Affiliation:
1. Department of Pharmacy, Luzhou People's Hospital, Luzhou 646000, Sichuan, PRC China
2. Department of Pharmacy, Luzhou People's Hospital, Luzhou 646000, Sichuan PRC China
3. Shenzhen University Medical
School, Shenzhen University, Shenzhen 518060, China
Abstract
Abstract:
Chimeric antigen receptor T-cells, known as CAR-T cells, represent a promising
breakthrough in the realm of adoptive cell therapy. These T-cells are genetically engineered to
carry chimeric antigen receptors that specifically target tumors. They have achieved notable
success in the treatment of blood-related cancers, breathing new life into this field of medical
research. However, numerous obstacles limit chimeric antigen receptors T-cell therapy's efficacy,
such as it cannot survive in the body long. It is prone to fatigue and exhaustion, leading to
difficult tumor elimination and repeated recurrence, affecting solid tumors and hematological
malignancies. The challenges posed by solid tumors, especially in the context of the complex
solid-tumor microenvironment, require specific strategies. This review outlines recent advancements
in improving chimeric antigen receptors T-cell therapy by focusing on the chimeric
antigen receptors protein, modifying T-cells, and optimizing the interaction between T-cells and
other components within the tumor microenvironment. This article aims to provide an extensive
summary of the latest discoveries regarding CAR-T cell therapy, encompassing its application
across various types of human cancers. Moreover, it will delve into the obstacles that have
emerged in recent times, offering insights into the challenges faced by this innovative approach.
Finally, it highlights novel therapeutic options in treating hematological and solid malignancies
with chimeric antigen receptors T-cell therapies.
Publisher
Bentham Science Publishers Ltd.