Articles citing this article

The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).

Cited article:

Thomas Démoulins, Navapon Techakriengkrai, Thomas Ebensen, Kai Schulze, Matthias Liniger, Markus Gerber, Teerawut Nedumpun, Kenneth C. McCullough, Carlos A. Guzmán, Sanipa Suradhat and Nicolas Ruggli
2786 89 (2024)
https://doi.org/10.1007/978-1-0716-3770-8_4

Construction and efficacy of a new live chimeric C-strain vaccine with DIVA characteristics against classical swine fever

Weicheng Yi, Hao Wang, Huan Qin, Qin Wang, Rui Guo, Guoyuan Wen and Zishu Pan
Vaccine 41 (12) 2003 (2023)
https://doi.org/10.1016/j.vaccine.2023.02.044

Coatsome-replicon vehicles: Self-replicating RNA vaccines against infectious diseases

Thomas Démoulins, Kai Schulze, Thomas Ebensen, Navapon Techakriengkrai, Teerawut Nedumpun, Pavlos C. Englezou, Markus Gerber, Ruslan Hlushchuk, Darien Toledo, Valentin Djonov, Stephan von Gunten, Kenneth C. McCullough, Matthias Liniger, Carlos A. Guzmán, Sanipa Suradhat and Nicolas Ruggli
Nanomedicine: Nanotechnology, Biology and Medicine 49 102655 (2023)
https://doi.org/10.1016/j.nano.2023.102655

Skin-Based Vaccination: A Systematic Mapping Review of the Types of Vaccines and Methods Used and Immunity and Protection Elicited in Pigs

Inés Có-Rives, Ann Ying-An Chen and Anne C. Moore
Vaccines 11 (2) 450 (2023)
https://doi.org/10.3390/vaccines11020450

Reduced Virus Load in Lungs of Pigs Challenged with Porcine Reproductive and Respiratory Syndrome Virus after Vaccination with Virus Replicon Particles Encoding Conserved PRRSV Cytotoxic T-Cell Epitopes

Simon Welner, Nicolas Ruggli, Matthias Liniger, Artur Summerfield, Lars Erik Larsen and Gregers Jungersen
Vaccines 9 (3) 208 (2021)
https://doi.org/10.3390/vaccines9030208

Self-Amplifying Pestivirus Replicon RNA Encoding Influenza Virus Nucleoprotein and Hemagglutinin Promote Humoral and Cellular Immune Responses in Pigs

Thomas Démoulins, Nicolas Ruggli, Markus Gerber, et al.
Frontiers in Immunology 11 (2021)
https://doi.org/10.3389/fimmu.2020.622385

A Critical Review about Different Vaccines against Classical Swine Fever Virus and Their Repercussions in Endemic Regions

Liani Coronado, Carmen L. Perera, Liliam Rios, María T. Frías and Lester J. Pérez
Vaccines 9 (2) 154 (2021)
https://doi.org/10.3390/vaccines9020154

Autonomously Replicating RNAs of Bungowannah Pestivirus: E RNS Is Not Essential for the Generation of Infectious Particles

Anja Dalmann, Ilona Reimann, Kerstin Wernike, Martin Beer and Mark T. Heise
Journal of Virology 94 (14) (2020)
https://doi.org/10.1128/JVI.00436-20

Roles of secretory glycoproteins in particle formation of Flaviviridae viruses

Takasuke Fukuhara and Yoshiharu Matsuura
Microbiology and Immunology 63 (10) 401 (2019)
https://doi.org/10.1111/1348-0421.12733

Self-replicating RNA vaccine functionality modulated by fine-tuning of polyplex delivery vehicle structure

Thomas Démoulins, Thomas Ebensen, Kai Schulze, Pavlos C. Englezou, Maria Pelliccia, Carlos A. Guzmán, Nicolas Ruggli and Kenneth C. McCullough
Journal of Controlled Release 266 256 (2017)
https://doi.org/10.1016/j.jconrel.2017.09.018

Virus replicon particle vaccines expressing nucleoprotein of influenza A virus mediate enhanced inflammatory responses in pigs

Meret E. Ricklin, Sylvie Python, Nathalie J. Vielle, et al.
Scientific Reports 7 (1) (2017)
https://doi.org/10.1038/s41598-017-16419-w

Polyethylenimine-based polyplex delivery of self-replicating RNA vaccines

Thomas Démoulins, Panagiota Milona, Pavlos C. Englezou, et al.
Nanomedicine: Nanotechnology, Biology and Medicine 12 (3) 711 (2016)
https://doi.org/10.1016/j.nano.2015.11.001

T-cell reprogramming through targeted CD4-coreceptor and T-cell receptor expression on maturing thymocytes by latentCircoviridaefamily member porcine circovirus type 2 cell infections in the thymus

Stefanie Klausmann, Titus Sydler, Summerfield Artur, et al.
Emerging Microbes & Infections 4 (1) 1 (2015)
https://doi.org/10.1038/emi.2015.15

Co-expression of the C-terminal domain of Yersinia enterocolitica invasin enhances the efficacy of classical swine-fever-vectored vaccine based on human adenovirus

Helin Li, Pengbo Ning, Zhi Lin, et al.
Journal of Biosciences 40 (1) 79 (2015)
https://doi.org/10.1007/s12038-014-9495-z

Global Virology I - Identifying and Investigating Viral Diseases

Hana Van Campen, Guillermo Risatti, Manuel Borca, et al.
Global Virology I - Identifying and Investigating Viral Diseases 361 (2015)
https://doi.org/10.1007/978-1-4939-2410-3_14

Self-replicating Replicon-RNA Delivery to Dendritic Cells by Chitosan-nanoparticles for Translation In Vitro and In Vivo

Kenneth C McCullough, Isabelle Bassi, Panagiota Milona, et al.
Molecular Therapy - Nucleic Acids 3 e173 (2014)
https://doi.org/10.1038/mtna.2014.24

Classical swine fever in pigs: recent developments and future perspectives

Vishal Chander, S. Nandi, C. Ravishankar, V. Upmanyu and Rishendra Verma
Animal Health Research Reviews 15 (1) 87 (2014)
https://doi.org/10.1017/S1466252314000024

Analysis of classical swine fever virus RNA replication determinants using replicons

Peter Christian Risager, Ulrik Fahnøe, Maria Gullberg, Thomas Bruun Rasmussen and Graham J. Belsham
Journal of General Virology 94 (8) 1739 (2013)
https://doi.org/10.1099/vir.0.052688-0

Efficient Sensing of Infected Cells in Absence of Virus Particles by Blasmacytoid Dendritic Cells Is Blocked by the Viral Ribonuclease Erns

Sylvie Python, Markus Gerber, Rolf Suter, et al.
PLoS Pathogens 9 (6) e1003412 (2013)
https://doi.org/10.1371/journal.ppat.1003412

Recombinant chimeric vaccine composed of PRRSV antigens and truncated Pseudomonas exotoxin A (PE-K13)

Hsin-Ping Yang, Tsan-Chih Wang, Shiou-Jen Wang, et al.
Research in Veterinary Science 95 (2) 742 (2013)
https://doi.org/10.1016/j.rvsc.2013.05.003

Chimeric classical swine fever (CSF)-Japanese encephalitis (JE) viral replicon as a non-transmissible vaccine candidate against CSF and JE infections

Zhenhua Yang, Rui Wu, Robert W. Li, et al.
Virus Research 165 (1) 61 (2012)
https://doi.org/10.1016/j.virusres.2012.01.007

Comparative evaluation of live marker vaccine candidates “CP7_E2alf” and “flc11” along with C-strain “Riems” after oral vaccination

Sandra Blome, Andrea Aebischer, Elke Lange, et al.
Veterinary Microbiology 158 (1-2) 42 (2012)
https://doi.org/10.1016/j.vetmic.2012.02.015

Functional RNA Delivery Targeted to Dendritic Cells By Synthetic Nanoparticles

Kenneth C McCullough, Isabelle Bassi, Thomas Démoulins, Lisa J Thomann-Harwood and Nicolas Ruggli
Therapeutic Delivery 3 (9) 1077 (2012)
https://doi.org/10.4155/tde.12.90

Immunogenic and replicative properties of classical swine fever virus replicon particles modified to induce IFN-α/β and carry foreign genes

Rolf Suter, Artur Summerfield, Lisa J. Thomann-Harwood, et al.
Vaccine 29 (7) 1491 (2011)
https://doi.org/10.1016/j.vaccine.2010.12.026

New insights into processing of bovine viral diarrhea virus glycoproteins Erns and E1

Anne Wegelt, Ilona Reimann, Johanna Zemke and Martin Beer
Journal of General Virology 90 (10) 2462 (2009)
https://doi.org/10.1099/vir.0.012559-0

Chimeric pestiviruses: candidates for live-attenuated classical swine fever marker vaccines

Franziska Wehrle, Sandra Renzullo, Anja Faust, et al.
Journal of General Virology 88 (8) 2247 (2007)
https://doi.org/10.1099/vir.0.82798-0

Efficient priming against classical swine fever with a safe glycoprotein E2 expressing Orf virus recombinant (ORFV VrV-E2)

Heiner Voigt, Catherine Merant, Daniel Wienhold, et al.
Vaccine 25 (31) 5915 (2007)
https://doi.org/10.1016/j.vaccine.2007.05.035

Packaged replicons of bovine viral diarrhea virus are capable of inducing a protective immune response

Ilona Reimann, Ilia Semmler and Martin Beer
Virology 366 (2) 377 (2007)
https://doi.org/10.1016/j.virol.2007.05.006