| Literature DB >> 29895573 |
Ludmila Danilova1,2,3, Valsamo Anagnostou1,2, Franck Housseau1,2, Kellie N Smith4,2, Justina X Caushi1,2, John-William Sidhom1,2, Haidan Guo1,2, Hok Yee Chan1,2, Prerna Suri1,2, Ada Tam1,2, Jiajia Zhang1,2, Margueritta El Asmar1,2, Kristen A Marrone1,2, Jarushka Naidoo1,2, Julie R Brahmer1,2, Patrick M Forde1,2, Alexander S Baras1,2,5, Leslie Cope1,2, Victor E Velculescu1,2, Drew M Pardoll1,2.
Abstract
Mutation-associated neoantigens (MANA) are a target of antitumor T-cell immunity. Sensitive, simple, and standardized assays are needed to assess the repertoire of functional MANA-specific T cells in oncology. Assays analyzing in vitro cytokine production such as ELISpot and intracellular cytokine staining have been useful but have limited sensitivity in assessing tumor-specific T-cell responses and do not analyze antigen-specific T-cell repertoires. The FEST (Functional Expansion of Specific T cells) assay described herein integrates T-cell receptor sequencing of short-term, peptide-stimulated cultures with a bioinformatic platform to identify antigen-specific clonotypic amplifications. This assay can be adapted for all types of antigens, including MANAs via tumor exome-guided prediction of MANAs. Following in vitro identification by the MANAFEST assay, the MANA-specific CDR3 sequence can be used as a molecular barcode to detect and monitor the dynamics of these clonotypes in blood, tumor, and normal tissue of patients receiving immunotherapy. MANAFEST is compatible with high-throughput routine clinical and lab practices. Cancer Immunol Res; 6(8); 888-99. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 29895573 PMCID: PMC6072595 DOI: 10.1158/2326-6066.CIR-18-0129
Source DB: PubMed Journal: Cancer Immunol Res ISSN: 2326-6066 Impact factor: 11.151