T Cell Based Immunotherapy for Cancer: Approaches and Strategies

被引:28
作者
Want, Muzamil Y. [1 ]
Bashir, Zeenat [2 ]
Najar, Rauf A. [3 ]
机构
[1] Roswell Park Comprehens Canc Ctr, Dept Immunol, Div Translat Immuno Oncol, Buffalo, NY 14263 USA
[2] Canisius Coll, Dept Chem & Biochem, Buffalo, NY 14208 USA
[3] Univ Rochester, Dept Pediat, Lung Biol & Dis Program, Sch Med & Dent, Rochester, NY 14642 USA
关键词
T cells; immunotherapy; neoantigens; cancer antigens; TCR engineering; HLA restriction; chimeric antigen receptor; CAR NK cells; CAR MIAT; CHIMERIC ANTIGEN RECEPTOR; RECENT THYMIC EMIGRANTS; METASTATIC MELANOMA; ANTITUMOR-ACTIVITY; GENE-THERAPY; MAIT CELLS; TUMOR; LYMPHOCYTES; IDENTIFICATION; GAMMA;
D O I
10.3390/vaccines11040835
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cells are critical in destroying cancer cells by recognizing antigens presented by MHC molecules on cancer cells or antigen-presenting cells. Identifying and targeting cancer-specific or overexpressed self-antigens is essential for redirecting T cells against tumors, leading to tumor regression. This is achieved through the identification of mutated or overexpressed self-proteins in cancer cells, which guide the recognition of cancer cells by T-cell receptors. There are two main approaches to T cell-based immunotherapy: HLA-restricted and HLA-non-restricted Immunotherapy. Significant progress has been made in T cell-based immunotherapy over the past decade, using naturally occurring or genetically engineered T cells to target cancer antigens in hematological malignancies and solid tumors. However, limited specificity, longevity, and toxicity have limited success rates. This review provides an overview of T cells as a therapeutic tool for cancer, highlighting the advantages and future strategies for developing effective T cell cancer immunotherapy. The challenges associated with identifying T cells and their corresponding antigens, such as their low frequency, are also discussed. The review further examines the current state of T cell-based immunotherapy and potential future strategies, such as the use of combination therapy and the optimization of T cell properties, to overcome current limitations and improve clinical outcomes.
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页数:19
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