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在公羊中使用聚合抗原BLSOmp31进行短期免疫接种引发的针对绵羊布鲁氏菌的免疫反应和血清杀菌活性。

Immune response and serum bactericidal activity against Brucella ovis elicited using a short immunization schedule with the polymeric antigen BLSOmp31 in rams.

作者信息

Díaz Alejandra G, Clausse María, Paolicchi Fernando A, Fiorentino María A, Ghersi Giselle, Zylberman Vanesa, Goldbaum Fernando A, Estein Silvia M

机构信息

Laboratorio de Inmunología, Depto. SAMP, Centro de Investigación Veterinaria de Tandil (CIVETAN)- CONICET, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires (U.N.C.P.B.A.), Tandil, Buenos Aires, Argentina.

出版信息

Vet Immunol Immunopathol. 2013 Jul 15;154(1-2):36-41. doi: 10.1016/j.vetimm.2013.04.003. Epub 2013 Apr 11.

Abstract

Brucella ovis is the etiologic agent of ovine brucellosis. The control measures for this disease are periodical diagnosis by serological tests and/or bacteriological culture and culling of positive animals. Vaccination with Brucella melitensis Rev 1 is recommended when prevalence is high. This attenuated strain vaccine gives protection against B. ovis but it has important disadvantages associated with the development of antibodies interfering with serodiagnosis, virulence for humans and the prohibition of its use in countries considered free of B. melitensis. Consequently, there is a need for new safe and effective brucellosis vaccines to be developed. We have previously reported that the polymeric subcellular vaccine BLSOmp31 confers protection against experimental challenge with B. ovis when rams are immunized three times. In the present work we evaluated and characterized, along 56 weeks after the first immunization of adult rams, the evolution of the immune response elicited by BLSOmp31 using a short immunization schedule.

摘要

绵羊布鲁氏菌是绵羊布鲁氏菌病的病原体。该疾病的控制措施是通过血清学检测和/或细菌学培养进行定期诊断,并扑杀阳性动物。当患病率较高时,建议使用马尔他布鲁氏菌Rev 1疫苗进行接种。这种减毒株疫苗可提供针对绵羊布鲁氏菌的保护,但它具有一些重要缺点,包括会产生干扰血清学诊断的抗体、对人类具有毒力以及在被认为无马尔他布鲁氏菌的国家禁止使用。因此,需要开发新的安全有效的布鲁氏菌病疫苗。我们之前曾报道,当公羊免疫三次时,聚合亚细胞疫苗BLSOmp31可提供针对绵羊布鲁氏菌实验性攻击的保护。在本研究中,我们在成年公羊首次免疫后的56周内,使用短免疫程序评估并表征了BLSOmp31引发的免疫反应的演变。

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