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评价一种新型减毒活皮疙瘩病疫苗在印度的安全性、免疫原性和有效性。

Evaluation of the safety, immunogenicity and efficacy of a new live-attenuated lumpy skin disease vaccine in India.

机构信息

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Indian Veterinary Research Institute, Mukteswar, India.

出版信息

Virulence. 2023 Dec;14(1):2190647. doi: 10.1080/21505594.2023.2190647.

Abstract

Lumpy skin disease (LSD) was reported for the first time in India in 2019 and since then, it has become endemic. Since a homologous (LSD-virus based) vaccine was not available in the country, goatpox virus (GPV)-based heterologous vaccine was authorized for mass immunization to induce protection against LSD in cattle. This study describes the evaluation of safety, immunogenicity and efficacy of a new live-attenuated LSD vaccine developed by using an Indian field strain, isolated in 2019 from cattle. The virus was attenuated by continuous passage ( = 50) in Vero cells. The vaccine (50 LSDV passage in Vero cells, named as Lumpi-ProVac) did not induce any local or systemic reaction upon its experimental inoculation in calves ( = 10). At day 30 post-vaccination (pv), the vaccinated animals were shown to develop antibody- and cell-mediated immune responses and exhibited complete protection upon virulent LSDV challenge. A minimum Neethling response (0.018% animals; 5 out of 26,940 animals) of the vaccine was observed in the field trials conducted in 26,940 animals. There was no significant reduction in the milk yield in lactating animals ( = 10108), besides there was no abortion or any other reproductive disorder in the pregnant animals ( = 2889). Sero-conversion was observed in 85.18% animals in the field by day 30 pv.

摘要

2019 年,印度首次报告了块状皮肤病(LSD),此后该病已成为地方性疾病。由于该国没有同源(基于 LSD 病毒)疫苗,因此授权使用山羊痘病毒(GPV)基于异源疫苗对牛进行大规模免疫接种,以诱导对 LSD 的保护。本研究描述了一种新的减毒 LSD 疫苗的安全性、免疫原性和效力评估,该疫苗是使用 2019 年从牛中分离的印度田间分离株通过连续传代( = 50)在 Vero 细胞中开发的。该疫苗(在 Vero 细胞中连续传代 50 代的 LSDV,命名为 Lumpi-ProVac)在小牛( = 10)的实验接种中未引起任何局部或全身反应。在接种疫苗后 30 天(pv),接种疫苗的动物表现出抗体和细胞介导的免疫反应,并在接种强毒 LSDV 后完全受到保护。在对 26940 只动物进行的现场试验中,观察到疫苗的最小 Neethling 反应(0.018%的动物;26940 只动物中有 5 只)。在哺乳期动物( = 10108)中,产奶量没有明显减少,在妊娠动物( = 2889)中也没有流产或任何其他生殖障碍。在 pv 第 30 天,通过现场观察到 85.18%的动物发生血清转化率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/883b/10038050/a479567e2520/KVIR_A_2190647_F0001_OC.jpg

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