Prophylactic use of canine parvovirus monoclonal antibody induces blockade of vaccinal canine parvovirus immunization similar to maternally derived passive immunity.

IF 1.4 3区 农林科学 Q2 VETERINARY SCIENCES
Laurie Larson, Jason Hansen, Prakash Ramasami, Jennifer M Miller, Barton J Slagter, Danielle Tremblay, Mayur Patel, Terri Wasmoen
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引用次数: 0

Abstract

Objective: To determine initial antibody titer, degradation profile, and duration of passive antibody blockade of active immunization by modified-live viral (MLV) canine parvovirus (CPV-2) vaccine following CPV monoclonal antibody (CPMA) prophylactic subcutaneous (SC) administration to CPV-2-naïve puppies.

Methods: Purpose-bred, CPV-2-seronegative male and female Beagle dogs, 7 to 8 weeks of age, were randomized to CPMA treatment (n = 13) and control (7) groups. Dogs were commingled and group housed in a shower-in/shower-out facility. At study day 0, dogs were administered either 0.1 mL/kg body weight CPMA SC or an equivalent volume of saline. Sera collected weekly over 140 days were assayed via hemagglutination inhibition and serum virus neutralization. All dogs were administered a commercially available MLV vaccine containing CPV-2 in combination with other core vaccine viruses at 3-week time points beginning at study day 42.

Results: All control dogs remained seronegative through day 42 and seroconverted to CPV-2 after the initial dose of MLV vaccine. By study day 1, the CPMA-treated group showed a mean passive hemagglutination inhibition titer of 1,674. The average degradation rate was calculated at R2 = 0.97, with a mean half-life of 18.9 days. Twelve of 13 (92%) in the treated group seroconverted after a fourth vaccination on day 105.

Conclusions: Prophylactic CPMA at 0.1 mL/kg body weight SC can block active CPV-2 immunization for 15 weeks when given to seronegative puppies.

Clinical relevance: Initial puppy vaccination series should be extended after CPMA prophylactic use.

预防性使用犬细小病毒单克隆抗体可诱导阻断犬细小病毒疫苗免疫,类似于母源性被动免疫。
目的:通过对CPV-2-naïve幼犬进行CPV单克隆抗体(CPMA)预防性皮下注射,测定修饰活病毒(MLV)犬细小病毒(CPV-2)疫苗主动免疫后的初始抗体滴度、降解谱和被动抗体阻断时间。方法:选择7 ~ 8周龄、目的种、cpv -2血清阴性的公母Beagle犬,随机分为CPMA治疗组(n = 13)和对照组(n = 7)。狗被混合在一起,并被集体安置在一个淋浴/淋浴设施中。在研究第0天,狗被给予0.1 mL/kg体重的CPMA SC或等量的生理盐水。每周收集140天的血清,通过血凝抑制和血清病毒中和进行检测。在研究第42天开始的3周时间点,所有狗都接种了含有CPV-2和其他核心疫苗病毒的市售MLV疫苗。结果:所有对照犬在第42天保持血清阴性,并在初始剂量接种后血清转化为CPV-2。在研究第1天,cpma治疗组的平均被动血凝抑制效价为1674。平均降解率R2 = 0.97,平均半衰期为18.9天。治疗组13人中有12人(92%)在第105天接种第四次疫苗后血清转化。结论:0.1 mL/kg体重SC的预防性CPMA可阻断CPV-2活性免疫15周。临床相关性:在CPMA预防性使用后,初始幼犬接种系列应延长。
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来源期刊
CiteScore
1.70
自引率
10.00%
发文量
186
审稿时长
3 months
期刊介绍: The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.
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