Abstract

RNA viruses have been subjected to substantial engineering efforts to support gene therapy applications and vaccine development. Typically, retroviruses, lentiviruses, alphaviruses, flaviviruses rhabdoviruses, measles viruses, Newcastle disease viruses, and picornaviruses have been employed as expression vectors for treatment of various diseases including different types of cancers, hemophilia, and infectious diseases. Moreover, vaccination with viral vectors has evaluated immunogenicity against infectious agents and protection against challenges with pathogenic organisms. Several preclinical studies in animal models have confirmed both immune responses and protection against lethal challenges. Similarly, administration of RNA viral vectors in animals implanted with tumor xenografts resulted in tumor regression and prolonged survival, and in some cases complete tumor clearance. Based on preclinical results, clinical trials have been conducted to establish the safety of RNA virus delivery. Moreover, stem cell-based lentiviral therapy provided life-long production of factor VIII potentially generating a cure for hemophilia A. Several clinical trials on cancer patients have generated anti-tumor activity, prolonged survival, and even progression-free survival.

Highlights

  • The application of viral vectors in gene therapy and vaccine development dates back to the1990s [1]

  • The early days of gene therapy were overshadowed by set-backs related to the death of a young patient treated with adenovirus vectors for a none-life threating disease [2], and the unexpected development of leukemia in retrovirus-based therapy of children with severe combined immunodeficiency (SCID) [3,4], recent development has been encouraging

  • An overview is given on RNA virus-based vectors and their applications for treatment of various cancers and hemophilia, and for immunization studies aiming at providing protection against challenges with infectious agents and cancer-inducing tumor cells

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Summary

Introduction

The application of viral vectors in gene therapy and vaccine development dates back to the. Progress has been achieved for both viral and non-viral vectors providing excellent possibilities for applications in gene therapy and vaccine development, the focus in this review is entirely on virus-based delivery systems. In this context, an overview is given on RNA virus-based vectors and their applications for treatment of various cancers and hemophilia, and for immunization studies aiming at providing protection against challenges with infectious agents and cancer-inducing tumor cells

Viral Vectors
Retroviruses
Lentiviruses
Alphaviruses
Flaviviruses
Rhabdoviruses
Measles Viruses
Newcastle Disease Viruses
Picornaviruses
Clinical Trials
Findings
Conclusions
Full Text
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