
doi: 10.2741/2166
pmid: 17127400
The ovine maedi-visna virus (MVV) was the first lentivirus to be isolated and characterized 1957 in Iceland. MVV leads to a life-long, persistent infection with slow development of lesions in the lung and the central nervous system (CNS). The main target cells of MVV are of the monocyte/macrophage lineage and it does not infect T-lymphocytes or cause immune suppression like human immune deficiency virus (HIV). In spite of a fairly good immune response, including both neutralizing antibodies and cytotoxic T lymphocytes, the virus persists in the host and establishes a life-long infection. There are strong indications that the pathological lesions are immune-mediated and vaccination attempts have not only failed to induce sterile immunity but have occasionally caused increased viremia and more severe disease.
Immunity, Cellular, Visna, Sheep, Visna-maedi virus, Pneumonia, Progressive Interstitial, of Sheep, Antibody Formation, Animals, Viral Vaccines
Immunity, Cellular, Visna, Sheep, Visna-maedi virus, Pneumonia, Progressive Interstitial, of Sheep, Antibody Formation, Animals, Viral Vaccines
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