» Articles » PMID: 33362790

Paving the Way Towards Universal Chimeric Antigen Receptor Therapy in Cancer Treatment: Current Landscape and Progress

Overview
Journal Front Immunol
Date 2020 Dec 28
PMID 33362790
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Chimeric antigen receptor (CAR) therapy has been proved effective in a stream of clinical trials, especially in hematologic malignancies. However, current CAR therapy is highly personalized as cells used are derived from patients themselves, which can be costly, time-consuming, and sometimes fails to achieve optimal therapeutic results due to poor quality/quantity of patient-derived cells. On the contrary, universal CAR therapy, which is based on healthy individuals' cells, circumvents several limitations of current autologous CAR therapy. To achieve the universality of CAR therapy, the allogeneic cell transplantation related issues, such as graft--host disease (GVHD) and host--graft activities (HVGA), must be addressed. In this review, we focus on current progress regarding GVHD and HVGA in the universal CAR therapy, followed by a universal CAR design that may be applied to allogeneic cells and a summary of key clinical trials in this field. This review may provide valuable insights into the future design of universal CAR products.

Citing Articles

CAR-NK cells in combination therapy against cancer: A potential paradigm.

Li J, Hu H, Lian K, Zhang D, Hu P, He Z Heliyon. 2024; 10(5):e27196.

PMID: 38486782 PMC: 10937699. DOI: 10.1016/j.heliyon.2024.e27196.


CAR and CAR T cells share a differentiation trajectory into an NK-like subset after CD19 CAR T cell infusion in patients with B cell malignancies.

Louie R, Cai C, Samir J, Singh M, Deveson I, Ferguson J Nat Commun. 2023; 14(1):7767.

PMID: 38012187 PMC: 10682404. DOI: 10.1038/s41467-023-43656-7.


New cell sources for CAR-based immunotherapy.

Mazinani M, Rahbarizadeh F Biomark Res. 2023; 11(1):49.

PMID: 37147740 PMC: 10163725. DOI: 10.1186/s40364-023-00482-9.


Antiviral Cell Products against COVID-19: Learning Lessons from Previous Research in Anti-Infective Cell-Based Agents.

Chikileva I, Shubina I, Burtseva A, Kirgizov K, Stepanyan N, Varfolomeeva S Biomedicines. 2022; 10(4).

PMID: 35453618 PMC: 9027720. DOI: 10.3390/biomedicines10040868.

References
1.
Netea M, Latz E, Mills K, ONeill L . Innate immune memory: a paradigm shift in understanding host defense. Nat Immunol. 2015; 16(7):675-9. DOI: 10.1038/ni.3178. View

2.
Barber A, Rynda A, Sentman C . Chimeric NKG2D expressing T cells eliminate immunosuppression and activate immunity within the ovarian tumor microenvironment. J Immunol. 2009; 183(11):6939-47. PMC: 2825039. DOI: 10.4049/jimmunol.0902000. View

3.
Boch J, Scholze H, Schornack S, Landgraf A, Hahn S, Kay S . Breaking the code of DNA binding specificity of TAL-type III effectors. Science. 2009; 326(5959):1509-12. DOI: 10.1126/science.1178811. View

4.
Ghosh A, Smith M, James S, Davila M, Velardi E, Argyropoulos K . Donor CD19 CAR T cells exert potent graft-versus-lymphoma activity with diminished graft-versus-host activity. Nat Med. 2017; 23(2):242-249. PMC: 5528161. DOI: 10.1038/nm.4258. View

5.
Koch J, Steinle A, Watzl C, Mandelboim O . Activating natural cytotoxicity receptors of natural killer cells in cancer and infection. Trends Immunol. 2013; 34(4):182-91. DOI: 10.1016/j.it.2013.01.003. View