https://scholars.lib.ntu.edu.tw/handle/123456789/512342
標題: | High throughput sequencing of T-cell receptor repertoire using dry blood spots | 作者: | SHANG-GIN WU Pan W. Liu H. Byrne-Steele M.L. Brown B. Depinet M. Hou X. Han J. Li S. |
關鍵字: | CDR3; Diversity; Dry blood spots; Next-generation sequence; T cell receptor; TCR repertoire | 公開日期: | 2019 | 出版社: | BioMed Central Ltd. | 卷: | 17 | 期: | 1 | 起(迄)頁: | 47 | 來源出版物: | Journal of Translational Medicine | 摘要: | Background: Immunology research, particularly next generation sequencing (NGS) of the immune T-cell receptor β (TCRβ) repertoire, has advanced progression in several fields, including treatment of various cancers and autoimmune diseases. This study aimed to identify the TCR repertoires from dry blood spots (DBS), a method that will help collecting real-world data for biomarker applications. Methods: Finger-prick blood was collected onto a Whatman filter card. RNA was extracted from DBS of the filter card, and fully automated multiplex PCR was performed to generate a TCRβ chain library for next generation sequencing (NGS) analysis of unique CDR3s (uCDR3). Results: We demonstrated that the dominant clonotypes from the DBS results recapitulated those found in whole blood. According to the statistical analysis and laboratory confirmation, 40 of 2-mm punch disks from the filter cards were enough to detect the shared top clones and have strong correlation in the uCDR3 discovery with whole blood. uCDR3 discovery was neither affected by storage temperatures (room temperature versus-20 °C) nor storage durations (1, 14, and 28 days) when compared to whole blood. About 74-90% of top 50 uCDR3 clones of whole blood could also be detected from DBS. A low rate of clonotype sharing, 0.03-1.5%, was found among different individuals. Conclusions: The DBS-based TCR repertoire profiling method is minimally invasive, provides convenient sampling, and incorporates fully automated library preparation. The system is sensitive to low RNA input, and the results are highly correlated with whole blood uCDR3 discovery allowing study scale-up to better understand the relationship and mutual influences between the immune and diseases. ? 2019 The Author(s). |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85061856289&doi=10.1186%2fs12967-019-1796-4&partnerID=40&md5=6833b6ba93e5b587401361642bf82417 https://scholars.lib.ntu.edu.tw/handle/123456789/512342 |
ISSN: | 1479-5876 | DOI: | 10.1186/s12967-019-1796-4 | SDG/關鍵字: | T lymphocyte receptor beta chain; lymphocyte antigen receptor; RNA; Article; controlled study; dried blood spot testing; multiplex polymerase chain reaction; next generation sequencing; room temperature; storage temperature; complementarity determining region; dried blood spot testing; genetics; high throughput sequencing; human; isolation and purification; preservation; procedures; temperature; Complementarity Determining Regions; Dried Blood Spot Testing; High-Throughput Nucleotide Sequencing; Humans; Preservation, Biological; Receptors, Antigen, T-Cell, alpha-beta; RNA; Temperature |
顯示於: | 醫學系 |
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