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T-lymphocytes expressing CC chemokine receptor-5 are increased in frail older adults.

作者信息

De Fanis Umberto, Wang George C, Fedarko Neal S, Walston Jeremy D, Casolaro Vincenzo, Leng Sean X

机构信息

Division of Allergy and Clinical Immunology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224, USA.

出版信息

J Am Geriatr Soc. 2008 May;56(5):904-8. doi: 10.1111/j.1532-5415.2008.01673.x. Epub 2008 Apr 1.

Abstract

OBJECTIVES

To evaluate the frequencies of T-lymphocytes expressing CC chemokine receptor-5 (CCR5(+) T-cells) and their relationship with frailty in older adults.

DESIGN

Case-control study with an age-, race-, and sex-matched design.

SETTING

General Clinical Research Center.

PARTICIPANTS

Community-dwelling adults aged 72 and older from Baltimore, Maryland.

METHODS

Frailty was determined using five validated criteria: weakness, slow walking speed, fatigue, low physical activity, and weight loss. Those meeting three or more of these five criteria were defined as frail and those with none as nonfrail. Complete blood counts were performed to obtain peripheral lymphocyte counts using an automated (Coulter) counter. Peripheral blood was collected for surface immunofluorescent staining of CCR5 and other T-cell markers.

RESULTS

Twenty-six frail and matched nonfrail participants (mean age+/-standard deviation 83.8+/-5.3, range 72-94) completed the study. Frail participants had higher CCR5(+), CCR5(+)CD8(+), and CCR5(+)CD45RO(-) T-cell counts than matched nonfrail controls (349+/-160/mm(3) vs 194+/-168/mm(3), P=.02; 208+/-98/mm(3) vs 105+/-62/mm(3), P=.02; and 189+/-149/mm(3) vs 52+/-36/mm(3), P=.01; respectively). Furthermore, there was a trend toward graded increase in these T-cell counts across the frailty scores in frail participants (e.g., CCR5(+)CD8(+) counts of 123+/-52/mm(3), 248+/-115/mm(3), and 360+/-215/mm(3) for those with frailty scores of 3, 4, and 5, respectively).

CONCLUSION

These initial results suggest an expansion of the CCR5(+) T-cell subpopulation in frailty. They provide a basis for further characterization of CCR5(+) T-cells and their role in frailty, with potential therapeutic implications.

摘要

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