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Challenges and solutions for therapeutic TCR-based agents.
Malviya, Manish; Aretz, Zita E H; Molvi, Zaki; Lee, Jayop; Pierre, Stephanie; Wallisch, Patrick; Dao, Tao; Scheinberg, David A.
  • Malviya M; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Aretz ZEH; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Molvi Z; Physiology, Biophysics & Systems Biology Program, Weill Cornell Graduate School of Medical Sciences, New York City, New York, USA.
  • Lee J; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Pierre S; Physiology, Biophysics & Systems Biology Program, Weill Cornell Graduate School of Medical Sciences, New York City, New York, USA.
  • Wallisch P; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Dao T; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Scheinberg DA; Weill-Cornell Medicine, Rockefeller University, Sloan Kettering Institute, Medical Scientist Training Program, New York City, New York, USA.
Immunol Rev ; 320(1): 58-82, 2023 Nov.
Article en En | MEDLINE | ID: mdl-37455333
ABSTRACT
Recent development of methods to discover and engineer therapeutic T-cell receptors (TCRs) or antibody mimics of TCRs, and to understand their immunology and pharmacology, lag two decades behind therapeutic antibodies. Yet we have every expectation that TCR-based agents will be similarly important contributors to the treatment of a variety of medical conditions, especially cancers. TCR engineered cells, soluble TCRs and their derivatives, TCR-mimic antibodies, and TCR-based CAR T cells promise the possibility of highly specific drugs that can expand the scope of immunologic agents to recognize intracellular targets, including mutated proteins and undruggable transcription factors, not accessible by traditional antibodies. Hurdles exist regarding discovery, specificity, pharmacokinetics, and best modality of use that will need to be overcome before the full potential of TCR-based agents is achieved. HLA restriction may limit each agent to patient subpopulations and off-target reactivities remain important barriers to widespread development and use of these new agents. In this review we discuss the unique opportunities for these new classes of drugs, describe their unique antigenic targets, compare them to traditional antibody therapeutics and CAR T cells, and review the various obstacles that must be overcome before full application of these drugs can be realized.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptores de Antígenos de Linfocitos T / Neoplasias Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptores de Antígenos de Linfocitos T / Neoplasias Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article