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

Author:

Adhikary Subhamay1ORCID,Pathak Surajit1ORCID,Palani Vignesh2,Acar Ahmet3ORCID,Banerjee Antara1ORCID,Al-Dewik Nader I.4ORCID,Essa Musthafa Mohamed5ORCID,Mohammed Sawsan G. A. A.6ORCID,Qoronfleh M. Walid7ORCID

Affiliation:

1. Medical Biotechnology, Faculty of Allied Health Sciences, Chettinad Academy of Research and Education (CARE), Chettinad Hospital and Research Institute (CHRI), Chennai 603103, India

2. Faculty of Medicine, Chettinad Hospital and Research Institute (CHRI), Chennai 603103, India

3. Department of Biological Sciences, Middle East Technical University, 06800 Ankara, Türkiye

4. Department of Pediatrics, Women’s Wellness and Research Center, Hamad Medical Corporation, Doha 00974, Qatar

5. College of Agricultural and Marine Sciences, Sultan Qaboos University, Muscat 123, Oman

6. QU Health, College of Medicine, Qatar University, Doha 00974, Qatar

7. Research & Policy Division, Q3 Research Institute (QRI), Ypsilanti, MI 48917, USA

Abstract

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-1β, IL-2, IL-6, and IL-10, and IFN-γ and TNF-α, 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.

Publisher

MDPI AG

Reference216 articles.

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