AniCura Istituto Veterinario di Novara, Strada Provinciale 9, 28060 Granozzo con Monticello (NO), Italy.
Department of Animal Medicine, Production and Health, University of Padova, viale dell'Università 16, 35020 Legnaro (PD), Italy.
Viruses. 2020 Jun 12;12(6):640. doi: 10.3390/v12060640.
Feline parvovirus (FPV) causes severe gastroenteritis and leukopenia in cats; the outcome is poor. Information regarding specific treatments is lacking. Class A CpG oligodeoxynucleotides (CpG-A) are short single-stranded DNAs, stimulating type I interferon production. In cats, CpG-A induced an antiviral response in vivo and inhibited FPV replication in vitro. The aim was to prospectively investigate the effects of CpG-A on survival, clinical score, hematological findings, antiviral response (cytokines), viremia, and fecal shedding (real-time qPCR) in cats naturally infected with FPV. Forty-two FPV-infected cats were randomized to receive 100 µg/kg of CpG-A ( = 22) or placebo ( = 20) subcutaneously, on admission and after 48 h. Blood and fecal samples were collected on admission, after 1, 3, and 7 days. All 22 cats showed short duration pain during CpG-A injections. The survival rate, clinical score, leukocyte and erythrocyte counts, viremia, and fecal shedding at any time-point did not differ between cats treated with CpG-A (50%) and placebo (40%). Antiviral myxovirus resistance () gene transcription increased in both groups from day 1 to 3 ( = 0.005). Antibodies against FPV on admission were associated with survival in cats ( = 0.002). In conclusion, CpG-A treatment did not improve the outcome in cats with FPV infection. FPV infection produced an antiviral response.
猫细小病毒(FPV)可引起猫严重的胃肠炎和白细胞减少症,预后不良。缺乏针对特定治疗方法的信息。A 类 CpG 寡脱氧核苷酸(CpG-A)是短的单链 DNA,可刺激 I 型干扰素的产生。在猫中,CpG-A 可在体内诱导抗病毒反应并抑制 FPV 的体外复制。本研究旨在前瞻性调查 CpG-A 对自然感染 FPV 的猫的存活率、临床评分、血液学发现、抗病毒反应(细胞因子)、病毒血症和粪便脱落(实时 qPCR)的影响。42 只 FPV 感染的猫随机分为皮下注射 100 µg/kg 的 CpG-A(n = 22)或安慰剂(n = 20),分别在入院时和 48 小时后注射。入院时、第 1、3 和 7 天采集血液和粪便样本。在接受 CpG-A 治疗的 22 只猫中,有 22 只在注射过程中均出现短暂的疼痛。接受 CpG-A 治疗的猫(50%)和安慰剂(40%)的存活率、临床评分、白细胞和红细胞计数、病毒血症和粪便脱落率在任何时间点均无差异。两组的抗病毒(myxovirus resistance )基因转录均从第 1 天增加到第 3 天( = 0.005)。入院时针对 FPV 的抗体与猫的存活率相关( = 0.002)。总之,CPG-A 治疗不能改善 FPV 感染猫的预后。FPV 感染产生了抗病毒反应。