Efficacy of a Bruton's Tyrosine Kinase Inhibitor (PRN‐473) in the treatment of canine pemphigus foliaceus
Background Bruton's tyrosine kinase (BTK) is important in B‐cell signalling. Efficacy has been reported for BTK inhibitors (BTKi) in human autoimmune diseases. Canine pemphigus foliaceus (cPF) is the most common canine autoimmune skin disease. Objectives To determine the safety and efficacy of...
Gespeichert in:
Veröffentlicht in: | Veterinary dermatology 2020-08, Vol.31 (4), p.291-e71 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background
Bruton's tyrosine kinase (BTK) is important in B‐cell signalling. Efficacy has been reported for BTK inhibitors (BTKi) in human autoimmune diseases. Canine pemphigus foliaceus (cPF) is the most common canine autoimmune skin disease.
Objectives
To determine the safety and efficacy of a BTKi in cPF treatment.
Animals
Nine privately owned dogs.
Methods and materials
Nine dogs diagnosed with PF were administered BTKi PRN473. Initial dosages were ≈15 mg/kg once daily, increased to twice daily if inadequate response was seen. Treatment continued for a maximum of 20 weeks, attempting decrease to every other day. Dogs were monitored with complete blood counts, serum biochemistry panels, urinalyses and evaluated with a modified version of a validated human Pemphigus Disease Activity Index (cPDAI). Anti‐desmocollin‐1 (DSC‐1) and desmoglein‐1 (DSG‐1) immunoglobulin G (IgG) titres were performed before and after the treatment period. Drug bound to target was measured in peripheral blood mononuclear cells.
Results
All nine dogs showed reduction in lesions and cPDAI score during the first two weeks of treatment. At the end of the study, four responses were considered “good”, two “fair”, two “poor” and one dog withdrawn due to recurrence of a previously excised mast cell tumour. Four dogs continued to improve by Week 4; three sustained near complete remission by study's end. The anti‐DSC‐1 IgG titre decreased in three dogs, increased in two, was undetected in three and was not performed in the withdrawn dog. No dogs had detectable IgG to DSG1. Possible adverse effects occurred in three dogs.
Conclusions and clinical importance
Bruton's tyrosine kinase inhibitor monotherapy may have beneficial effects in some cases of cPF.
RésuméContexteLa BTK (Bruton's tyrosine kinase) est une voie importante d'activation des cellules B. L'efficacité a été rapportée pour les inhibiteurs de BTK (BTKi) dans les maladies auto‐immunes de l'homme. Le pemphigus foliacé du chien (cPF) est la dermatite auto‐immune la plus fréquente du chien.ObjectifsDéterminer l'efficacité et l'innocuité d'un BTKi dans le traitement d'un cPF.SujetsNeufs chiens de propriétaires.Matériels et méthodesNeuf chiens diagnostiqués avec PF ont reçu du BTKi PRN473. Les doses initiales étaient ≈15 mg/kg une fois par jour, augmenté à deux fois par jour si une réponse inadéquate était observée. Le traitement était poursuivi au maximum 20 semaines, tentant de réduire à jours alternés. Les chiens étaient monitorés p |
---|---|
ISSN: | 0959-4493 1365-3164 |
DOI: | 10.1111/vde.12841 |