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PMID: 21945395 Published · ppublish English Journal Article

Ultra-sensitive detection of rare T cell clones.

Journal of immunological methods ·Vol. 375 ·No. 1-2 ·2012-01-31 ·Pages 14-9

Robins H, Desmarais C, Matthis J, Livingston R, Andriesen J, Reijonen H, Carlson C, Nepom G, Yee C, Cerosaletti K

Abstract

Advances in high-throughput sequencing have enabled technologies that probe the adaptive immune system with unprecedented depth. We have developed a multiplex PCR method to sequence tens of millions of T cell receptors (TCRs) from a single sample in a few days. A method is presented to test the precision, accuracy, and sensitivity of this assay. T cell clones, each with one fixed productive TCR rearrangement, are doped into complex blood cell samples. TCRs from a total of eleven samples are sequenced, with the doped T cell clones ranging from 10% of the total sample to 0.001% (one cell in 100,000). The assay is able to detect even the rarest clones. The precision of the assay is demonstrated across five orders of magnitude. The accuracy for each clone is within an overall factor of three across the 100,000 fold dynamic range. Additionally, the assay is shown to be highly repeatable.

MeSH Terms
Clone Cells High-Throughput Nucleotide Sequencing/methods Humans Multiplex Polymerase Chain Reaction/methods Receptors, Antigen, T-Cell/genetics Reproducibility of Results Sensitivity and Specificity
Chemicals
Receptors, Antigen, T-Cell
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Robins Harlan
Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States. hrobins@fhcrc.org
Desmarais Cindy
Matthis Jessica
Livingston Robert
Andriesen Jessica
Reijonen Helena
Carlson Christopher
Nepom Gerold
Yee Cassian
Cerosaletti Karen
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Article Info
Journal
Journal of immunological methods
Abbr.
J Immunol Methods
ISSN
1872-7905
Published
2012-01-31
Epub
2011-00-10
Pages
14-9
Language
English
Region
Netherlands
NLM ID
1305440
PMCID
PMC3721519
Subset
IM
Grants
NIDDK NIH HHS · R43 DK089783 · United States
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