40
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Development and application of oncolytic viruses as the nemesis of tumor cells

      review-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Viruses and tumors are two pathologies that negatively impact human health, but what occurs when a virus encounters a tumor? A global consensus among cancer patients suggests that surgical resection, chemotherapy, radiotherapy, and other methods are the primary means to combat cancer. However, with the innovation and development of biomedical technology, tumor biotherapy (immunotherapy, molecular targeted therapy, gene therapy, oncolytic virus therapy, etc.) has emerged as an alternative treatment for malignant tumors. Oncolytic viruses possess numerous anti-tumor properties, such as directly lysing tumor cells, activating anti-tumor immune responses, and improving the tumor microenvironment. Compared to traditional immunotherapy, oncolytic virus therapy offers advantages including high killing efficiency, precise targeting, and minimal side effects. Although oncolytic virus (OV) therapy was introduced as a novel approach to tumor treatment in the 19th century, its efficacy was suboptimal, limiting its widespread application. However, since the U.S. Food and Drug Administration (FDA) approved the first OV therapy drug, T-VEC, in 2015, interest in OV has grown significantly. In recent years, oncolytic virus therapy has shown increasingly promising application prospects and has become a major research focus in the field of cancer treatment. This article reviews the development, classification, and research progress of oncolytic viruses, as well as their mechanisms of action, therapeutic methods, and routes of administration.

          Related collections

          Most cited references297

          • Record: found
          • Abstract: not found
          • Article: not found

          Immune-Related Adverse Events Associated with Immune Checkpoint Blockade

            • Record: found
            • Abstract: found
            • Article: not found

            Talimogene Laherparepvec Improves Durable Response Rate in Patients With Advanced Melanoma.

            Talimogene laherparepvec (T-VEC) is a herpes simplex virus type 1-derived oncolytic immunotherapy designed to selectively replicate within tumors and produce granulocyte macrophage colony-stimulating factor (GM-CSF) to enhance systemic antitumor immune responses. T-VEC was compared with GM-CSF in patients with unresected stage IIIB to IV melanoma in a randomized open-label phase III trial.
              • Record: found
              • Abstract: found
              • Article: not found

              ONCOLYTIC VIROTHERAPY

              Oncolytic virotherapy is an emerging treatment modality which uses replication competent viruses to destroy cancers. Advances in the past two years include preclinical proof of feasibility for a single-shot virotherapy cure, identification of drugs that accelerate intratumoral virus propagation, new strategies to maximize the immunotherapeutic potential of oncolytic virotherapy, and clinical confirmation of a critical viremic thereshold for vascular delivery and intratumoral virus replication. The primary clinical milestone was completion of accrual in a phase III trial of intratumoral herpes simplex virus therapy using talimogene laherparepvec for metastatic melanoma. Challenges for the field are to select ‘winners’ from a burgeoning number of oncolytic platforms and engineered derivatives, to transiently suppress but then unleash the power of the immune system to maximize both virus spread and anticancer immunity, to develop more meaningful preclinical virotherapy models and to manufacture viruses with orders of magnitude higher yields compared to established vaccine manufacturing processes.

                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                12 June 2023
                2023
                : 14
                : 1188526
                Affiliations
                [1] 1Zhejiang Provincial People's Hospital Affiliated to Hangzhou Medical College, Hangzhou Medical College , Hangzhou, China
                [2] 2The Marine Biomedical Research Institute, Guangdong Medical University , Zhanjiang, China
                [3] 3Department of Biological and Chemical Sciences, New York Institute of Technology—Manhattan Campus , New York, NY, United States
                [4] 4Department of Clinical Medicine, Medicine and Technology, School of Zunyi Medical University , Zunyi, China
                [5] 5Guangdong Provincial Key Laboratory of Systems Biology and Synthetic Biology for Urogenital Tumors, Shenzhen Key Laboratory of Genitourinary Tumor, Department of Urology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital (Shenzhen Institute of Translational Medicine), Shenzhen, China
                [6] 6Department of Gastroenterology, Zibo Central Hospital , Zibo, China
                [7] 7Department of Clinical Laboratory, Institute of Translational Medicine, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People’s Hospital , Shenzhen, China
                Author notes

                Edited by: Tejabhiram Yadavalli, University of Illinois Chicago, United States

                Reviewed by: Pankaj Sharma, University of Illinois Chicago, United States; Madavaraju Krishnaraju, Northwestern University, United States

                *Correspondence: Xiuqing Liu, liuxiuqing86@ 123456163.com

                These authors have contributed equally to this work

                Article
                10.3389/fmicb.2023.1188526
                10335770
                37440883
                160aa440-e7e6-48cc-b23c-4bb004b104ec
                Copyright © 2023 Zhu, Fan, Xiong, Chen, Li, Tao and Liu.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 March 2023
                : 18 May 2023
                Page count
                Figures: 5, Tables: 6, Equations: 0, References: 297, Pages: 21, Words: 21147
                Funding
                Funded by: The Wu Jieping Medical Foundation Clinical Research Special Grant
                Award ID: 320.6750.2021-06-29
                Categories
                Microbiology
                Review
                Custom metadata
                Virology

                Microbiology & Virology
                anti-tumor immune response,oncolytic virus,tumor cells,pd-1,adenovirus,herpes simplex virus

                Comments

                Comment on this article

                Related Documents Log