Systemic DNA immunization against ovine lentivirus using particle-mediated epidermal delivery and modified vaccinia Ankara encoding the gag and/or env genes

Autor: Tom N. McNeilly, Maurizio Mazzei, Craig Watkins, X. de Andrés, H. Arnarson, H. Crespo, C. Huard, Idoia Glaria, Valgerdur Andrésdóttir, Sigurbjörg Torsteinsdóttir, Lluís Luján, Gordon D. Harkiss, Damián F. de Andrés, Cyril Barbezange, Francesco Tolari, C. Liu, I. de Blas, H. Niesalla, Ml Carrozza, G. Pétursson, Christophe Fraisier, Marta M. Pérez, Marie Suzan-Monti, Beatriz Amorena, Juan José Badiola, E. Biescas, Cristina Solano, Ramsés Reina, Sergio Rosati, Barbara Blacklaws, Michel Pépin, D. J. Shaw, P. Bandecchi
Přispěvatelé: CSIC-Public University of Navarra, University of Cambridge [UK] (CAM), Aix-Marseille Université - Faculté de médecine (AMU MED), Aix Marseille Université (AMU), University of Iceland [Reykjavik], University of Zaragoza - Universidad de Zaragoza [Zaragoza], University of Pisa - Università di Pisa, University of Edinburgh, University of Turin, Laboratoire d'études et de recherches sur les petits ruminants et les abeilles, Agence Française de Sécurité Sanitaire des Aliments (AFSSA), Universidad Pública de Navarra [Espagne] = Public University of Navarra (UPNA), Università degli studi di Torino = University of Turin (UNITO), Laboratoire d'études et de recherches sur les petits ruminants et les abeilles (LERPRA), European Commission, Ministerio de Educación y Ciencia (España), Comisión Interministerial de Ciencia y Tecnología, CICYT (España)
Jazyk: angličtina
Rok vydání: 2009
Předmět:
Male
Modified vaccinia Ankara
MESH: Biolistics
Visna-maedi virus
T-Lymphocytes
viruses
DNA vaccination
Antibodies
Viral

env/*genetics/immunology Genes
Gene gun
MESH: Proviruses
Proviruses
MESH: Vaccinia virus
Vaccines
DNA

MESH: Animals
1UVIROLOGIE HAFSSA AUTRE Animals Antibodies
0303 health sciences
biology
Pneumonia
Progressive Interstitial
of Sheep

MESH: Genes
env

MESH: Pneumonia
Progressive Interstitial
of Sheep

Provirus
Genes
gag

3. Good health
MESH: Visna-maedi virus
Infectious Diseases
[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology
Molecular Medicine
MESH: Virion
MESH: Immunization
Female
Antibody
Viral/blood *Biolistics Epidermis/virology Female Genes
Progressive Interstitial
MESH: Sheep
MESH: Genes
gag

Vaccinia virus
Genes
env

Virus
Viral vector
03 medical and health sciences
MESH: Viral Vaccines
Animals
Immune response
Particle-mediated epidermal bombardment
030304 developmental biology
Sheep
General Veterinary
General Immunology and Microbiology
030306 microbiology
Lentivirus
Public Health
Environmental and Occupational Health

Virion
Viral Vaccines
DNA/administration & dosage/genetics/immunology Vaccinia virus/*genetics/immunology Viral Vaccines/administration & dosage/genetics/immunology Virion/genetics/immunology Visna-maedi virus
Group-specific antigen
Biolistics
biochemical phenomena
metabolism
and nutrition

Virology
Molecular biology
MESH: Male
MESH: Vaccines
DNA

MESH: T-Lymphocytes
gag/*genetics/immunology Immunization Male Pneumonia
biology.protein
Immunization
Epidermis
MESH: Epidermis
of Sheep/*prevention & control/virology Proviruses/isolation & purification Sheep T-Lymphocytes/immunology *Vaccines
MESH: Female
MESH: Antibodies
Viral
Zdroj: Vaccine
Vaccine, Elsevier, 2009, 27 (2), pp.260-9. ⟨10.1016/j.vaccine.2008.10.042⟩
Vaccine, 2009, 27 (2), pp.260-9. ⟨10.1016/j.vaccine.2008.10.042⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
ISSN: 0264-410X
DOI: 10.1016/j.vaccine.2008.10.042⟩
Popis: Niesalla, H. et al.
To determine whether systemic immunization with plasmid DNA and virus vector against visna/maedi virus (VMV) would induce protective immune responses, sheep were immunized with VMV gag and/or env sequences using particle-mediated epidermal bombardment and injection of recombinant modified vaccinia Ankara. The results showed that immunization induced both humoral and cell-mediated responses prior to and after virus challenge. The vaccination protocol did not prevent infection, but immunization with the gag gene or a combination of gag and env genes resulted in significantly reduced provirus loads in blood and mediastinal lymph node, respectively. Provirus loads in lung and draining lymph node were unaffected, but p25 expression was undetectable in lungs of animals immunized with a combination of gag and env genes. Analysis of target tissues for lesions at post-mortem showed that immunization with the env gene caused a significant increase in lesion score, while the gag gene or a combination of gag and env genes had no effect. Inclusion of the ovine interferon-γ gene in the initial priming mixture had minimal effect on immune responses, provirus load, or lesion development, although it resulted in a decreased p25 expression in the lung. The results thus show that systemic immunization with gag or a combination of gag and env genes reduces provirus load in blood and lymphoid tissue, respectively whereas env immunization has no effect on provirus load but increased lesion development. © 2008 Elsevier Ltd. All rights reserved.
This study was supported by grants from European Union (QLK2-CT-2002-00617) and Spanish CICYT (AGL2003-08977-C03-01 and AGL2007-66874-C04). Ramsés Reina and Ximena de Andrés were supported by a fellowship FPI from the Spanish Ministry of Science and Education. Tom McNeilly was supported by a PhD studentship from the Royal (Dick) College of Veterinary Studies, University of Edinburgh.
Databáze: OpenAIRE