Division of Viral Diseases, Centers for Diseases Control and Prevention, Atlanta, GA, United States.
Serum Institute of India Pvt. Ltd., Pune, India.
Vaccine. 2019 Jan 29;37(5):698-704. doi: 10.1016/j.vaccine.2018.12.043. Epub 2019 Jan 6.
A parenteral inactivated rotavirus vaccine (IRV) in development could address three problems with current live oral rotavirus vaccines (ORV): their lower efficacy in low and middle-income countries (LMICs), lingering concerns about their association with intussusception, and their requirement for a separate supply chain with large volume cold storage. Adding a new parenteral IRV to the current schedule of childhood immunizations would be more acceptable if it could be combined with another injectable vaccine such as inactivated polio vaccine (IPV). Current plans for polio eradication call for phasing out oral polio vaccine (OPV) and transitioning to IPV, initially in LMICs as a single dose booster after two doses of OPV and ultimately as a two dose schedule. Today in many LMICs, IPV is administered as a standalone vaccine, which involves a separate cold chain and is relatively costly. We therefore tested in two animal models formulations of IPV with IRV to determine whether co-administration might interfere with the immune response to each product and spare antigen dose for both vaccines. Our results demonstrate that IRV when adjuvanted with alum and administered alone or in combination with IPV did not impair the immune responses to either rotavirus or poliovirus serotypes 1, 2 and 3. Similarly, IPV when formulated and administered alone or together with IRV induced comparable levels of neutralizing antibody to poliovirus type 1, 2 and 3. Furthermore, comparable antibody titers were observed in animals vaccinated with low, middle or high dose of IPV or IRV in combination. This dose sparing and the lack of interference between IPV and IRV administered together represent another step to support the further development of this novel combination vaccine for children.
一种正在开发的肠道外灭活轮状病毒疫苗(IRV)可以解决目前口服活轮状病毒疫苗(ORV)的三个问题:在中低收入国家(LMIC)的效力较低、对其与肠套叠相关的挥之不去的担忧,以及它们需要单独的冷链和大容量冷藏储存。如果可以将新的肠道外 IRV 与另一种可注射疫苗(如灭活脊髓灰质炎疫苗 [IPV])结合使用,那么将其添加到当前儿童免疫计划中会更容易被接受。当前的根除脊髓灰质炎计划要求逐步淘汰口服脊髓灰质炎疫苗(OPV)并过渡到 IPV,最初在 LMIC 中,OPV 两剂后作为单剂量加强针,最终作为两剂方案。如今,在许多 LMIC 中,IPV 作为单独的疫苗接种,涉及单独的冷链,而且相对昂贵。因此,我们在两种动物模型中测试了 IPV 与 IRV 的配方,以确定联合给药是否会干扰每种产品的免疫反应并节省两种疫苗的抗原剂量。我们的研究结果表明,当与明矾佐剂一起单独给药或与 IPV 联合给药时,IRV 不会损害对轮状病毒或脊髓灰质炎病毒血清型 1、2 和 3 的免疫反应。同样,单独配制和给药的 IPV 或与 IRV 一起诱导的针对脊髓灰质炎病毒 1、2 和 3 的中和抗体水平相当。此外,在接种低、中或高剂量 IPV 或 IRV 组合的动物中观察到相当的抗体滴度。这种剂量节省和联合使用的 IPV 和 IRV 之间没有干扰代表了支持进一步开发这种新型儿童组合疫苗的又一步。