Measuring thymic output across the human lifespan: a critical challenge in laboratory medicine

IF 5.4 2区 医学 Q1 GERIATRICS & GERONTOLOGY GeroScience Pub Date : 2025-02-13 DOI:10.1007/s11357-025-01555-3
Vera Middelkamp, Eliisa Kekäläinen
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Abstract

Age-associated thymic involution leads to a significant decline in thymic T cell output, a major contributor to immunosenescence in the elderly. Accurately measuring thymic output is therefore critical for understanding the mechanisms behind immune aging. Furthermore, robust quantification of thymic output is essential in various other clinical and research settings, including the diagnosis of immunodeficiencies and the monitoring of T cell reconstitution following therapeutic interventions like hematopoietic stem cell transplantation. Current methodologies for measuring thymic output include T cell receptor excision circle (TREC) quantification via quantitative polymerase chain reaction and the enumeration of recent thymic emigrants (RTEs) using flow cytometry. However, TREC-based assays are inherently insensitive to subtle changes in thymic output, limiting their applicability beyond neonatal immunodeficiency screening. Similarly, RTE enumeration presents challenges; while surface markers exist for CD4⁺ RTEs, validated markers for CD8⁺ cytotoxic T lymphocytes are lacking. This represents a significant knowledge gap, particularly as aging has been shown to disproportionally affect the CD8 T cell pool. Moreover, while flow cytometry effectively measures mature naïve T cells, these cells do not accurately represent real-time thymic output, as they can persist in peripheral circulation for extended periods. These limitations highlight the pressing need for more accurate and sensitive methods to assess thymic output. Improved measurement techniques would not only enhance our understanding of thymic involution in the context of aging but also enable large-scale investigations into thymic function and the mechanisms driving its decline in both health and disease. In this review, we examine current methodologies for measuring thymic output in humans, critically evaluate their limitations, and discuss emerging approaches to address these gaps in the field.

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测量人类一生的胸腺输出:实验室医学的一个关键挑战
年龄相关的胸腺退化导致胸腺T细胞输出显著下降,这是老年人免疫衰老的主要原因。因此,准确测量胸腺输出对于理解免疫衰老背后的机制至关重要。此外,胸腺输出量的强大量化在各种其他临床和研究环境中是必不可少的,包括免疫缺陷的诊断和治疗干预(如造血干细胞移植)后T细胞重建的监测。目前测量胸腺输出量的方法包括通过定量聚合酶链反应定量T细胞受体切除环(TREC)和使用流式细胞术计数最近胸腺迁移(rte)。然而,基于trec的检测天生对胸腺输出的细微变化不敏感,限制了其在新生儿免疫缺陷筛查之外的适用性。同样,RTE枚举也带来了挑战;虽然存在CD4 + rte的表面标记物,但缺乏CD8 +细胞毒性T淋巴细胞的有效标记物。这代表了一个重要的知识差距,特别是当衰老被证明不成比例地影响CD8 T细胞池时。此外,虽然流式细胞术有效地测量成熟naïve T细胞,但这些细胞不能准确地代表实时胸腺输出,因为它们可以在外周循环中持续很长时间。这些限制突出了迫切需要更准确和敏感的方法来评估胸腺输出。改进的测量技术不仅可以增强我们对衰老背景下胸腺退化的理解,还可以对胸腺功能及其在健康和疾病中导致其衰退的机制进行大规模研究。在这篇综述中,我们研究了目前测量人类胸腺输出的方法,批判性地评估了它们的局限性,并讨论了解决这些领域空白的新方法。
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来源期刊
GeroScience
GeroScience Medicine-Complementary and Alternative Medicine
CiteScore
10.50
自引率
5.40%
发文量
182
期刊介绍: GeroScience is a bi-monthly, international, peer-reviewed journal that publishes articles related to research in the biology of aging and research on biomedical applications that impact aging. The scope of articles to be considered include evolutionary biology, biophysics, genetics, genomics, proteomics, molecular biology, cell biology, biochemistry, endocrinology, immunology, physiology, pharmacology, neuroscience, and psychology.
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