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一种四价犬钩端螺旋体病疫苗中格氏疏螺旋体血清型成分的15个月免疫持续时间。

Fifteen-month duration of immunity for the serovar Grippotyphosa fraction of a tetravalent canine leptospirosis vaccine.

作者信息

Grosenbaugh Deborah A, Pardo Maria Camila

机构信息

Boehringer Ingelheim Animal Health, Athens, Georgia, USA.

Animal Health Industry Consultant, Athens, Georgia, USA.

出版信息

Vet Rec. 2018 Jun 9;182(23):665. doi: 10.1136/vr.104694. Epub 2018 Feb 19.

DOI:10.1136/vr.104694
PMID:29459489
Abstract

Forty-four specific pathogen-free beagles, median age 65 days, received two subcutaneous doses of either a commercially available, five-way combination vaccine or the same vaccine in combination with a tetravalent bacterin (Canicola, Grippotyphosa, Icterohaemorrhagiae, Pomona). They were subsequently challenged with a pathogenic strain serovar Grippotyphosa 470 days following completion of the vaccination protocol. Titres of agglutinating serum antibodies were determined at various time points before and after both vaccination and challenge, along with postchallenge reisolation of the challenge organisms from blood and urine, and evaluation of renal histopathology. Clinical signs of generalised leptospirosis were not observed in any of the dogs after challenge. In order to demonstrate efficacy, leptospirosis was defined as having at least one positive urine sample and a positive renal histopathology score; or, in the absence of renal pathology, multiple positive urine samples. Leptospiremia was not demonstrated in any of the vaccinated dogs versus 27 per cent of the controls; leptospiruria was noted in 5 per cent of the vaccinates compared with 76 per cent of controls; and renal lesions were observed in 15 per cent of the vaccinates and 65 per cent controls. Using these criteria, the vaccine was able to significantly prevent leptospirosis (P=0.0001) in the vaccinated animals. This study establishes duration of immunity of at least 15 months for the prevention of disease and renal excretion of leptospires for the serovar Grippotyphosa fraction of a quadrivalent vaccine.

摘要

44只特定病原体-free比格犬,中位年龄65天,接受了两剂皮下注射,分别为市售的五联疫苗或该疫苗与四价菌苗(犬型、黄疸出血型、波摩那型、流感伤寒型)的联合疫苗。在完成疫苗接种方案470天后,它们随后受到致病性血清型流感伤寒型菌株的攻击。在接种疫苗和攻击前后的不同时间点测定凝集血清抗体滴度,同时从血液和尿液中对攻击后的病原体进行再分离,并评估肾脏组织病理学。攻击后,在任何一只犬中均未观察到全身性钩端螺旋体病的临床症状。为了证明疗效,钩端螺旋体病被定义为至少有一份尿液样本呈阳性且肾脏组织病理学评分呈阳性;或者,在没有肾脏病理学的情况下,有多份阳性尿液样本。与27%的对照组相比,任何一只接种疫苗的犬均未出现钩端螺旋体血症;接种疫苗的犬中有5%出现钩端螺旋体尿,而对照组为76%;接种疫苗的犬中有15%观察到肾脏病变,对照组为65%。根据这些标准,该疫苗能够显著预防接种疫苗动物中的钩端螺旋体病(P=0.0001)。本研究确定了四价疫苗中流感伤寒型血清型部分预防疾病和肾脏排泄钩端螺旋体的免疫持续时间至少为15个月。

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