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      Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection

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          Abstract

          Measles is the most contagious airborne viral infection and the leading cause of child death among vaccine-preventable diseases. We show here that aerosolized lipopeptide fusion inhibitors, derived from heptad-repeat regions of the measles virus (MeV) fusion protein, block respiratory MeV infection in a non-human primate model, the cynomolgus macaque. We used a custom-designed mesh nebulizer to ensure efficient aerosol delivery of peptides to the respiratory tract and demonstrated the absence of adverse effects and lung pathology in macaques. The nebulized peptide efficiently prevented MeV infection, resulting in the complete absence of MeV RNA, MeV-infected cells, and MeV-specific humoral responses in treated animals. This strategy provides an additional shield which complements vaccination to fight against respiratory infection, presenting a proof-of-concept for the aerosol delivery of fusion inhibitory peptides to protect against measles and other airborne viruses, including SARS-CoV-2, in case of high-risk exposure, that can be readily translated to human trials.

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          Most cited references69

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          Viral membrane fusion.

          Membrane fusion is an essential step when enveloped viruses enter cells. Lipid bilayer fusion requires catalysis to overcome a high kinetic barrier; viral fusion proteins are the agents that fulfill this catalytic function. Despite a variety of molecular architectures, these proteins facilitate fusion by essentially the same generic mechanism. Stimulated by a signal associated with arrival at the cell to be infected (e.g., receptor or co-receptor binding, proton binding in an endosome), they undergo a series of conformational changes. A hydrophobic segment (a "fusion loop" or "fusion peptide") engages the target-cell membrane and collapse of the bridging intermediate thus formed draws the two membranes (virus and cell) together. We know of three structural classes for viral fusion proteins. Structures for both pre- and postfusion conformations of illustrate the beginning and end points of a process that can be probed by single-virion measurements of fusion kinetics.
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            Rescue of measles viruses from cloned DNA.

            A system has been established allowing the rescue of replicating measles viruses (MVs) from cloned DNA. On one hand, plasmids were constructed from which MV antigenomic RNAs with the correct termini are transcribed by phage T7 RNA polymerase. On the other hand, helper cells derived from the human embryonic kidney 293 cell line were generated constitutively expressing T7 RNA polymerase together with MV nucleocapsid protein and phosphoprotein. Simultaneous transfection of the helper cells with the MV antigenomic plasmid and with a plasmid encoding the MV polymerase under direction of a T7 promoter led to formation of syncytia from which MVs were easily recovered. A genetic tag comprising three nucleotide changes was present in the progeny virus. As a first application of reverse genetics, a segment of 504 nucleotides from the 5' non-coding region of the fusion gene was deleted, leading to an MV variant whose replication behaviour in Vero cells was indistinguishable from that of the laboratory Edmonston B strain. Since no helper virus is involved, this system, in principle, should be applicable to the rescue of any member of the large virus order Mononegavirales, i.e. viruses with a nonsegmented negative-strand RNA genome.
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              Needle-free vaccine delivery.

              The search for methods of vaccine delivery not requiring a needle and syringe has been accelerated by recent concerns regarding pandemic disease, bioterrorism, and disease eradication campaigns. Needle-free vaccine delivery could aid in these mass vaccinations by increasing ease and speed of delivery, and by offering improved safety and compliance, decreasing costs, and reducing pain associated with vaccinations. In this article, we summarize the rationale for delivery of needle-free vaccines and discuss several methods currently in use and under development, focusing on needle-free injection devices, transcutaneous immunization, and mucosal immunization. Jet injectors are needle-free devices that deliver liquid vaccine through a nozzle orifice and penetrate the skin with a high-speed narrow stream. They generate improved or equivalent immune responses compared with needle and syringe. Powder injection, a form of jet injection using vaccines in powder form, may obviate the need for the "cold chain." Transcutaneous immunization involves applying vaccine antigen and adjuvant to the skin, using a patch or "microneedles," and can induce both systemic and mucosal immunity. Mucosal immunization has thus far been focused on oral, nasal, and aerosol vaccines. Promising newer technologies in oral vaccination include using attenuated bacteria as vectors and transgenic plant "edible" vaccines. Improved knowledge regarding the immune system and its responses to vaccination continues to inform vaccine technologies for needle-free vaccine delivery.
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                Author and article information

                Journal
                Res Sq
                ResearchSquare
                Research Square
                American Journal Experts
                01 June 2022
                : rs.3.rs-1700877
                Affiliations
                [1 ]CIRI, Centre International de Recherche en Infectiologie, INSERM U1111, CNRS, UMR5308, Univ Lyon, Université Claude Bernard Lyon 1, École Normale Supérieure de Lyon, 21 Avenue Tony Garnier, 69007 Lyon, France.
                [2 ]DTF-Aerodrug, R&D aerosolltherapy department of DTF medical (Saint Etienne, France), Faculté de médecine, Université de Tours, 37032 Tours, France.
                [3 ]Université de Tours, Institut national de recherche pour l’agriculture, l’alimentation et l’environnement (INRAe), UMR1282, Infectiologie et santé publique (ISP), Tours, France.
                [4 ]PST-A, Université de Tours, Tours, France.
                [5 ]INSERM, Research Center for Respiratory Diseases, CEPR U1100, Université de Tours, 37032 Tours, France.
                [6 ]Center for Host-Pathogen Interaction, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
                [7 ]Laboratory of Infection and Virology, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health, Beijing 100045, China
                [8 ]Department of Laboratory Medicine and Pathology, University of Washington Medical Center, Seattle, WA, USA
                [9 ]Robert Frederick Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York, USA
                [10 ]Department of Microbiology and Immunology, Columbia University Vagelos College of Physicians & Surgeons, New York, NY, USA.
                [11 ]Department of Physiology & Cellular Biophysics, Columbia University Vagelos College of Physicians & Surgeons, New York, NY, USA.
                [12 ]Department of Experimental Medicine, University of Studies of Campania ‘Luigi Vanvitelli’, Naples, Italy.
                Author notes

                Author contributions: Conceptualization: BH, OR, LV, MI, AM, MP, CM; Methodology: OR, CD, CG, MI, SLG, LV, JM, CM, ALG, CAA; Investigation: OR, LV, JM, MI, CD, CG, SLG, CM, LL, MF, YZ, DLP, GC, GR, AA; Funding acquisition: BH, MP; Project administration: BH, MP; Supervision: BH, OR, CD, MI, CM; Writing – original draft: OR, MI, BH; Writing – review & editing: OR, BH, MI, MP, AM.

                Address correspondence to: Branka Horvat, CIRI, 21 Avenue Tony Garnier, 69007 Lyon, France, tel: +33 4 3728 2392, branka.horvat@ 123456inserm.fr
                Author information
                http://orcid.org/0000-0001-7536-355X
                http://orcid.org/0000-0001-7511-1512
                http://orcid.org/0000-0002-8946-3049
                http://orcid.org/0000-0001-7299-6407
                http://orcid.org/0000-0002-6682-2029
                http://orcid.org/0000-0003-2654-018X
                http://orcid.org/0000-0002-1796-8320
                http://orcid.org/0000-0003-3866-9220
                http://orcid.org/0000-0003-0578-7765
                Article
                10.21203/rs.3.rs-1700877
                10.21203/rs.3.rs-1700877/v1
                9176655
                35677066
                070327ea-6d82-4ce0-b8dc-241942e2284b

                This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.

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