于记忆表型。尽管导致与年龄相关的胸腺退化的确切机制尚不清楚,但已经提出了多种理论,包括各种影响淋巴组织并促进胸腺功能的生长因子和激素表达的丧失。大量研究检查了两种激素,即生长激素 (GH) 和胃饥饿素 (GRL),证明了它们对胸腺生物学的贡献。在本综述中,我们讨论了支持这些激素在胸腺生理学和与年龄相关的胸腺退化中的作用的文献,以及它们在恢复老年和免疫功能低下个体的胸腺功能方面的潜在用途。