Current Technologies and Future Perspectives in Immunotherapy towards a Clinical Oncology Approach

被引:5
|
作者
Adhikary, Subhamay [1 ]
Pathak, Surajit [1 ]
Palani, Vignesh [2 ]
Acar, Ahmet [3 ]
Banerjee, Antara [1 ]
Al-Dewik, Nader I. [4 ]
Essa, Musthafa Mohamed [5 ]
Mohammed, Sawsan G. A. A. [6 ]
Qoronfleh, M. Walid [7 ]
机构
[1] Chettinad Hosp Res & Inst CHRI, Chettinad Acad Res & Educ CARE, Fac Allied Hlth Sci, Med Biotechnol, Chennai 603103, India
[2] Chettinad Hosp & Res Inst CHRI, Fac Med, Chennai 603103, India
[3] Middle East Tech Univ, Dept Biol Sci, TR-06800 Ankara, Turkiye
[4] Hamad Med Corp, Womens Wellness & Res Ctr, Dept Pediat, Doha 00974, Qatar
[5] Sultan Qaboos Univ, Coll Agr & Marine Sci, Muscat 123, Oman
[6] Qatar Univ, Coll Med, QU Hlth, Doha 00974, Qatar
[7] Q3 Res Inst QRI, Res & Policy Div, Ypsilanti, MI 48917 USA
关键词
cancer; immunogenicity; gene therapy; immunotherapy; immune checkpoint; CAR T cell therapy; dendritic cell-based therapy; NK cell-based therapy; CRISPR-Cas9; GROWTH-FACTOR RECEPTOR; PD-1; BLOCKADE; CANCER-IMMUNOTHERAPY; MONOCLONAL-ANTIBODY; ACQUIRED-RESISTANCE; IMMUNE CHECKPOINTS; CYTOKINE STORM; BREAST-CANCER; CLASS-I; CELLS;
D O I
10.3390/biomedicines12010217
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immunotherapy is now established as a potent therapeutic paradigm engendering antitumor immune response against a wide range of malignancies and other diseases by modulating the immune system either through the stimulation or suppression of immune components such as CD4+ T cells, CD8+ T cells, B cells, monocytes, macrophages, dendritic cells, and natural killer cells. By targeting several immune checkpoint inhibitors or blockers (e.g., PD-1, PD-L1, PD-L2, CTLA-4, LAG3, and TIM-3) expressed on the surface of immune cells, several monoclonal antibodies and polyclonal antibodies have been developed and already translated clinically. In addition, natural killer cell-based, dendritic cell-based, and CAR T cell therapies have been also shown to be promising and effective immunotherapeutic approaches. In particular, CAR T cell therapy has benefited from advancements in CRISPR-Cas9 genome editing technology, allowing the generation of several modified CAR T cells with enhanced antitumor immunity. However, the emerging SARS-CoV-2 infection could hijack a patient's immune system by releasing pro-inflammatory interleukins and cytokines such as IL-1 beta, IL-2, IL-6, and IL-10, and IFN-gamma and TNF-alpha, respectively, which can further promote neutrophil extravasation and the vasodilation of blood vessels. Despite the significant development of advanced immunotherapeutic technologies, after a certain period of treatment, cancer relapses due to the development of resistance to immunotherapy. Resistance may be primary (where tumor cells do not respond to the treatment), or secondary or acquired immune resistance (where tumor cells develop resistance gradually to ICIs therapy). In this context, this review aims to address the existing immunotherapeutic technologies against cancer and the resistance mechanisms against immunotherapeutic drugs, and explain the impact of COVID-19 on cancer treatment. In addition, we will discuss what will be the future implementation of these strategies against cancer drug resistance. Finally, we will emphasize the practical steps to lay the groundwork for enlightened policy for intervention and resource allocation to care for cancer patients.
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页数:28
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