Moon Sung-Sil, Richter-Roche Marly, Resch Theresa K, Wang Yuhuan, Foytich Kimberly R, Wang Houping, Mainou Bernardo A, Pewin Winston, Lee Jeongwoo, Henry Sebastien, McAllister Devin V, Jiang Baoming
Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Micron Biomedical, Inc., Atlanta, GA, USA.
NPJ Vaccines. 2022 Feb 28;7(1):26. doi: 10.1038/s41541-022-00443-7.
We recently reported a lack of interference between inactivated rotavirus vaccine (IRV) and inactivated poliovirus vaccine (IPV) and their potential dose sparing when the two vaccines were administered intramuscularly either in combination or standalone in rats and guinea pigs. In the present study, we optimized the formulations of both vaccines and investigated the feasibility of manufacturing a combined IRV-IPV dissolving microneedle patch (dMNP), assessing its compatibility and immunogenicity in rats. Our results showed that IRV delivered by dMNP alone or in combination with IPV induced similar levels of RV-specific IgG and neutralizing antibody. Likewise, IPV delivered by dMNP alone or in combination with IRV induced comparable levels of neutralizing antibody of poliovirus types 1, 2, and 3. We further demonstrated high stability of IRV-dMNP at 5, 25, and 40 °C and IPV-dMNP at 5 and 25 °C, and found that three doses of IRV or IPV when co-administered at a quarter dose was as potent as a full target dose in inducing neutralizing antibodies against corresponding rotavirus or poliovirus. We conclude that IRV-IPV dMNP did not interfere with each other in triggering an immunologic response and were highly immunogenic in rats. Our findings support the further development of this innovative approach to deliver a novel combination vaccine against rotavirus and poliovirus in children throughout the world.
我们最近报道,在大鼠和豚鼠中,将灭活轮状病毒疫苗(IRV)和灭活脊髓灰质炎病毒疫苗(IPV)联合或单独肌内注射时,二者之间不存在干扰,且具有潜在的剂量节省效应。在本研究中,我们优化了两种疫苗的配方,并研究了制备IRV-IPV联合溶解微针贴片(dMNP)的可行性,评估了其在大鼠中的相容性和免疫原性。我们的结果表明,单独使用dMNP或与IPV联合使用时,IRV诱导的RV特异性IgG和中和抗体水平相似。同样,单独使用dMNP或与IRV联合使用时,IPV诱导的1型、2型和3型脊髓灰质炎病毒中和抗体水平相当。我们进一步证明了IRV-dMNP在5、25和40°C下以及IPV-dMNP在5和25°C下具有高稳定性,并且发现三剂IRV或IPV以四分之一剂量共同给药时,在诱导针对相应轮状病毒或脊髓灰质炎病毒的中和抗体方面与全靶剂量一样有效。我们得出结论,IRV-IPV dMNP在触发免疫反应时不会相互干扰,并且在大鼠中具有高度免疫原性。我们的研究结果支持进一步开发这种创新方法,以在全球儿童中提供一种新型的抗轮状病毒和脊髓灰质炎病毒联合疫苗。