4.8 Article

Single-cell genomic approaches for developing the next generation of immunotherapies

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NATURE MEDICINE
卷 26, 期 2, 页码 171-177

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41591-019-0736-4

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资金

  1. Cancer Research Institute
  2. Chan Zuckerberg Initiative
  3. HHMI International Scholar award
  4. Merck KGaA, Darmstadt, Germany
  5. European Research Council Consolidator Grant (ERC-COG) [724471-HemTree2.0]
  6. Thompson Family Foundation
  7. MRA Established Investigator Award [509044]
  8. Eden and Steven Romick Professorial Chair and Eden and Steven Romick Post-Doctoral Fellowship Fund
  9. Israel Science Foundation [703/15]
  10. Ernest and Bonnie Beutler Research Program for Excellence in Genomic Medicine
  11. Helen and Martin Kimmel award for innovative investigation
  12. NeuroMac DFG/Transregional Collaborative Research Center Grant
  13. International Progressive MS Alliance/NMSS [PA-1604-08459]
  14. Adelis Foundation grant
  15. Teva Pharmaceutical Industries research grant
  16. Rising Tide Translation Cancer Research Fund
  17. Melanoma Research Alliance (MRA) Young Investigator Award
  18. Israel Cancer Research Fund (ICRF) Research Career Development Award
  19. Israel Cancer Association Research Grant
  20. Mizutani Foundation for Glycoscience
  21. Emerson Collective Cancer Research Fund
  22. Israel Science Foundation (ISF) Individual Research Grant
  23. Moross Integrated Cancer Center, a Harry J. Lloyd Trust Career Development Award
  24. Flight Attendant Medical Research Institute (FAMRI) Research Grants
  25. Ira and Diana Riklis Fund for CAR-T Therapy
  26. Enoch Foundation
  27. Pearl Welinsky Merlo Foundation
  28. Benoziyo Fund for the Advancement of Science
  29. Gerty Schwarz Schaier

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Recent progress in single-cell genomics urges its application in drug development, particularly of cancer immunotherapies. Current immunotherapy pipelines are focused on functional outcome and simple cellular and molecular readouts. A thorough mechanistic understanding of the cells and pathways targeted by immunotherapy agents is lacking, which limits the success rate of clinical trials. A large leap forward can be made if the immunotherapy target cells and pathways are characterized at high resolution before and after treatment, in clinical cohorts and model systems. This will enable rapid development of effective immunotherapies and data-driven design of synergistic drug combinations. In this Perspective, we discuss how emerging single-cell genomic technologies can serve as an engine for target identification and drug development. Amit and colleagues discuss where single-cell genomic technologies can be applied both in trial design and in the clinical trial stage to improve the development of immunotherapies.

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