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TCR mimic compounds for pHLA targeting with high potency modalities in oncology
pHLA complexes represent the largest class of cell surface markers on cancer cells, making them attractive for targeted cancer therapies. Adoptive cell therapies expressing TCRs that recognize tumor specific pHLAs take advantage of the unique selectivity and avidity of TCR: pHLA interactions. More r...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635445/ https://www.ncbi.nlm.nih.gov/pubmed/36338746 http://dx.doi.org/10.3389/fonc.2022.1027548 |
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author | Gerber, Hans-Peter Presta, Leonard G. |
author_facet | Gerber, Hans-Peter Presta, Leonard G. |
author_sort | Gerber, Hans-Peter |
collection | PubMed |
description | pHLA complexes represent the largest class of cell surface markers on cancer cells, making them attractive for targeted cancer therapies. Adoptive cell therapies expressing TCRs that recognize tumor specific pHLAs take advantage of the unique selectivity and avidity of TCR: pHLA interactions. More recently, additional protein binding domains binding to pHLAs, known as TCR mimics (TCRm), were developed for tumor targeting of high potency therapeutic modalities, including bispecifics, ADCs, CAR T and -NK cells. TCRm compounds take advantage of the exquisite tumor specificity of certain pHLA targets, including cell lineage commitment markers and cancer testis antigens (CTAs). To achieve meaningful anti-tumor responses, it is critical that TCRm compounds integrate both, high target binding affinities and a high degree of target specificity. In this review, we describe the most advanced approaches to achieve both criteria, including affinity- and specificity engineering of TCRs, antibodies and alternative protein scaffolds. We also discuss the status of current TCRm based therapeutics developed in the clinic, key challenges, and emerging trends to improve treatment options for cancer patients treated with TCRm based therapeutics in Oncology. |
format | Online Article Text |
id | pubmed-9635445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96354452022-11-05 TCR mimic compounds for pHLA targeting with high potency modalities in oncology Gerber, Hans-Peter Presta, Leonard G. Front Oncol Oncology pHLA complexes represent the largest class of cell surface markers on cancer cells, making them attractive for targeted cancer therapies. Adoptive cell therapies expressing TCRs that recognize tumor specific pHLAs take advantage of the unique selectivity and avidity of TCR: pHLA interactions. More recently, additional protein binding domains binding to pHLAs, known as TCR mimics (TCRm), were developed for tumor targeting of high potency therapeutic modalities, including bispecifics, ADCs, CAR T and -NK cells. TCRm compounds take advantage of the exquisite tumor specificity of certain pHLA targets, including cell lineage commitment markers and cancer testis antigens (CTAs). To achieve meaningful anti-tumor responses, it is critical that TCRm compounds integrate both, high target binding affinities and a high degree of target specificity. In this review, we describe the most advanced approaches to achieve both criteria, including affinity- and specificity engineering of TCRs, antibodies and alternative protein scaffolds. We also discuss the status of current TCRm based therapeutics developed in the clinic, key challenges, and emerging trends to improve treatment options for cancer patients treated with TCRm based therapeutics in Oncology. Frontiers Media S.A. 2022-10-21 /pmc/articles/PMC9635445/ /pubmed/36338746 http://dx.doi.org/10.3389/fonc.2022.1027548 Text en Copyright © 2022 Gerber and Presta https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Gerber, Hans-Peter Presta, Leonard G. TCR mimic compounds for pHLA targeting with high potency modalities in oncology |
title | TCR mimic compounds for pHLA targeting with high potency modalities in oncology |
title_full | TCR mimic compounds for pHLA targeting with high potency modalities in oncology |
title_fullStr | TCR mimic compounds for pHLA targeting with high potency modalities in oncology |
title_full_unstemmed | TCR mimic compounds for pHLA targeting with high potency modalities in oncology |
title_short | TCR mimic compounds for pHLA targeting with high potency modalities in oncology |
title_sort | tcr mimic compounds for phla targeting with high potency modalities in oncology |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635445/ https://www.ncbi.nlm.nih.gov/pubmed/36338746 http://dx.doi.org/10.3389/fonc.2022.1027548 |
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