Cargando…
A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines
Nucleotide based vaccines represent an enticing, novel approach to vaccination. We have developed a novel immunization technology, RNActive(®) vaccines, that have two important characteristics: mRNA molecules are used whose protein expression capacity has been enhanced by 4 to 5 orders of magnitude...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906413/ https://www.ncbi.nlm.nih.gov/pubmed/23921513 http://dx.doi.org/10.4161/hv.25181 |
_version_ | 1782301479897399296 |
---|---|
author | Kallen, Karl-Josef Heidenreich, Regina Schnee, Margit Petsch, Benjamin Schlake, Thomas Thess, Andreas Baumhof, Patrick Scheel, Birgit Koch, Sven D Fotin-Mleczek, Mariola |
author_facet | Kallen, Karl-Josef Heidenreich, Regina Schnee, Margit Petsch, Benjamin Schlake, Thomas Thess, Andreas Baumhof, Patrick Scheel, Birgit Koch, Sven D Fotin-Mleczek, Mariola |
author_sort | Kallen, Karl-Josef |
collection | PubMed |
description | Nucleotide based vaccines represent an enticing, novel approach to vaccination. We have developed a novel immunization technology, RNActive(®) vaccines, that have two important characteristics: mRNA molecules are used whose protein expression capacity has been enhanced by 4 to 5 orders of magnitude by modifications of the nucleotide sequence with the naturally occurring nucleotides A (adenosine), G (guanosine), C (cytosine), U (uridine) that do not affect the primary amino acid sequence. Second, they are complexed with protamine and thus activate the immune system by involvement of toll-like receptor (TLR) 7. Essentially, this bestows self-adjuvant activity on RNActive(®) vaccines. RNActive(®) vaccines induce strong, balanced immune responses comprising humoral and cellular responses, effector and memory responses as well as activation of important subpopulations of immune cells, such as Th1 and Th2 cells. Pre-germinal center and germinal center B cells were detected in human patients upon vaccination. RNActive(®) vaccines successfully protect against lethal challenges with a variety of different influenza strains in preclinical models. Anti-tumor activity was observed preclinically under therapeutic as well as prophylactic conditions. Initial clinical experiences suggest that the preclinical immunogenicity of RNActive(®) could be successfully translated to humans. |
format | Online Article Text |
id | pubmed-3906413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-39064132014-02-07 A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines Kallen, Karl-Josef Heidenreich, Regina Schnee, Margit Petsch, Benjamin Schlake, Thomas Thess, Andreas Baumhof, Patrick Scheel, Birgit Koch, Sven D Fotin-Mleczek, Mariola Hum Vaccin Immunother Review Nucleotide based vaccines represent an enticing, novel approach to vaccination. We have developed a novel immunization technology, RNActive(®) vaccines, that have two important characteristics: mRNA molecules are used whose protein expression capacity has been enhanced by 4 to 5 orders of magnitude by modifications of the nucleotide sequence with the naturally occurring nucleotides A (adenosine), G (guanosine), C (cytosine), U (uridine) that do not affect the primary amino acid sequence. Second, they are complexed with protamine and thus activate the immune system by involvement of toll-like receptor (TLR) 7. Essentially, this bestows self-adjuvant activity on RNActive(®) vaccines. RNActive(®) vaccines induce strong, balanced immune responses comprising humoral and cellular responses, effector and memory responses as well as activation of important subpopulations of immune cells, such as Th1 and Th2 cells. Pre-germinal center and germinal center B cells were detected in human patients upon vaccination. RNActive(®) vaccines successfully protect against lethal challenges with a variety of different influenza strains in preclinical models. Anti-tumor activity was observed preclinically under therapeutic as well as prophylactic conditions. Initial clinical experiences suggest that the preclinical immunogenicity of RNActive(®) could be successfully translated to humans. Landes Bioscience 2013-10-01 2013-06-04 /pmc/articles/PMC3906413/ /pubmed/23921513 http://dx.doi.org/10.4161/hv.25181 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Review Kallen, Karl-Josef Heidenreich, Regina Schnee, Margit Petsch, Benjamin Schlake, Thomas Thess, Andreas Baumhof, Patrick Scheel, Birgit Koch, Sven D Fotin-Mleczek, Mariola A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines |
title | A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines |
title_full | A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines |
title_fullStr | A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines |
title_full_unstemmed | A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines |
title_short | A novel, disruptive vaccination technology: Self-adjuvanted RNActive(®) vaccines |
title_sort | novel, disruptive vaccination technology: self-adjuvanted rnactive(®) vaccines |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906413/ https://www.ncbi.nlm.nih.gov/pubmed/23921513 http://dx.doi.org/10.4161/hv.25181 |
work_keys_str_mv | AT kallenkarljosef anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT heidenreichregina anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT schneemargit anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT petschbenjamin anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT schlakethomas anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT thessandreas anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT baumhofpatrick anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT scheelbirgit anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT kochsvend anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT fotinmleczekmariola anoveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT kallenkarljosef noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT heidenreichregina noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT schneemargit noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT petschbenjamin noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT schlakethomas noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT thessandreas noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT baumhofpatrick noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT scheelbirgit noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT kochsvend noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines AT fotinmleczekmariola noveldisruptivevaccinationtechnologyselfadjuvantedrnactivevaccines |