Literature DB >> 33543466

Viral Nanoparticles: Cancer Vaccines and Immune Modulators.

Manlio Fusciello1, Erkko Ylösmäki1, Vincenzo Cerullo2,3.   

Abstract

In the last decades, viruses have gained great interest in the field of immuno-oncology (I-O) for their ability of interacting both with the immune system and the tumour microenvironment. Those pathogens have naturally evolved and been evolutionary to specifically infect hosts, replicate, deliver their genome, and spread. These properties, initially considered a disadvantage, have been investigated and edited to turn viruses into precious allies for molecular biology serving as gene therapy vectors, adjuvants for the immune system, drug cargos, and, lately, anticancer therapeutics. As anticancer drug, one interesting option is viral engineering. Modification of either the viral genome or the outer shell of viruses can change infectivity and tissue targeting and add new functions to the viral particle. Remarkably, in the field of cancer virotherapy, scientists realized that a specific viral genomic depletion would turn the normal tropism of viruses to conditionally replicate in cancer cells only. This category of viruses, named 'Oncolytic viruses', have been investigated and used for cancer treatment in the past decades resulting in the approval of the first oncolytic virus, a herpes simplex virus expressing a stimulating factor, named T-Vec, in 2015. As such, oncolytic viruses achieved positive outcome but still are not able to completely eradicate the disease. This has brought the scientific community to edit those agents, adding to their ability to directly lysate cancer cells, few modifications to mainly boost their interaction with the immune system. Viruses experienced then a renaissance not only as infecting agent but as nanoparticle and cancer vaccines too. These strategies bring new life to the concept of using viruses as viral particles for therapeutic applications.

Entities:  

Keywords:  Adenovirus; Cancer vaccines; Capsid surface modification; ExtraCRAd; Gene therapy; Oncolytic viruses; PeptiCrad; PeptiENV; Peptide-loaded capsid; Viral vectors; siRNA; viRNA

Year:  2021        PMID: 33543466     DOI: 10.1007/978-3-030-58174-9_14

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  42 in total

1.  Viral nanoparticles as macromolecular devices for new therapeutic and pharmaceutical approaches.

Authors:  Simone Grasso; Luca Santi
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2010-07-06

Review 2.  Polymer-coated viral vectors: hybrid nanosystems for gene therapy.

Authors:  Pratheppa Rajagopal; Sowmiya Duraiswamy; Swaminathan Sethuraman; Jayandharan Giridhara Rao; Uma Maheswari Krishnan
Journal:  J Gene Med       Date:  2018-03-25       Impact factor: 4.565

3.  A top-down approach for construction of hybrid polymer-virus gene delivery vectors.

Authors:  Joshua D Ramsey; Halong N Vu; Daniel W Pack
Journal:  J Control Release       Date:  2010-01-31       Impact factor: 9.776

Review 4.  Gene therapy using adeno-associated virus vectors.

Authors:  Shyam Daya; Kenneth I Berns
Journal:  Clin Microbiol Rev       Date:  2008-10       Impact factor: 26.132

Review 5.  Viral nanoparticles as platforms for next-generation therapeutics and imaging devices.

Authors:  Nicole F Steinmetz
Journal:  Nanomedicine       Date:  2010-04-28       Impact factor: 5.307

6.  Brief Communication; A Heterologous Oncolytic Bacteria-Virus Prime-Boost Approach for Anticancer Vaccination in Mice.

Authors:  Amelia S Aitken; Dominic G Roy; Nikolas T Martin; Subash Sad; John C Bell; Marie-Claude Bourgeois-Daigneault
Journal:  J Immunother       Date:  2018-04       Impact factor: 4.456

Review 7.  Viral nanoparticles and virus-like particles: platforms for contemporary vaccine design.

Authors:  Emily M Plummer; Marianne Manchester
Journal:  Wiley Interdiscip Rev Nanomed Nanobiotechnol       Date:  2010-09-24

8.  In vivo engineering of lymphocytes after systemic exosome-associated AAV delivery.

Authors:  James J Moon; Casey A Maguire; Cort B Breuer; Killian S Hanlon; Jeya-Shree Natasan; Adrienn Volak; Amine Meliani; Federico Mingozzi; Benjamin P Kleinstiver
Journal:  Sci Rep       Date:  2020-03-11       Impact factor: 4.379

Review 9.  Engineering adeno-associated virus vectors for gene therapy.

Authors:  Chengwen Li; R Jude Samulski
Journal:  Nat Rev Genet       Date:  2020-02-10       Impact factor: 59.581

10.  Gene therapy for severe combined immunodeficiencies and beyond.

Authors:  Alain Fischer; Salima Hacein-Bey-Abina
Journal:  J Exp Med       Date:  2020-01-06       Impact factor: 14.307

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