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Dissertation
Contribution à la caractérisation de la réponse immune dirigée contre les glycoprotéines d'enveloppe du virus de la leucémie bovine (BLV).
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Year: 1992

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Dissertation
Etude du rôle des sites de N-glycosylation dans la pathogenèse induite par le virus de la leucémie bovine
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Year: 2014

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Article
Protective effects of a live attenuated bovine leukaemia virus vaccine with deletion in the R3 and G4 genes.
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Year: 2000 Publisher: [S.l.] : [s.n.],

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Article
Role of the proline-rich motif of bovine leukemia virus transmembrane protein gp30 in viral load and pathogenicity in sheep.
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Year: 2001 Publisher: [S.l.] : [s.n.],

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Dissertation
Potentiel infectieux de virus BLV mutés dans les sites de glycosylation de l'enveloppe virale
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Year: 2011 Publisher: [S.l. : chez l'auteur],

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Dissertation
Analyse de la variabilité génétique du virus de la leucémie bovine.
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Year: 1992

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Article
Inhibition of histone deacetylases induces bovine leukemia virus expression in vitro and in vivo.
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Year: 2002 Publisher: [S.l.] : [s.n.],


Dissertation
Establishment of a cell line for the production of vaccine against bovine leukaemia virus
Authors: --- --- --- --- --- et al.
Year: 2022 Publisher: Liège Université de Liège (ULiège)

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Bovine Leukaemia Virus (BLV) is a retrovirus that infect cattle, yak, water buffalo and zebu. The most common manifestation of the virus is an accumulation of infected B lymphocytes called persistent lymphocytosis (PL). This virus is present all over the world except in western Europe where a large campaign of testing and euthanasia of infected animals has been conducted. BLV economic impact is estimated at US$525 million due to a loss of milk production but also to a shorter animal lifespan. Preventive actions implemented to limit the spread of the virus often fail due to a lack of commitment to the programme. Therefore, a vaccine is urgently needed to facilitate herd management and disease control. A safe and effective vaccine based on an attenuated BLV strain (pBLV6073DX) has recently been developed. However, the current inoculation technique based on purified DNA does not allow for large-scale vaccination. In this context, the objective of this master thesis is to obtain a cell line expressing the vaccine strain in order to consider its larger-scale production. For this purpose, Vero cells were either transfected with the proviral insert or transduced with viral particles. After sorting with a flow cytometer and PCR-based clone selection, a cell line having stably integrated the vaccine sequence was isolated. Inoculation of sheep with this cell line effectively transmitted the vaccine strain, providing the proof-of-concept of the approach.

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