Department of Animal, Dairy and Veterinary Sciences, Center for Integrated BioSystems, College of Veterinary Medicine, Utah State University, Logan, UT, United States.
Utah Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Utah State University, Logan, UT, United States.
Front Endocrinol (Lausanne). 2023 Jan 23;14:1066356. doi: 10.3389/fendo.2023.1066356. eCollection 2023.
Aging leads to a general decline in protective immunity. The most common age-associated effects are in seen T-cell mediated immune function. Adult mice whose immune systems show only moderate changes in T-cell subsets tend to live longer than age-matched siblings that display extensive T-cell subset aging. Importantly, at the time of reproductive decline, the increase in disease risks in women significantly outpace those of men. In female mice, there is a significant decline in central and peripheral naïve T-cell subsets at the time of reproductive failure. Available evidence indicates that this naïve T-cell decline is sensitive to ovarian function and can be reversed in post-reproductive females by transplantation of young ovaries. The restoration of naïve T-cell subsets due to ovarian transplantation was impressive compared with post-reproductive control mice, but represented only a partial recovery of what was lost from 6 months of age. Apparently, the influence of ovarian function on immune function may be an indirect effect, likely moderated by other physiological functions. Estradiol is significantly reduced in post-reproductive females, but was not increased in post-reproductive females that received new ovaries, suggesting an estradiol-independent, but ovarian-dependent influence on immune function. Further evidence for an estradiol-independent influence includes the restoration of immune function through the transplantation of young ovaries depleted of follicles and through the injection of isolated ovarian somatic cells into the senescent ovaries of old mice. While the restoration of naïve T-cell populations represents only a small part of the immune system, the ability to reverse this important functional parameter independent of estradiol may hold promise for the improvement of post-reproductive female immune health. Further studies of the non-reproductive influence of the ovary will be needed to elucidate the mechanisms of the relationship between the ovary and health.
衰老是导致保护性免疫普遍下降的原因。最常见的与年龄相关的影响见于 T 细胞介导的免疫功能。免疫系统中 T 细胞亚群只有适度变化的成年小鼠往往比显示广泛 T 细胞亚群衰老的同龄兄弟姐妹寿命更长。重要的是,在生殖衰退时,女性疾病风险的增加明显超过男性。在雌性小鼠中,在生殖衰竭时,中枢和外周幼稚 T 细胞亚群明显减少。现有证据表明,这种幼稚 T 细胞的减少对卵巢功能敏感,可以通过移植年轻的卵巢来逆转生殖后雌性小鼠的这种减少。与生殖后对照小鼠相比,由于卵巢移植而恢复幼稚 T 细胞亚群的效果令人印象深刻,但仅代表了从 6 个月龄开始失去的部分恢复。显然,卵巢功能对免疫功能的影响可能是一种间接影响,可能由其他生理功能调节。生殖后雌性小鼠的雌二醇明显减少,但接受新卵巢的生殖后雌性小鼠的雌二醇没有增加,这表明雌二醇独立但卵巢依赖对免疫功能的影响。雌二醇独立影响的进一步证据包括通过移植缺乏卵泡的年轻卵巢和通过将分离的卵巢体细胞注射到老年小鼠衰老的卵巢中恢复免疫功能。虽然幼稚 T 细胞群体的恢复仅代表免疫系统的一小部分,但能够独立于雌二醇恢复这一重要功能参数可能为改善生殖后女性免疫健康带来希望。需要进一步研究卵巢的非生殖影响,以阐明卵巢与健康之间关系的机制。