Decreased proliferative capacity and increased susceptibility to activation-induced cell death in late-passage human cd4 + tcr2 + cultured T cell clones

• Published in: Experimental gerontology Vol. 31; no. 6; pp. 655 - 668
• Main Authors: Pawelec, Graham, Sansom, David, Rehbein, Arnika, Adibzadeh, Medi, Beckman, Ian
• Format: Journal Article
• Language: English
• Published: England Elsevier Inc 01.11.1996
• Subjects: activation-induced cell death; Animals; Antigen-Presenting Cells - physiology; CD28; CD4 Antigens - analysis; Cellular Senescence; CHO Cells; costimulation; Cricetinae; Cytokines - pharmacology; Humans; Immunophenotyping; immunosenescence; Lymphocyte Activation; Receptors, Antigen, T-Cell - analysis; T lymphocyte aging; T lymphocyte clones; T lymphocyte proliferation; T-Lymphocytes - physiology; activation-induced cell death; immunosenescence; costimulation; T lymphocyte aging; CD28; T lymphocyte proliferation; T lymphocyte clones
• ISSN: 0531-5565; 1873-6815
• DOI: 10.1016/S0531-5565(96)00097-6

The growth characteristics in vitro of interleukin 2 (IL 2)-dependent human CD4 + αβ-T cell receptor-positive helper T cell clones (TCC) were studied in relation to alterations in surface phenotype, cytokine responsiveness, and susceptibility to activation-induced cell death (AICD). TCC derived from peripheral blood T cells had finite lifespans averaging 33 population doublings (PD) with a recorded maximum lifespan of 80 PD ( n = 208). First analyses of the TCC were undertaken at ca. 25 PD, at which time all cells of all TCC expressed high intensity CD45RO and low intensity CD45RA, as well as high intensity CD95 (fas) and MHC class II antigens. The expression of these molecules remained elevated throughout the proliferative lifespan of the clones, but for those TCC which were initially CD28 + (the majority), the density of expression of the latter was diminished in most late-passage clones. Concomitant with this, late-passage cells showed reduced responsiveness to CD28-mediated costimulation by CHO transfectants expressing human CD80 compared to early-passage cells. Additionally, the level of expression of IL 2Rγc and IL 7R chains was commonly reduced, as was the response to IL 2 and IL 7. Despite unchanged levels of fas expression on TCC with time, late-passage cells were more susceptible to AICD than early-passage cells. These observations further document functional and phenotypic alterations in long-term cultured human T helper cells, which may be considered as biomarkers of immunosenescence. This may contribute to an improved understanding of the mechanisms underlying depressed T cell function in old age.