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Clinical and Diagnostic Laboratory Immunology, March 2000, p. 307-311, Vol. 7, No. 2
Cylex Inc., Columbia, Maryland
210451; ImmTech, Inc., New Windsor,
Maryland 217622; and U.S. Department
of Agriculture, Little Rock, Arkansas 722113
Received 19 July 1999/Returned for modification 18 October
1999/Accepted 14 December 1999
The proliferative response is most frequently determined by
estimating the amount of [3H]thymidine incorporated into
newly synthesized DNA. The [3H]thymidine procedure
requires the use of radioisotopes as well as lengthy periods of
incubation (>72 h). An alternative method of assessing T-lymphocyte
activation in whole-blood cultures involves the measurement of the
nucleotide ATP instead of [3H]thymidine incorporation. In
addition, the Luminetics assay of T-cell activation measures specific
T-lymphocyte subset responses through the use of paramagnetic particles
coated with monoclonal antibodies against CD antigens. This assay
permits rapid (24 h) analysis of lymphocyte subset activation responses
to mitogens and recall antigens in small amounts of blood.
1071-412X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Measurement of T-Lymphocyte Responses in
Whole-Blood Cultures Using Newly Synthesized DNA and ATP
*
Corresponding author. Mailing address: Cylex Inc., 8970 Old Annapolis Rd., Columbia, MD 21045. Phone: (410) 964-0236. Fax: (410) 964-0367. E-mail: contact{at}cyclex.net.
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