Mackin Andrew J, Riggs Caitlin, Beatty Todd, Mealey Katrina, Boothe Dawn, Archer Todd
From Mississippi State University College of Veterinary Medicine, Starkville, Mississippi (A.J.M., C.R., T.A.); Garden Grove Animal Hospital, Winter Haven, Florida (T.B.); Washington State University College of Veterinary Medicine, Pullman, Washington (K.M.); and Auburn University College of Veterinary Medicine, Auburn, Alabama (D.B.).
J Am Anim Hosp Assoc. 2020 May/Jun;56(3):190. doi: 10.5326/JAAHA-MS-7004. Epub 2020 Mar 17.
Pharmacodynamic monitoring was used to titrate cyclosporine dosing in a dog with immune-mediated hemolytic anemia. Development of a suspected secondary infection, with subsequent discovery of an unexpectedly high level of T-cell suppression despite a relatively low cyclosporine dose, prompted an investigation into the cause of possible excessive immunosuppression. Blood cyclosporine concentrations were within expected target ranges, and the dog was determined to be heterozygous for the multidrug resistance protein 1 (MDR1; ATP-binding cassette sub family B member 1-1Δ) gene mutation. The MDR1 mutation was suspected to have contributed to the excessive immunosuppression experienced by this patient. This case highlights the need to monitor immunosuppressive therapy in the individual patient, especially when the patient is not responding to therapy at typical dosages or when secondary infections develop at dosages lower than expected to cause significant immunosuppression. Pharmacodynamic monitoring can be used to help identify unexpected excessive immunosuppression in dogs receiving cyclosporine, and MDR1 genotyping should be further explored as a potential method of predicting and preventing its occurrence.
采用药效学监测来调整一只患有免疫介导性溶血性贫血犬的环孢素剂量。出现疑似继发感染,随后发现尽管环孢素剂量相对较低,但T细胞抑制水平却意外地高,这促使对可能过度免疫抑制的原因进行调查。血液中环孢素浓度在预期目标范围内,且该犬被确定为多药耐药蛋白1(MDR1;ATP结合盒亚家族B成员1-1Δ)基因突变的杂合子。怀疑MDR1突变导致了该患者出现过度免疫抑制。该病例凸显了对个体患者免疫抑制治疗进行监测的必要性,尤其是当患者对典型剂量的治疗无反应或在低于预期导致显著免疫抑制的剂量下发生继发感染时。药效学监测可用于帮助识别接受环孢素治疗的犬中意外的过度免疫抑制,并且MDR1基因分型应作为预测和预防其发生的潜在方法进行进一步探索。