Literature DB >> 33181204

Off the beaten path: Novel mRNA-nanoformulations for therapeutic vaccination against HIV.

Sigrid D'haese1, Céline Lacroix2, Felipe Garcia3, Montserrat Plana3, Simona Ruta4, Guido Vanham5, Bernard Verrier2, Joeri L Aerts6.   

Abstract

Over the last few years, immunotherapy for HIV in general and therapeutic vaccination in particular, has received a tremendous boost, both in preclinical research and in clinical applications. This interest is based on the evidence that the immune system plays a crucial role in controlling HIV infection, as shown for long-term non-progressors and elite controllers, and that immune responses can be manipulated towards targeting conserved epitopes. So far, the most successful approach has been vaccination with autologous dendritic cells (DCs) loaded ex vivo with antigens and activation signals. Although this approach offers much promise, it also comes with significant drawbacks such as the requirement of a specialized infrastructure and expertise, as well as major challenges for logistics and storage, making it extremely time consuming and costly. Therefore, methods are being developed to avoid the use of ex vivo generated, autologous DCs. One of these methods is based on mRNA for therapeutic vaccination. mRNA has proven to be a very promising vaccine platform, as the coding information for any desired protein, including antigens and activation signals, can be generated in a very short period of time, showing promise both as an off-the-shelf therapy and as a personalized approach. However, an important drawback of this approach is the short half-life of native mRNA, due to the presence of ambient RNases. In addition, proper immunization requires that the antigens are expressed, processed and presented at the right immunological site (e.g. the lymphoid tissues). An ambivalent aspect of mRNA as a vaccine is its capacity to induce type I interferons, which can have beneficial adjuvant effects, but also deleterious effects on mRNA stability and translation. Thus, proper formulation of the mRNA is crucially important. Many approaches for RNA formulation have already been tested, with mixed success. In this review we discuss the state-of-the-art and future trends for mRNA-nanoparticle formulations for HIV vaccination, both in the prophylactic and in the therapeutic setting.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  HIV; Nanoparticles; Therapeutic vaccination; mRNA vaccination

Year:  2020        PMID: 33181204     DOI: 10.1016/j.jconrel.2020.11.009

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  4 in total

Review 1.  HIV mRNA Vaccines-Progress and Future Paths.

Authors:  Zekun Mu; Barton F Haynes; Derek W Cain
Journal:  Vaccines (Basel)       Date:  2021-02-07

Review 2.  Autoimmune and autoinflammatory conditions after COVID-19 vaccination. New case reports and updated literature review.

Authors:  Yhojan Rodríguez; Manuel Rojas; Santiago Beltrán; Fernando Polo; Laura Camacho-Domínguez; Samuel David Morales; M Eric Gershwin; Juan-Manuel Anaya
Journal:  J Autoimmun       Date:  2022-08-24       Impact factor: 14.511

3.  mRNA vaccines: a transformative technology with applications beyond COVID-19.

Authors:  Isabella Overmars; George Au-Yeung; Terence M Nolan; Andrew C Steer
Journal:  Med J Aust       Date:  2022-07-03       Impact factor: 12.776

4.  Efficient Induction of Antigen-Specific CD8+ T-Cell Responses by Cationic Peptide-Based mRNA Nanoparticles.

Authors:  Sigrid D'haese; Thessa Laeremans; Sabine den Roover; Sabine D Allard; Guido Vanham; Joeri L Aerts
Journal:  Pharmaceutics       Date:  2022-06-30       Impact factor: 6.525

  4 in total

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