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10.3390/ijms21218324

http://scihub22266oqcxt.onion/10.3390/ijms21218324
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33171940!7664211!33171940
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suck abstract from ncbi

pmid33171940      Int+J+Mol+Sci 2020 ; 21 (21): ?
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  • Needle in a Haystack: The Naive Repertoire as a Source of T Cell Receptors for Adoptive Therapy with Engineered T Cells #MMPMID33171940
  • D'Ippolito E; Wagner KI; Busch DH
  • Int J Mol Sci 2020[Nov]; 21 (21): ? PMID33171940show ga
  • T cell engineering with antigen-specific T cell receptors (TCRs) has allowed the generation of increasingly specific, reliable, and versatile T cell products with near-physiological features. However, a broad applicability of TCR-based therapies in cancer is still limited by the restricted number of TCRs, often also of suboptimal potency, available for clinical use. In addition, targeting of tumor neoantigens with TCR-engineered T cell therapy moves the field towards a highly personalized treatment, as tumor neoantigens derive from somatic mutations and are extremely patient-specific. Therefore, relevant TCRs have to be de novo identified for each patient and within a narrow time window. The naive repertoire of healthy donors would represent a reliable source due to its huge diverse TCR repertoire, which theoretically entails T cells for any antigen specificity, including tumor neoantigens. As a challenge, antigen-specific naive T cells are of extremely low frequency and mostly of low functionality, making the identification of highly functional TCRs finding a "needle in a haystack." In this review, we present the technological advancements achieved in high-throughput mapping of patient-specific neoantigens and corresponding cognate TCRs and how these platforms can be used to interrogate the naive repertoire for a fast and efficient identification of rare but therapeutically valuable TCRs for personalized adoptive T cell therapy.
  • |Antigens, Neoplasm/genetics[MESH]
  • |CD4-Positive T-Lymphocytes/immunology[MESH]
  • |CD8-Positive T-Lymphocytes/immunology[MESH]
  • |Humans[MESH]
  • |Immunotherapy, Adoptive/*methods/trends[MESH]
  • |Neoplasms/genetics[MESH]
  • |Precision Medicine/methods[MESH]
  • |Receptors, Antigen, T-Cell/*genetics/*metabolism/physiology[MESH]


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