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A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs

BACKGROUND: Domperidone (Leisguard(®)) is an immunomodulatory drug used as a preventive measure in healthy dogs. However, no studies have been published in healthy Leishmania infantum-seropositive dogs. The aim of this study was to evaluate the clinical efficacy and safety of domperidone as immunoth...

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Autores principales: Baxarias, Marta, Donato, Giulia, Mateu, Cristina, Salichs, Marta, Homedes, Josep, Miró, Guadalupe, Pennisi, Maria Grazia, Solano-Gallego, Laia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552330/
https://www.ncbi.nlm.nih.gov/pubmed/37794502
http://dx.doi.org/10.1186/s13071-023-05903-0
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author Baxarias, Marta
Donato, Giulia
Mateu, Cristina
Salichs, Marta
Homedes, Josep
Miró, Guadalupe
Pennisi, Maria Grazia
Solano-Gallego, Laia
author_facet Baxarias, Marta
Donato, Giulia
Mateu, Cristina
Salichs, Marta
Homedes, Josep
Miró, Guadalupe
Pennisi, Maria Grazia
Solano-Gallego, Laia
author_sort Baxarias, Marta
collection PubMed
description BACKGROUND: Domperidone (Leisguard(®)) is an immunomodulatory drug used as a preventive measure in healthy dogs. However, no studies have been published in healthy Leishmania infantum-seropositive dogs. The aim of this study was to evaluate the clinical efficacy and safety of domperidone as immunotherapy in Leishmania-seropositive healthy dogs. METHODS: Sixty-seven dogs were treated with domperidone at 0.5 mg/kg and 44 dogs received placebo, once daily for 4 consecutive weeks. Monthly treatments were repeated every 4 months until the end of the 1-year follow-up period. Veterinary examinations were performed on days 0, 30, 120, 150, 240, 270 and 360. Samples of blood and urine were collected on days 0, 120, 240 and 360 for routine laboratory tests and quantitative in-house ELISA for the detection of L. infantum-specific antibodies. Furthermore, Leishmania real-time PCR and IFN-γ ELISA were performed at day 0 and the end of the study. Dogs that developed disease were withdrawn from the study and classified as sick dogs. Adverse drug reactions were reported. RESULTS: Thirty dogs developed disease during the follow-up period: 13/67 (19.4%) in the group treated with domperidone and 17/44 (38.6%) in the placebo-treated group (P = 0.03). Low-seropositive dogs treated with domperidone (4/40, 9.1%) were significantly less likely to develop disease compared to low-seropositive dogs treated with placebo (7/24, 29.2%; P = 0.04), while no differences were found between domperidone (9/23, 39.1%) and placebo (10/20, 50%) in medium- to high-seropositive dogs. At the end of the study, a higher proportion of Leishmania PCR-positive dogs was observed in the placebo-treated group (16/33, 48.5%) compared to the domperidone group (13/51, 25.5%; P = 0.04). Furthermore, low-seropositive dogs treated with domperidone with an increase of IFN-γ concentration presented a higher increase than those treated with placebo at the end of the study. Four dogs treated with domperidone presented self-limiting diarrhea. CONCLUSIONS: Healthy dogs with low L. infantum antibody levels treated with domperidone were less likely to develop disease compared to placebo-treated dogs. Furthermore, domperidone presented a good safety profile. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-023-05903-0.
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spelling pubmed-105523302023-10-06 A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs Baxarias, Marta Donato, Giulia Mateu, Cristina Salichs, Marta Homedes, Josep Miró, Guadalupe Pennisi, Maria Grazia Solano-Gallego, Laia Parasit Vectors Research BACKGROUND: Domperidone (Leisguard(®)) is an immunomodulatory drug used as a preventive measure in healthy dogs. However, no studies have been published in healthy Leishmania infantum-seropositive dogs. The aim of this study was to evaluate the clinical efficacy and safety of domperidone as immunotherapy in Leishmania-seropositive healthy dogs. METHODS: Sixty-seven dogs were treated with domperidone at 0.5 mg/kg and 44 dogs received placebo, once daily for 4 consecutive weeks. Monthly treatments were repeated every 4 months until the end of the 1-year follow-up period. Veterinary examinations were performed on days 0, 30, 120, 150, 240, 270 and 360. Samples of blood and urine were collected on days 0, 120, 240 and 360 for routine laboratory tests and quantitative in-house ELISA for the detection of L. infantum-specific antibodies. Furthermore, Leishmania real-time PCR and IFN-γ ELISA were performed at day 0 and the end of the study. Dogs that developed disease were withdrawn from the study and classified as sick dogs. Adverse drug reactions were reported. RESULTS: Thirty dogs developed disease during the follow-up period: 13/67 (19.4%) in the group treated with domperidone and 17/44 (38.6%) in the placebo-treated group (P = 0.03). Low-seropositive dogs treated with domperidone (4/40, 9.1%) were significantly less likely to develop disease compared to low-seropositive dogs treated with placebo (7/24, 29.2%; P = 0.04), while no differences were found between domperidone (9/23, 39.1%) and placebo (10/20, 50%) in medium- to high-seropositive dogs. At the end of the study, a higher proportion of Leishmania PCR-positive dogs was observed in the placebo-treated group (16/33, 48.5%) compared to the domperidone group (13/51, 25.5%; P = 0.04). Furthermore, low-seropositive dogs treated with domperidone with an increase of IFN-γ concentration presented a higher increase than those treated with placebo at the end of the study. Four dogs treated with domperidone presented self-limiting diarrhea. CONCLUSIONS: Healthy dogs with low L. infantum antibody levels treated with domperidone were less likely to develop disease compared to placebo-treated dogs. Furthermore, domperidone presented a good safety profile. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-023-05903-0. BioMed Central 2023-10-04 /pmc/articles/PMC10552330/ /pubmed/37794502 http://dx.doi.org/10.1186/s13071-023-05903-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Baxarias, Marta
Donato, Giulia
Mateu, Cristina
Salichs, Marta
Homedes, Josep
Miró, Guadalupe
Pennisi, Maria Grazia
Solano-Gallego, Laia
A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs
title A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs
title_full A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs
title_fullStr A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs
title_full_unstemmed A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs
title_short A blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of Leisguard(®) as an immunotherapeutic treatment for healthy Leishmania infantum-seropositive dogs
title_sort blinded, randomized and controlled multicenter clinical trial to assess the efficacy and safety of leisguard(®) as an immunotherapeutic treatment for healthy leishmania infantum-seropositive dogs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552330/
https://www.ncbi.nlm.nih.gov/pubmed/37794502
http://dx.doi.org/10.1186/s13071-023-05903-0
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