Direct Evidence for Thymic Function in Adult Humans

• DOI: 10.1084/jem.190.4.479
• Publication Date: 2002-07-26T16:48:33Z
• Authors: Jean-François Poulin; Mohan N. Viswanathan; Jeffrey M. Harris; Krishna V. Komanduri; Eric Wieder; Nancy Ringuette; Morgan Jenkins; Joseph M. McCune; Rafick-Pierre Sékaly
• Keywords: Adult; Aging; Biomedical and clinical sciences; 1.1 Normal biological development and functioning; Receptors, Antigen, T-Cell, alpha-beta; Immunology; 610; Thymus Gland; Medical and Health Sciences; Mice; 03 medical and health sciences; Clinical Research; Underpinning research; thymus; T-Lymphocyte Subsets; 616; Receptors; T-Cell Receptor beta; 2.1 Biological and endogenous factors; Animals; Humans; deletion circles; Aetiology; L-Selectin; Aged; Sequence Deletion; alpha-beta; 0303 health sciences; Biomedical and Clinical Sciences; Health sciences; immune reconstitution; Middle Aged; T-Cell; Fetal Blood; Flow Cytometry; naive T cells; Phenotype; Genes; Antigen; CD4 Antigens; Genes, T-Cell Receptor beta; Leukocyte Common Antigens; T cell receptor

The understanding of human thymic function and evaluation of its contribution to T cell homeostasis are matters of great importance. Here we report the development of a novel assay to quantitate the frequency and diversity of recent thymic emigrants (RTEs) in the peripheral blood of humans. Such cells were defined by the presence of T cell receptor (TCR) rearrangement deletion circles (DCs), episomal byproducts of TCR-β V(D)J rearrangement. DCs were detected in T cells in the thymus, cord blood, and adult peripheral blood. In the peripheral blood of adults aged 22 to 76 years, their frequency was highest in the CD4+CD45RA+ CD62L+ subpopulation of naive T cells. TCR DCs were also observed in other subpopulations of peripheral blood T cells, including those with the CD4+CD45RO−CD62L+ and CD4+CD45RO+CD62L+ phenotypes. RTEs were observed to have more than one Vβ rearrangement, suggesting that replenishment of the repertoire in the adult is at least oligoclonal. These results demonstrate that the normal adult thymus continues to contribute, even in older individuals, a diverse set of new T cells to the peripheral circulation.