Keywords :
Adolescent; Adult; Aged; Aged, 80 and over; Aging/immunology; Cell Differentiation/immunology; Child; Gene Rearrangement, T-Lymphocyte/genetics; Graft vs Host Disease/immunology; Hematopoietic Stem Cell Transplantation; Homeostasis/immunology; Humans; Immunologic Memory/immunology; Lymphopoiesis/immunology; Middle Aged; Neurosecretory Systems/immunology; Receptors, Antigen, T-Cell/genetics; Recombination, Genetic/genetics; T-Lymphocytes/immunology; Thymus Gland/immunology; Transplantation Immunology/immunology
Abstract :
[en] In the precedent article, we have described how T-cell generation in the thymus (thymopoiesis) may be currently evaluated through quantification by PCR of T-cell receptor excision circles (TREC) generated by intrathymic random recombination of the gene segments coding for variable parts of T-cell receptor for antigen (TCR). In hematology, TREC methodology helps in a better understanding of immune reconstitution after graft of hematopoietic stem cells: first there is a proliferation of mature T cells present in the graft, then a differentiation of naive T cells. In geriatrics, the homeostasis of the peripheral T-cell repertoire is maintained through proliferation of peripheral memory T cells rather than through thymic generation of naive T cells. In addition, TREC quantification constitutes a novel major tool for deciphering the tight control of thymopoiesis by the neuroendocrine system.
Scopus citations®
without self-citations
2