» Articles » PMID: 36059451

CAR-T Cell Development for Cutaneous T Cell Lymphoma: Current Limitations and Potential Treatment Strategies

Overview
Journal Front Immunol
Date 2022 Sep 5
PMID 36059451
Authors
Affiliations
Soon will be listed here.
Abstract

Chimeric antigen receptor (CAR)-T therapy has demonstrated remarkable outcomes for B cell malignancies, however, its application for T cell lymphoma, particularly cutaneous T cell lymphoma (CTCL), has been limited. Barriers to effective CAR-T cell therapy in treating CTCL include T cell aplasia in autologous transplants, CAR-T product contamination with leukemic T cells, CAR-T fratricide (when the target antigen is present on normal T cells), and tumor heterogeneity. To address these critical challenges, innovative CAR engineering by targeting multiple antigens to strike a balance between efficacy and safety of the therapy is necessary. In this review, we discuss the current obstacles to CAR-T cell therapy and highlight potential targets in treating CTCL. Looking forward, we propose strategies to develop more powerful dual CARs that are advancing towards the clinic in CTCL therapy.

Citing Articles

Unveiling the Role of the Cellular Tumor Microenvironment and the Therapeutic Targets it Provides in Cutaneous T-Cell Lymphoma.

Chinas N, Kaliampou S, Nikolaou V Curr Oncol Rep. 2025; .

PMID: 40055269 DOI: 10.1007/s11912-025-01646-6.


Advances in Novel Systemic Therapies for the Management of Cutaneous T Cell Lymphoma (CTCL).

Case K, Allen P Curr Hematol Malig Rep. 2025; 20(1):5.

PMID: 39800801 DOI: 10.1007/s11899-024-00746-7.


T-cell receptor architecture and clonal tiding provide insight into the transformation trajectory of peripheral T-cell lymphomas.

Willscher E, Schultheiss C, Paschold L, Lea Schumann F, Schmidt-Barbo P, Thiele B Haematologica. 2024; 110(2):457-469.

PMID: 39219501 PMC: 11788643. DOI: 10.3324/haematol.2024.285395.


The potential role of CD8+ cytotoxic T lymphocytes and one branch connected with tissue-resident memory in non-luminal breast cancer.

Zhao Z, Ma X, Cai Z PeerJ. 2024; 12:e17667.

PMID: 39006029 PMC: 11246025. DOI: 10.7717/peerj.17667.


Immune landscape and response to oncolytic virus-based immunotherapy.

Lin C, Teng W, Tian Y, Li S, Xia N, Huang C Front Med. 2024; 18(3):411-429.

PMID: 38453818 DOI: 10.1007/s11684-023-1048-0.


References
1.
Hege K, Bergsland E, Fisher G, Nemunaitis J, Warren R, McArthur J . Safety, tumor trafficking and immunogenicity of chimeric antigen receptor (CAR)-T cells specific for TAG-72 in colorectal cancer. J Immunother Cancer. 2017; 5:22. PMC: 5360066. DOI: 10.1186/s40425-017-0222-9. View

2.
Nicolet C, Siegel D, Surfus J, Sondel P . TAG-72-reactive antibody CC49 recognizes molecules expressed by hematopoietic cell lines. Tumour Biol. 1997; 18(6):356-66. DOI: 10.1159/000218050. View

3.
Ruella M, Xu J, Barrett D, Fraietta J, Reich T, Ambrose D . Induction of resistance to chimeric antigen receptor T cell therapy by transduction of a single leukemic B cell. Nat Med. 2018; 24(10):1499-1503. PMC: 6511988. DOI: 10.1038/s41591-018-0201-9. View

4.
Sotillo E, Barrett D, Black K, Bagashev A, Oldridge D, Wu G . Convergence of Acquired Mutations and Alternative Splicing of CD19 Enables Resistance to CART-19 Immunotherapy. Cancer Discov. 2015; 5(12):1282-95. PMC: 4670800. DOI: 10.1158/2159-8290.CD-15-1020. View

5.
Duarte R, Canals C, Onida F, Gabriel I, Arranz R, Arcese W . Allogeneic hematopoietic cell transplantation for patients with mycosis fungoides and Sézary syndrome: a retrospective analysis of the Lymphoma Working Party of the European Group for Blood and Marrow Transplantation. J Clin Oncol. 2010; 28(29):4492-9. DOI: 10.1200/JCO.2010.29.3241. View