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Immune checkpoint inhibitors and cellular treatment for lymphoma immunotherapy
Author(s) -
Li F.,
Chen Y.,
Pang M.,
Yang P.,
Jing H.
Publication year - 2021
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.13592
Subject(s) - immunotherapy , immune system , tigit , immunology , cytotoxic t cell , lymphoma , antigen , chimeric antigen receptor , ctla 4 , t cell , cancer research , biology , medicine , biochemistry , in vitro
Summary 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.

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