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T lymphocytes in aged people and centenarians

* Laboratory of Tumor Immunology, Immunology Center, INRCA Gerontol. Res. Dept., Ancona, Italy; and
Department of Experimental Pathology, University of Bologna, Italy
Correspondence: Mauro Provinciali, M.D., Laboratory of Tumor Immunology, Immunology Center, INRCA Gerontol. Res. Dept., Via Birarelli 8, 60121 Ancona, Italy. E-mail: m.provinciali{at}inrca.it
The aim of this study was to evaluate the peripheral representation, in vitro expansion, cytokine production, and cytotoxicity of 
T lymphocytes from 104 healthy subjects ranging in age from 19 to 103 years. We demonstrated that the absolute number of circulating 
+ T cells was reduced significantly in old people and centenarians in comparison with young subjects as a consequence of the age-related decreased lymphocyte number. The decrease was a result of an age-dependent reduction of V
2 T cells, whereas the absolute number of V
1 T cells was unaffected by age. As a consequence, the V
2/V
1 ratio was inverted in old subjects and centenarians. A higher percentage of 
+ T cells producing tumor necrosis factor
was found in old donors and centenarians, whereas no age-related difference was observed in interferon -
production. After a 10-day in vitro expansion, a twofold lower expansion index of 
T cells, and particularly of a V
2, but not of a V
1 subset, was found in old people and centenarians in comparison with young subjects. The cytotoxicity of sorted 
T cells was preserved in old people and centenarians. The alteration of 
T cells could contribute to the age-related derangement of T cell-mediated, adoptive responses and may represent a new characteristic of immunosenescence.
Key Words: aging human cellular activation cytotoxicity
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