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Peer-reviewed veterinary case report

Treatment options for canine visceral leishmaniasis compared in dogs

By Cardoso, Jamille Mirelle de Oliveira et al.·Published in Molecular immunology·2022·Laborat&#xf3, Brazil·View original on PubMed

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Original publication title: Comparative evaluation of meglumine antimoniate encapsulated in a mixture of conventional and PEGylated liposomes and immunotherapy using an anti-canine IL-10 receptor-blocking monoclonal antibody on canine visceral leishmaniasis.

Species:
dog

Plain-English summary

Twenty mongrel dogs with canine visceral leishmaniasis (CVL), a serious infection caused by the Leishmania parasite, were treated with either a chemotherapy drug called meglumine antimoniate or an immunotherapy using a special antibody. The dogs received either six doses of the chemotherapy or two doses of the immunotherapy. Both treatments showed initial improvements in the dogs' health and immune response, but these benefits did not last long-term. Researchers suggest that combining both treatments or giving booster doses may help improve the effectiveness of treating CVL in dogs.

People also search for: dog leishmaniasis treatment · canine visceral leishmaniasis symptoms · meglumine antimoniate for dogs · immunotherapy for dog infections

Abstract

This study compared the therapeutic potential of the chemotherapy using meglumine antimoniate encapsulated in a mixture of conventional and PEGylated liposomes (Nano Sb) and immunotherapy with anti-canine IL-10 receptor-blocking monoclonal antibody (Anti IL-10R) on canine visceral leishmaniasis (CVL). Twenty mongrel dogs naturally infected by L. infantum, displaying clinical signs of visceral leishmaniasis were randomly divided in two groups. In the first one, nine dogs received six intravenous doses of a mixture of conventional and PEGylated liposomes containing meglumine antimoniate at 6.5 mg Sb/kg/dose. In the second one, eleven dogs received two intramuscular doses of 4 mg of anti-canine IL-10 receptor-blocking monoclonal antibody. The animals were evaluated before (T0) and 30, 90, and 180 days after treatments. Our major results demonstrated that both treatments were able to maintain hematological and biochemical parameters, increase circulating T lymphocytes subpopulations, increase the IFN-γ producing T-CD4 lymphocytes, restore the lymphoproliferative capacity and improve the clinical status. However, although these improvements were observed in the initial post-treatment times, they did not maintain until the end of the experimental follow-up. We believe that the use of booster doses or the association of chemotherapy and immunotherapy (immunochemotherapy) is promising to improve the effectiveness of treating CVL for improving the clinical signs and possibly reducing the parasite burden in dogs infected with Leishmania infantum.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/34814056/