Piazza F M, Johnson S A, Darnell M E, Porter D D, Hemming V G, Prince G A
Children's National Medical Center, Washington, D.C.
J Virol. 1993 Mar;67(3):1503-10. doi: 10.1128/JVI.67.3.1503-1510.1993.
Human respiratory syncytial virus (HRSV) is the most frequent cause of severe respiratory infections in infancy. No vaccine against this virus has yet been protective, and antiviral drugs have been of limited utility. Using the cotton rat model of HRSV infection, we examined bovine respiratory syncytial virus (BRSV), a cause of acute respiratory disease in young cattle, as a possible vaccine candidate to protect children against HRSV infection. Cotton rats were primed intranasally with graded doses of BRSV/375 or HRSV/Long or were left unprimed. Three weeks later, they were challenged intranasally with either BRSV/375, HRSV/Long (subgroup A), or HRSV/18537 (subgroup B). At intervals postchallenge, animals were sacrificed for virus titration and histologic evaluation. Serum neutralizing antibody titers were determined at the time of viral challenge. BRSV/375 replicated to low titers in nasal tissues and lungs. Priming with 10(5) PFU of BRSV/375 effected a 500- to 1,000-fold reduction in peak nasal HRSV titer and a greater than 1,000-fold reduction in peak pulmonary HRSV titer upon challenge with HRSV/Long or HRSV/18537. In contrast to priming with HRSV, priming with BRSV did not induce substantial levels of neutralizing antibody against HRSV and was associated with a delayed onset of clearance of HRSV upon challenge. Priming with BRSV/375 caused mild nasal and pulmonary pathology and did not cause exacerbation of disease upon challenge with HRSV/Long. Our findings suggest that BRSV may be a potential vaccine against HRSV and a useful tool for studying the mechanisms of immunity to HRSV.
人呼吸道合胞病毒(HRSV)是婴儿期严重呼吸道感染最常见的病因。目前尚无针对该病毒的疫苗具有保护作用,抗病毒药物的效用也有限。我们利用HRSV感染的棉鼠模型,研究了牛呼吸道合胞病毒(BRSV),它是幼牛急性呼吸道疾病的病因之一,作为一种可能的候选疫苗来保护儿童免受HRSV感染。用不同剂量的BRSV/375或HRSV/Long经鼻给棉鼠进行初免,或不进行初免。三周后,用BRSV/375、HRSV/Long(A亚组)或HRSV/18537(B亚组)经鼻对它们进行攻击。在攻击后的不同时间间隔,处死动物进行病毒滴定和组织学评估。在病毒攻击时测定血清中和抗体滴度。BRSV/375在鼻组织和肺中复制至低滴度。用10(5) PFU的BRSV/375进行初免,在用HRSV/Long或HRSV/18537攻击后,鼻内HRSV峰值滴度降低500至1000倍,肺内HRSV峰值滴度降低超过1000倍。与用HRSV进行初免不同,用BRSV进行初免不会诱导产生大量针对HRSV的中和抗体,并且与攻击后HRSV清除延迟有关。用BRSV/375进行初免会引起轻微的鼻和肺病理变化,在用HRSV/Long攻击时不会导致疾病加重。我们的研究结果表明,BRSV可能是一种针对HRSV的潜在疫苗,也是研究HRSV免疫机制的有用工具。