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Review
. 2023 Jan-Dec:22:15330338231204198.
doi: 10.1177/15330338231204198.

Current Situation and Prospect of Adoptive Cellular Immunotherapy for Malignancies

Affiliations
Review

Current Situation and Prospect of Adoptive Cellular Immunotherapy for Malignancies

Dong Zhao et al. Technol Cancer Res Treat. 2023 Jan-Dec.

Abstract

Adoptive cell immunotherapy (ACT) is an innovative promising treatment for tumors. ACT is characterized by the infusion of active anti-tumor immune cells (specific and non-specific) into patients to kill tumor cells either directly or indirectly by stimulating the body's immune system. The patient's (autologous) or a donor's (allogeneic) immune cells are used to improve immune function. Chimeric antigen receptor (CAR) T cells (CAR-T) is a type of ACT that has gained attention. T cells from the peripheral blood are genetically engineered to express CARs that rapidly proliferate and specifically recognize target antigens to exert its anti-tumor effects. Clinical application of CAR-T therapy for hematological tumors has shown good results, but adverse reactions and recurrence limit its applicability. Tumor infiltrating lymphocyte (TIL) therapy is effective for solid tumors. TIL therapy exhibits T cell receptor (TCR) clonality, superior tumor homing ability, and low targeted toxicity, but its successful application is limited to a number of tumors. Regardless, TIL and CAR-T therapies are effective for treating cancer. Additionally, CAR-natural killer (NK), CAR-macrophages (M), and TCR-T therapies are currently being researched. In this review, we highlight the current developments and limitations of several types of ACT.

Keywords: CAR-NK; CAR-T; CAR-macrophage; TCR-T; TIL; immunotherapy.

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Conflict of interest statement

Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
TIL therapy process.
Figure 2.
Figure 2.
Different generations of CAR-T cells.
Figure 3.
Figure 3.
Historic timeline of the development of CAR-T cells.
Figure 4.
Figure 4.
Evolution of ACTs for malignancies.

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