Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich, Munich, Germany.
Clinical Laboratory, Department of Clinical Diagnostics and Services, Center for Clinical Studies, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
J Feline Med Surg. 2023 Aug;25(8):1098612X231183250. doi: 10.1177/1098612X231183250.
Feline infectious peritonitis (FIP), a common disease in cats caused by feline coronavirus (FCoV), is usually fatal once clinical signs appear. Successful treatment of FIP with oral GS-441524 for 84 days was demonstrated recently by this research group. The aim of this study was to evaluate the long-term outcome in these cats.
A total of 18 successfully treated cats were followed for up to 1 year after treatment initiation (9 months after completion of the antiviral treatment). Follow-up examinations were performed at 12-week intervals, including physical examination, haematology, serum biochemistry, abdominal and thoracic ultrasound, FCoV ribonucleic acid (RNA) loads in blood and faeces by reverse transciptase-quantitative PCR and anti-FCoV antibody titres by indirect immunofluorescence assay.
Follow-up data were available from 18 cats in week 24, from 15 cats in week 36 and from 14 cats in week 48 (after the start of treatment), respectively. Laboratory parameters remained stable after the end of the treatment, with undetectable blood viral loads (in all but one cat on one occasion). Recurrence of faecal FCoV shedding was detected in five cats. In four cats, an intermediate short-term rise in anti-FCoV antibody titres was detected. In total, 12 cats showed abdominal lymphadenomegaly during the follow-up period; four of them continuously during the treatment and follow-up period. Two cats developed mild neurological signs, compatible with feline hyperaesthesia syndrome, in weeks 36 and 48, respectively; however, FCoV RNA remained undetectable in blood and faeces, and no increase in anti-FCoV antibody titres was observed in these two cats, and the signs resolved.
Treatment with GS-441524 proved to be effective against FIP in both the short term as well as the long term, with no confirmed relapse during the 1-year follow-up period. Whether delayed neurological signs could be a long-term adverse effect of the treatment or associated with a 'long FIP syndrome' needs to be further evaluated.
猫传染性腹膜炎(FIP)是一种由猫冠状病毒(FCoV)引起的猫科动物常见疾病,一旦出现临床症状通常是致命的。本研究小组最近证明,口服 GS-441524 治疗 FIP 可取得 84 天的成功。本研究的目的是评估这些猫的长期预后。
18 只成功治疗的猫在开始治疗后最长随访 1 年(抗病毒治疗完成后 9 个月)。每隔 12 周进行一次随访检查,包括体格检查、血常规、血清生化、腹部和胸部超声、血液和粪便中 FCoV 核糖核酸(RNA)的逆转录定量聚合酶链反应(RT-qPCR)和间接免疫荧光法检测抗 FCoV 抗体滴度。
分别在第 24 周、第 36 周和第 48 周(治疗开始后)获得了 18 只猫的随访数据。治疗结束后,实验室参数保持稳定,除一只猫在一次检测中血液病毒载量无法检测到(all but one cat on one occasion)。5 只猫粪便中再次检测到 FCoV 脱落。4 只猫的抗 FCoV 抗体滴度在中期短暂升高。总共有 12 只猫在随访期间出现腹部淋巴结肿大;其中 4 只猫在治疗和随访期间持续肿大。2 只猫分别在第 36 周和第 48 周出现轻度神经症状,符合猫超敏综合征;然而,在这两只猫的血液和粪便中均未检测到 FCoV RNA,并且在这两只猫中未观察到抗 FCoV 抗体滴度升高,症状也得到了缓解。
GS-441524 的治疗在短期和长期内均对 FIP 有效,在 1 年的随访期间未确认复发。神经症状延迟是否是治疗的长期不良反应,还是与“长 FIP 综合征”有关,需要进一步评估。