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      Molecular biology of canine parainfluenza virus V protein and its potential applications in tumor immunotherapy

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          Abstract

          Canine parainfluenza virus (CPIV) is a zoonotic virus that is widely distributed and is the main pathogen causing canine infectious respiratory disease (CIRD), also known as “kennel cough,” in dogs. The CPIV-V protein is the only nonstructural protein of the virus and plays an important role in multiple stages of the virus life cycle by inhibiting apoptosis, altering the host cell cycle and interfering with the interferon response. In addition, studies have shown that the V protein has potential applications in the field of immunotherapy in oncolytic virus therapy or self-amplifying RNA vaccines. In this review, the biosynthesis, structural characteristics and functions of the CPIV-V protein are reviewed with an emphasis on how it facilitates viral immune escape and its potential applications in the field of immunotherapy. Therefore, this review provides a scientific basis for research into the CPIV-V protein and its potential applications.

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          Most cited references105

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          Suppression of RNA recognition by Toll-like receptors: the impact of nucleoside modification and the evolutionary origin of RNA.

          DNA and RNA stimulate the mammalian innate immune system through activation of Toll-like receptors (TLRs). DNA containing methylated CpG motifs, however, is not stimulatory. Selected nucleosides in naturally occurring RNA are also methylated or otherwise modified, but the immunomodulatory effects of these alterations remain untested. We show that RNA signals through human TLR3, TLR7, and TLR8, but incorporation of modified nucleosides m5C, m6A, m5U, s2U, or pseudouridine ablates activity. Dendritic cells (DCs) exposed to such modified RNA express significantly less cytokines and activation markers than those treated with unmodified RNA. DCs and TLR-expressing cells are potently activated by bacterial and mitochondrial RNA, but not by mammalian total RNA, which is abundant in modified nucleosides. We conclude that nucleoside modifications suppress the potential of RNA to activate DCs. The innate immune system may therefore detect RNA lacking nucleoside modification as a means of selectively responding to bacteria or necrotic tissue.
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            Is It Time to Start Transitioning From 2D to 3D Cell Culture?

            Cell culture is an important and necessary process in drug discovery, cancer research, as well as stem cell study. Most cells are currently cultured using two-dimensional (2D) methods but new and improved methods that implement three-dimensional (3D) cell culturing techniques suggest compelling evidence that much more advanced experiments can be performed yielding valuable insights. When performing 3D cell culture experiments, the cell environment can be manipulated to mimic that of a cell in vivo and provide more accurate data about cell-to-cell interactions, tumor characteristics, drug discovery, metabolic profiling, stem cell research, and other types of diseases. Scaffold based techniques such as hydrogel-based support, polymeric hard material-based support, hydrophilic glass fiber, and organoids are employed, and each provide their own advantages and applications. Likewise, there are also scaffold free techniques used such as hanging drop microplates, magnetic levitation, and spheroid microplates with ultra-low attachment coating. 3D cell culture has the potential to provide alternative ways to study organ behavior via the use of organoids and is expected to eventually bridge the gap between 2D cell culture and animal models. The present review compares 2D cell culture to 3D cell culture, provides the details surrounding the different 3D culture techniques, as well as focuses on the present and future applications of 3D cell culture.
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              COVID-19 vaccines: modes of immune activation and future challenges

              The new vaccines against SARS-CoV-2 are novel in terms of specificity, their wide dissemination across the global population and the inclusion of newly licensed mRNA platforms. We discuss here how the approved vaccines trigger innate immunity to promote durable immunological memory and consider the future implications of protecting populations with these vaccines.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2418241/overviewRole: Role: Role:
                Role: Role: Role:
                Role: Role: Role: Role:
                Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1610795/overviewRole: Role: Role:
                URI : https://loop.frontiersin.org/people/1968388/overviewRole: Role: Role: Role:
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                20 December 2023
                2023
                : 14
                : 1282112
                Affiliations
                [1] 1Wenzhou Key Laboratory for Virology and Immunology, Institute of Virology, Wenzhou University , Wenzhou, China
                [2] 2College of Food and Drugs, Luoyang Polytechnic , Luoyang, China
                [3] 3Animal Diseases and Public Health Engineering Research Center of Henan Province , Luoyang, China
                [4] 4Preventive Veterinary Laboratory, College of Animal Science and Technology, Inner Mongolia Minzu University , Tongliao, China
                Author notes

                Edited by: Wei Wei, First Affiliated Hospital of Jilin University, China

                Reviewed by: Mohsan Ullah Goraya, Huaqiao University, China; Verónica Martín García, Immunology and Infectious Diseases Control Director (CISA-INIA-CSIC), Spain

                *Correspondence: Jingqiang Ren, rjq207@ 123456163.com

                These authors have contributed equally to this work

                Article
                10.3389/fmicb.2023.1282112
                10761501
                38173672
                a0f4c9f5-9d6a-466a-b0f1-bfd4ec929025
                Copyright © 2023 Cheng, Zhang, Cai, Liu, Wen and Ren.

                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
                : 23 August 2023
                : 29 November 2023
                Page count
                Figures: 4, Tables: 3, Equations: 0, References: 105, Pages: 15, Words: 10958
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by the Youth Growth Technology Project of Jilin Provincial Science and Technology Development Program (no. 20210508019RQ) and the Start-Up Research Fund from Wenzhou University (no. QD2023014).
                Categories
                Microbiology
                Review
                Custom metadata
                Virology

                Microbiology & Virology
                canine parainfluenza virus,v protein,molecular mechanism,structure,viral replication,immune escape,tumor immunotherapy

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