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异源DNA疫苗-减毒活疫苗初免-加强免疫对高致病性猪繁殖与呼吸综合征病毒感染的阳性免疫调节作用。

Positive immunomodulatory effects of heterologous DNA vaccine- modified live vaccine, prime-boost immunization, against the highly-pathogenic PRRSV infection.

作者信息

Sirisereewan Chaitawat, Nedumpun Teerawut, Kesdangsakonwut Sawang, Woonwong Yonlayong, Kedkovid Roongtham, Arunorat Jirapat, Thanawongnuwech Roongroje, Suradhat Sanipa

机构信息

Graduate Program in Veterinary Pathobiology, Faculty of Veterinary Science, Chulalongkorn University, Pathumwan, Bangkok 10330, Thailand.

Interdisciplinary Program in Medical Microbiology, Graduate School, Chulalongkorn University, Pathumwan, Bangkok 10330, Thailand.

出版信息

Vet Immunol Immunopathol. 2017 Jan;183:7-15. doi: 10.1016/j.vetimm.2016.11.002. Epub 2016 Nov 11.

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) infection is one of the most important swine pathogens, and causes a major economic impact worldwide. Recently, a new variant type 2 PRRSV, highly pathogenic PRRSV (HP-PRRSV) has emerged and continued to circulate in Southeast Asia region. Currently, commercially available PRRSV vaccines, modified live PRRS vaccines (MLV) are not able to provide complete protection against HP-PRRSV and been reported to induce negative immunomodulatory effects. Interestingly, a novel DNA vaccine was developed and successfully used to improve PRRSV-specific immune responses following MLV vaccination. To investigate the efficacy of a heterologous DNA-MLV prime-boost immunization against the HP-PRRSV infection, an experimental vaccinated-challenged study was conducted. Two-week-old, PRRSV-seronegative, crossbred pigs (5-8 pigs/group) were allocated into 5 groups. At day -14 (D-14), the treatment group (DNA-MLV) was immunized with a DNA vaccine encoding PRRSV-truncated nucleocapsid protein (pORF7t), followed by a commercial modified live type 2 PRRS vaccine (MLV) at D0. The other groups included the group that received PBS at D-14 followed by MLV at D0 (MLV), pORF7t at D-14 (DNA), PBS at D0 (PBS) and the negative control group. At D42, all groups, except the negative control group, were challenged with HP-PRRSV (strain 10PL1). The results demonstrated that pigs that received MLV, regardless of the DNA priming, exhibited less clinical signs and faster viral clearance. Following HP-PRRSV challenge, the DNA-MLV group exhibited improved PRRSV-specific immunity, as observed by increased neutralizing antibody titers and PRRSV-specific IFN-γ production, and reduced IL-10 and PRRSV-specific Treg productions. However, neither the prime-boost immunization nor the MLV was able to induce complete clinical protection against HP-PRRSV infection. In conclusion, improved immunological responses, but not clinical protection, were achieved by DNA-MLV prime-boost immunization. This study highlights the potential use of heterologous prime-boost vaccination regimen, where DNA can be incorporated with other vaccine candidates, for improving anti-PRRSV immunity that may eventually lead induction of complete PRRSV protection.

摘要

猪繁殖与呼吸综合征病毒(PRRSV)感染是最重要的猪病原体之一,在全球范围内造成重大经济影响。最近,一种新的2型变异PRRSV,即高致病性PRRSV(HP-PRRSV)出现并继续在东南亚地区传播。目前,市售的PRRSV疫苗,即改良活PRRS疫苗(MLV),无法提供针对HP-PRRSV的完全保护,并且据报道会诱导负面的免疫调节作用。有趣的是,一种新型DNA疫苗被开发出来,并成功用于改善MLV疫苗接种后的PRRSV特异性免疫反应。为了研究异源DNA-MLV初免-加强免疫对HP-PRRSV感染的效果,进行了一项实验性疫苗接种-攻毒研究。将两周龄、PRRSV血清阴性的杂交猪(每组5-8头)分为5组。在第-14天(D-14),治疗组(DNA-MLV)用编码PRRSV截短核衣壳蛋白的DNA疫苗(pORF7t)免疫,然后在D0用市售改良活2型PRRS疫苗(MLV)免疫。其他组包括在D-14接受PBS然后在D0接受MLV的组(MLV)、在D-14接受pORF7t的组(DNA)、在D0接受PBS的组(PBS)和阴性对照组。在D42,除阴性对照组外,所有组都用HP-PRRSV(10PL1株)攻毒。结果表明,接受MLV的猪,无论是否进行DNA初免,临床症状都较轻,病毒清除速度更快。在HP-PRRSV攻毒后,DNA-MLV组表现出改善的PRRSV特异性免疫,表现为中和抗体滴度增加和PRRSV特异性IFN-γ产生增加,以及IL-10和PRRSV特异性Treg产生减少。然而,初免-加强免疫和MLV都不能诱导对HP-PRRSV感染的完全临床保护。总之,DNA-MLV初免-加强免疫实现了免疫反应的改善,但没有实现临床保护。这项研究突出了异源初免-加强疫苗接种方案的潜在用途,其中DNA可以与其他候选疫苗结合使用,以改善抗PRRSV免疫,最终可能导致诱导完全的PRRSV保护。

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