Advances in identification and selection of personalized neoantigen/T-cell pairs for autologous adoptive T cell therapies

Oncoimmunology. 2021 Jan 7;10(1):1869389. doi: 10.1080/2162402X.2020.1869389.

Abstract

Based on the success of tumor-infiltrating lymphocytes (TIL)-based therapies, personalized adoptive cell therapies (ACT) targeting neoantigens have the potential to become a disruptive technology and lead to highly effective treatments for cancer patients for whom no other options exist. ACT of TIL, peripheral blood or gene-engineered peripheral blood lymphocytes (PBLs) targeting neoantigens is a highly personalized intervention that requires three discrete steps: i) Identification of suitable personal targets (neoantigens), ii) selection of T cells or their T cell receptors (TCRs) that are specific for the identified neoantigens and iii) expansion of the selected T cell population or generation of sufficient number of TCR modified T cells. In this review, we provide an introduction into challenges and approaches to identify neoantigens and to select the Adoptive Cell Therapy, ACT, Neoantigen, T cell, Cancer respective neoantigen-reactive T cells for use in ACT.

Keywords: ACT; Adoptive Cell Therapy; Cancer; Neoantigen; T cell.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antigens, Neoplasm / genetics
  • Humans
  • Immunotherapy, Adoptive
  • Lymphocytes, Tumor-Infiltrating*
  • Receptors, Antigen, T-Cell / genetics
  • T-Lymphocytes*

Substances

  • Antigens, Neoplasm
  • Receptors, Antigen, T-Cell