In vivo reduction of telomere length in human antigen‐reactive memory T cells

• Published in: European journal of immunology Vol. 30; no. 7; pp. 1894 - 1901
• Main Authors: Burns, James B., Lobo, Stephen T., Bartholomew, Breck D.
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY‐VCH Verlag GmbH 01.07.2000
• Subjects: Adult; Candida albicans - immunology; CD4-Positive T-Lymphocytes - cytology; CD4-Positive T-Lymphocytes - immunology; Cells, Cultured; Flow Cytometry - methods; Human; Humans; Immunologic Memory - immunology; In Situ Hybridization - methods; Leukocyte Common Antigens - immunology; Memory T cell; Middle Aged; T lymphocyte; Telomere; Tetanus Toxoid - immunology
• ISSN: 0014-2980; 1521-4141
• DOI: 10.1002/1521-4141(200007)30:7<1894::AID-IMMU1894>3.0.CO;2-N

There is a reduction in the average telomere lengths of CD4+ "memory" T cells, defined by the CD45RO+ phenotype, compared to CD54RA+ "naive" T cells. However, other studies suggest that telomerase activity often is sufficient to maintain the telomere length of certain B and T cell populations following immune activation in vivo. Thus it is uncertain whether genuine memory CD4+ T cells, defined by an immune response to specific recall antigens, would display telomeres of reduced length, or whether telomere size would be maintained. Therefore, we examined the telomere lengths of T cells responding to two common recall antigens, tetanus toxoid and Candida albicans. Telomere terminal restriction fragment length was assessed by Southern blots or by flow cytometry following in situ hybridization with telomere‐specific peptide nucleic acid probes. For the five subjects tested, the Candida‐ or tetanus‐reactive memory T cell populations demonstrated a significant reduction of telomere length even when compared to the phenotypically defined memory CD45RO+ T cell populations isolated from peripheral blood mononuclear cells. This finding suggests that telomerase activity does not fully compensate for the effects of in vivo activation and proliferation of some antigen‐specific CD4+ T cell populations. This may contribute to immune senescence.