Immune checkpoint inhibitors and cellular treatment for lymphoma immunotherapy
- PMID: 33675535
- PMCID: PMC8209615
- DOI: 10.1111/cei.13592
Immune checkpoint inhibitors and cellular treatment for lymphoma immunotherapy
Abstract
Malignant lymphoma (ML) is a common hematological malignancy with many subtypes. Patients with ML usually undergo traditional treatment failure and become relapsed or refractory (R/R) cases. Recently, immunotherapy, such as immune checkpoint inhibitors (ICIs) and cellular treatment, has gradually emerged and used in clinical trials with encouraging achievements for ML treatment, which exerts anti-tumor activity by blocking the immune evasion of tumor cells and enhancing the attack ability of immune cells. Targets of immune checkpoints include programmed cell death-1 (PD-1), programmed cell death-ligand 1 (PD-L1), cytotoxic T lymphocyte-associated protein 4 (CTLA-4), T cell immunoglobulin and ITIM domain (TIGIT), T cell immunoglobulin-3 (TIM-3) and lymphocyte activation gene 3 (LAG-3). Examples of cellular treatment are chimeric antigen receptor (CAR) T cells, cytokine-induced killer (CIK) cells and natural killer (NK) cells. This review aimed to present the current progress and future prospects of immunotherapy in lymphoma, with the focus upon ICIs and cellular treatment.
Keywords: cell therapy; clinical trials; immune checkpoint inhibitors (ICIs); immunotherapy; lymphoma.
© 2021 British Society for Immunology.
Conflict of interest statement
The authors have no conflicts of interest to declare.
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