Key result
T-lymphocyte suppression and interfering aMPV-B vaccine exposure were associated with considerable variation in aMPV-A vaccine replication, clinical signs, and protection against challenge in turkeys.
T-lymphocyte suppression and prior interfering vaccine exposure may explain the variable protection provided by aMPV vaccines in turkeys under field conditions.
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T-cell suppression and aMPV-B interference may underlie inconsistent aMPV vaccine performance in field turkeys; hypothesis-generating for immunomodulation strategies.
Avian metapneumovirus (aMPV) is an important respiratory pathogen of turkeys with considerable economic impact on poultry production. Although vaccination is widely used for the control of the disease, questions regarding vaccine safety and efficacy remain to be elucidated. This report describes the problems associated with reproducibility of the aMPV-vaccine response, comparing T-lymphocyte-compromised and T-cell-intact turkeys. In three consecutive experiments, turkeys partially depleted of T-lymphocytes by treatment with cyclosporin A as well as untreated turkeys were vaccinated with a commercial live aMPV subtype A (aMPV-A) vaccine at 2 weeks of age. Two weeks later they were challenged with a virulent aMPV-A strain. Despite similar genetic background of the turkeys, comparable housing conditions under isolation and the application of the same aMPV-A vaccine, considerable variation was observed among the experiments regarding replication of the vaccine virus, vaccine-induced clinical signs and protection against challenge infection. The results indicate that differences in the outcome of aMPV-A vaccination may be associated with T-lymphocyte suppression and additionally with an interfering aMPV-B vaccine exposure at the hatchery in two of the experiments. Our study provides possible explanations for the variable protection provided by aMPV vaccines under field conditions.
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Rubbenstroth et al. (2010) studied Avian metapneumovirus (aMPV). T-lymphocyte depletion by cyclosporin A vs. untreated turkeys was evaluated on Replication of the vaccine virus, vaccine-induced clinical signs and protection against challenge infection. T-lymphocyte suppression and interfering aMPV-B vaccine exposure were associated with considerable variation in aMPV-A vaccine replication, clinical signs, and protection against challenge in turkeys.
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