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Cancer Epidemiology Biomarkers & Prevention 16, 2160-2163, October 1, 2007. doi: 10.1158/1055-9965.EPI-07-0604
© 2007 American Association for Cancer Research

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Short Communication

Cryopreservation of Whole Blood Samples Collected in the Field for a Large Epidemiologic Study

Victoria L. Stevens, Alpa V. Patel, Heather Spencer Feigelson, Carmen Rodriguez, Michael J. Thun and Eugenia E. Calle

Department of Epidemiology and Surveillance Research, American Cancer Society, Atlanta, Georgia

Requests for reprints: Victoria L. Stevens, Department of Epidemiology and Surveillance Research, American Cancer Society, 250 Williams Street, NW, Atlanta, GA 30303. Phone: 404-329-5197; Fax: 404-327-6450. E-mail: Victoria.Stevens{at}cancer.org

Cryopreserved lymphocytes can be used to measure various cellular functions and are an excellent source of DNA. However, functional studies of lymphocytes have been largely limited to specimens collected in laboratory settings because of the perception that specialized equipment and handling are needed to successfully cryopreserve biospecimens. In this study, we have developed a protocol to successfully cryopreserve blood samples collected in the field as part of a pilot study of Cancer Prevention Study-3. Blood was collected in sodium heparin–containing vacutainers at six outdoor events, transported via courier to one of four different processing labs for cryopreservation, and stored in the vapor phase of liquid nitrogen. After 2 to 6 weeks of storage, the effectiveness of the protocol was evaluated by testing 30 samples for their viability, lymphocyte yield, and ability to be transformed by EBV. Although lymphocyte recovery varied considerably, all samples yielded at least 2 x 106 cells with at least 86% of the cells being viable. All samples were successfully transformed by EBV and yielded immortalized cell lines within 15 days of treatment with the virus. These findings indicate that whole blood samples collected in the field can be successfully cryopreserved and that the normal variation in sample handling expected in a large epidemiologic study does not compromise the quality of the cryopreserved specimens. (Cancer Epidemiol Biomarkers Prev 2007;16(10):2160–3)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2007 by the American Association for Cancer Research.