Weingartl Hana M, Berhane Yohannes, Caswell Jeff L, Loosmore Sheena, Audonnet Jean-Christophe, Roth James A, Czub Markus
NCFAD, CFIA, 1015 Arlington St., Winnipeg, Manitoba R3E 3M4, Canada.
J Virol. 2006 Aug;80(16):7929-38. doi: 10.1128/JVI.00263-06.
Nipah virus (NiV), of the family Paramyxoviridae, was isolated in 1999 in Malaysia from a human fatality in an outbreak of severe human encephalitis, when human infections were linked to transmission of the virus from pigs. Consequently, a swine vaccine able to abolish virus shedding is of veterinary and human health interest. Canarypox virus-based vaccine vectors carrying the gene for NiV glycoprotein (ALVAC-G) or the fusion protein (ALVAC-F) were used to intramuscularly immunize four pigs per group, either with 10(8) PFU each or in combination. Pigs were boosted 14 days postvaccination and challenged with 2.5 x 10(5) PFU of NiV two weeks later. The combined ALVAC-F/G vaccine induced the highest levels of neutralization antibodies (2,560); despite the low neutralizing antibody levels in the F vaccinees (160), all vaccinated animals appeared to be protected against challenge. Virus was not isolated from the tissues of any of the vaccinated pigs postchallenge, and a real-time reverse transcription (RT)-PCR assay detected only small amounts of viral RNA in several samples. In challenge control pigs, virus was isolated from a number of tissues (10(4.4) PFU/g) or detected by real-time RT-PCR. Vaccination of the ALVAC-F/G vaccinees appeared to stimulate both type 1 and type 2 cytokine responses. Histopathological findings indicated that there was no enhancement of lesions in the vaccinees. No virus shedding was detected in vaccinated animals, in contrast to challenge control pigs, from which virus was isolated from the throat and nose (10(2.9) PFU/ml). Based on the data presented, the combined ALVAC-F/G vaccine appears to be a very promising vaccine candidate for swine.
尼帕病毒(NiV)属于副粘病毒科,1999年在马来西亚从一名死于严重人类脑炎疫情的患者身上分离出来,当时人类感染与该病毒从猪的传播有关。因此,一种能够消除病毒 shedding 的猪用疫苗对兽医和人类健康都具有重要意义。携带尼帕病毒糖蛋白基因(ALVAC-G)或融合蛋白基因(ALVAC-F)的基于金丝雀痘病毒的疫苗载体,以每组四只猪进行肌肉注射免疫,每只猪注射10⁸ PFU或两种组合使用。猪在接种疫苗后14天进行加强免疫,两周后用2.5×10⁵ PFU的尼帕病毒进行攻毒。联合ALVAC-F/G疫苗诱导产生了最高水平的中和抗体(2560);尽管F疫苗接种组的中和抗体水平较低(160),但所有接种疫苗的动物似乎都受到了保护,免受攻毒。攻毒后,未从任何接种疫苗的猪的组织中分离到病毒,实时逆转录(RT)-PCR检测仅在几个样本中检测到少量病毒RNA。在攻毒对照猪中,从多个组织中分离到病毒(10⁴.⁴ PFU/g)或通过实时RT-PCR检测到病毒。接种ALVAC-F/G疫苗的猪似乎刺激了1型和2型细胞因子反应。组织病理学结果表明,接种疫苗的猪的病变没有加重。与攻毒对照猪不同,接种疫苗的动物未检测到病毒 shedding,攻毒对照猪的喉咙和鼻子中分离到病毒(10².⁹ PFU/ml)。根据所提供的数据,联合ALVAC-F/G疫苗似乎是一种非常有前途的猪用疫苗候选物。