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Next-generation TCR sequencing - a tool to understand T-cell infiltration in human cancers
- Source :
- The Journal of Pathology. 240:384-386
- Publication Year :
- 2016
- Publisher :
- Wiley, 2016.
-
Abstract
- Tumour-infiltrating lymphocytes (TILs) are known to mediate potent anti-tumour activity. As T-cell-based therapies start to reach clinical practice, it becomes increasingly important to understand what characterizes a successful anti-tumour T-cell response and to exploit this knowledge for patient stratification. Next-generation sequencing of T-cell receptors (TCRs) promises to provide insights into the complexity of the tumour T-cell infiltrate that go beyond the phenotypic level. A recent study by Chen et al made use of this novel technology to demonstrate that the TIL repertoire of oesophageal squamous cell carcinoma patients is distinct from that of non-tumour sites and is characterized by significant intratumoural heterogeneity. This study illustrates the great potential of the method and addresses several technical and biological hurdles that need to be considered. Careful sampling, normalization, and error correction will be required to optimally use TCR sequencing to answer biological questions and define predictive biomarkers, e.g. for cancer immunotherapy. Copyright © 2016 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
- Subjects :
- 0301 basic medicine
Tumor-infiltrating lymphocytes
T-Lymphocytes
medicine.medical_treatment
Repertoire
T-cell receptor
T cell infiltration
High-Throughput Nucleotide Sequencing
Biology
Bioinformatics
United Kingdom
DNA sequencing
Pathology and Forensic Medicine
Clinical Practice
03 medical and health sciences
Lymphocytes, Tumor-Infiltrating
030104 developmental biology
0302 clinical medicine
Cancer immunotherapy
030220 oncology & carcinogenesis
medicine
Humans
Predictive biomarker
Subjects
Details
- ISSN :
- 00223417
- Volume :
- 240
- Database :
- OpenAIRE
- Journal :
- The Journal of Pathology
- Accession number :
- edsair.doi.dedup.....170d25593f3e1dde2e58b504a5f62cba
- Full Text :
- https://doi.org/10.1002/path.4800