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T Cell Function: A Randomized, Double-Blind, Placebo-Controlled Study
Food Science and Human Nutrition Department, University of Florida (C.A.R., M.P.N., S.S.P.), Gainesville, Florida
Divison of Rheumatology, Allergy & Immunology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School (J.F.B.)
Nutritional Science Research Institute (J.F.B.), Boston, Massachusetts
Address reprint requests to: Susan S. Percival, PhD, Food Science and Human Nutrition Department, University of Florida, Gainesville, Florida 32611. E-mail: Percival{at}ufl.edu
Objective: Determine if a specific formulation of Camellia sinensis (CSF) can prevent illness and symptoms due to cold and flu, and enhance 
T cell function
Methods: Design: Randomized, double-blind, placebo-controlled study. Subjects: Healthy adults 18–70 years old. Intervention: Proprietary formulation of Camellia sinensis (green tea) capsules, or a placebo, twice a day, for 3 months. Measures of Outcome: As assessed by daily symptom logs, percentage of subjects experiencing cold and flu symptoms, number of days subjects experienced symptoms, and percentage of subjects seeking medical treatment. Mean in vivo and ex vivo proliferative and interferon gamma responses of subjects peripheral blood mononuclear cells to 
T cell antigen stimulation.
Results: Among subjects taking CSF there were 32.1% fewer subjects with symptoms (P = 0.035), 22.9% fewer overall illnesses of at least 2 days duration (P = 0.092), and 35.6% fewer symptom days (P < 0.002), compared to subjects taking placebo. 
T cells from subjects taking CSF proliferated 28% more (P = 0.017) and secreted 26% more IFN-
(P = 0.046) in response to 
T cell antigens, as compared to 
T cells from subjects taking placebo. CSF was well-tolerated.
Conclusions: This proprietary formulation of CSF is a safe and effective dietary supplement for preventing cold and flu symptoms, and for enhancing 
T cell function.
Abbreviations: CSF, Camellia sinensis formulation EGCG, epigallocatechin gallate PBMC, peripheral blood mononuclear cells IFN-
, interferon gamma
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