Medical Journals

Vaccination of Sheep with Maedi-visna Virus Gag Gene and Protein, Beneficial or Harmful?

Authors:
  • Torsteinsdóttir Sigurbjörg
  • Carlsdóttir Helga María
  • Svansson Vilhjálmur
  • Matthíasdóttir Sigrídur
  • Martin Agnes Helga
  • Pétursson Gudmundur

From: Institute for Experimental Pathology, University of Iceland, Keldur v/Vesturlandsveg, IS-112 Reykjavík, Iceland. sibbath@hi.is

Vaccine

  • Publish Date: Sep 2007
  • ISSN: 0264-410X
  • Volume: 25
  • Issue: 37-38
  • Pages: 6713-20
  • Medium: Print
  • Language: English
  • Citation (JAMA): Torsteinsdóttir Sigurbjörg, Carlsdóttir Helga María, Svansson Vilhjálmur, et al. Vaccination of Sheep with Maedi-visna Virus Gag Gene and Protein, Beneficial or Harmful?. Vaccine Sep 2007;25:6713-20

Abstract

In spite of intense efforts no vaccine is yet available that protects against lentiviral infections. Sheep were immunised eight times over a period of 2.5 years with the maedi-visna (MVV) gag gene on two different vectors, 2 sheep with VR1012-gag-CTE and 2 sheep with pcDNA3.1-gag-CTE. All sheep responded to some of the mature MVV Gag proteins in Western blot (WB). Three of them responded to the virus in lymphocyte proliferation test. The sheep received a boost with recombinant Gag protein resulting in elevated antibody response. However, when they were challenged intratracheally with MVV they all became immediately infected as judged by a strong rise in antibody titer and virus isolation from blood. It is therefore clear that the vaccination gave no protection. It is even possible that it facilitated infectivity since virus was isolated earlier from all the vaccinated sheep than from any of the unvaccinated sheep infected in the same way with the same dose.

Mesh Headings (Keywords): Animals, Antibodies, Viral, Cell Line, Cell Proliferation, Cells, Cultured, Cercopithecus aethiops, DNA, Viral, Enzyme-Linked Immunosorbent Assay, Female, Gene Products, gag, Immunization, Lymphocytes, Sheep, Time Factors, Vaccination, Visna-maedi virus


Check for Full Text / PubMed Unique Identifier (PMID): 17686553


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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