Aviso: para depositar documentos, por favor, inicia sesión e identifícate con tu cuenta de correo institucional de la UCM con el botón MI CUENTA UCM. No emplees la opción AUTENTICACIÓN CON CONTRASEÑA
 

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

dc.contributor.authorBaxarias, Marta
dc.contributor.authorDonato, Giulia
dc.contributor.authorMateu, Cristina
dc.contributor.authorSalichs, Marta
dc.contributor.authorHomedes, Josep
dc.contributor.authorMiró Corrales, Guadalupe
dc.contributor.authorPennisi, Maria Grazia
dc.contributor.authorSolano Gallego, Laia
dc.date.accessioned2024-05-24T16:33:52Z
dc.date.available2024-05-24T16:33:52Z
dc.date.issued2023-10-04
dc.description2023 Acuerdos transformativos CRUE
dc.description.abstractBackground: 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 Dogs that developed disease were withdrawn from the study and classified as sick dogs.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.
dc.description.departmentDepto. de Sanidad Animal
dc.description.facultyFac. de Veterinaria
dc.description.fundingtypeAPC financiada por la UCM
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationBaxarias, M., Donato, G., Mateu, C. et al. 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. Parasites Vectors 16, 344 (2023). https://doi.org/10.1186/s13071-023-05903-0
dc.identifier.doi10.1186/s13071-023-05903-0
dc.identifier.essn1756-3305
dc.identifier.officialurlhttps://doi.org/10.1186/s13071-023-05903-0
dc.identifier.pmid37794502
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/37794502/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/104425
dc.issue.number344
dc.journal.titleParasites & Vectors
dc.language.isoeng
dc.publisherSpringer
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu636.7.09:616
dc.subject.keywordAntibody
dc.subject.keywordCanine
dc.subject.keywordDomperidone
dc.subject.keywordInterferon gamma
dc.subject.keywordLeishmaniosis
dc.subject.keywordPCR
dc.subject.keywordPlacebo
dc.subject.ucmVeterinaria
dc.subject.unesco3109 Ciencias Veterinarias
dc.titleA 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
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number16
dspace.entity.typePublication
relation.isAuthorOfPublicationa2e597a9-b881-4e99-9faf-b56b882afe90
relation.isAuthorOfPublication.latestForDiscoverya2e597a9-b881-4e99-9faf-b56b882afe90

Download

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
s13071-023-05903-0.pdf
Size:
1.52 MB
Format:
Adobe Portable Document Format
Description:
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

Collections