A Partially Protective Vaccine for Fasciola hepatica Induced Degeneration of Adult Flukes Associated to a Severe Granulomatous Reaction in Sheep.
Verónica Molina-HernándezMaría T Ruiz-CampilloFrancisco Javier Martínez-MorenoLeandro BuffoniÁlvaro Martínez-MorenoRafael ZafraMaría J BautistaAlejandro EscamillaRaúl Pérez-CaballeroJosé PérezPublished in: Animals : an open access journal from MDPI (2021)
Fasciolosis is an important economic disease of livestock. There is a global interest in the development of protective vaccines since current anthelmintic therapy is no longer sustainable. A better knowledge of the host-parasite interaction is needed for the design of effective vaccines. The present study evaluates the microscopical hepatic lesions in sheep immunized with a partially protective vaccine (VAC1), a non-protective vaccine (VAC2), and an infected control group (IC). The nature of granulomatous inflammation associated with degeneration of adult flukes found in the VAC1 group was characterized by immunohistochemistry. Hepatic lesions (fibrous perihepatitis, chronic tracts, bile duct hyperplasia, infiltration of eosinophils and lymphocytes and plasma cells) were significantly less severe in the VAC1 group than in the IC group. Dead adult flukes within bile ducts were observed only in the VAC1 group and were surrounded by a severe granulomatous inflammation composed by macrophages and multinucleate giant cells with a high expression of lysozyme, CD163 and S100 markers, and a low expression of CD68. Numerous CD3+ T lymphocytes and scarce infiltrate of FoxP3+ Treg and CD208+ dendritic cells were present. This is the first report describing degenerated flukes associated to a severe granulomatous inflammation in bile ducts in a F. hepatica vaccine trial.
Keyphrases
- oxidative stress
- induced apoptosis
- dendritic cells
- early onset
- poor prognosis
- drug induced
- cell cycle arrest
- interstitial lung disease
- regulatory t cells
- nk cells
- healthcare
- cell proliferation
- long non coding rna
- peripheral blood
- endothelial cells
- study protocol
- signaling pathway
- mesenchymal stem cells
- cell death
- smoking cessation
- electron transfer