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Clinical and Diagnostic Laboratory Immunology, July 2002, p. 858-863, Vol. 9, No. 4
1071-412X/02/$04.00+0 DOI: 10.1128/CDLI.9.4.858-863.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
and Beth D. Jamieson2
Department of Epidemiology,1 Department of Medicine and Jonsson Comprehensive Cancer Center, and,2 Department of Biostatistics,University of California, Los Angeles, California3
Received 14 November 2001/ Returned for modification 29 January 2002/ Accepted 10 April 2002
T-cell receptor diversity enables the cellular immune response to recognize a broad range of viral and other pathogenic agents. An increasingly common method of characterizing T-cell receptor diversity and usage in response to antigenic challenges involves the identification of clonal expansions by PCR amplification of the CDR3 region of distinct TCRVß families. Though clonal expansions often appear evident upon visual inspection of the results, a systematic method is needed for the valid enumeration of these expansions. Here, we describe a novel analysis method, termed the MaGiK method, for systematically identifying and enumerating clonal T-cell expansions and for applying the results to investigations of the T-cell receptor repertoire.
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