Zhu Feng, Sun Meng-Xu, Zhao Suo-Qun, Qin Cheng-Feng, Wang Jin-Hua, Deng Yong-Qiang
School of Life Sciences, Southwest Forestry University, Kunming 650224, China.
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing 100071, China.
Vaccines (Basel). 2024 Jul 30;12(8):856. doi: 10.3390/vaccines12080856.
Yellow fever (YF), caused by the yellow fever virus (YFV), continually spreads and causes epidemics worldwide, posing a great threat to human health. The live-attenuated YF 17D vaccine (YF-17D) has been licensed for preventing YFV infection and administrated via the intramuscular (i.m.) route. In this study, we sought to determine the immunogenicity and protective efficacy of aerosolized YF-17D via the intratracheal (i.t.) route in mice. YF-17D stocks in liquids were successfully aerosolized into particles of 6 μm. Further in vitro phenotype results showed the aerosolization process did not abolish the infectivity of YF-17D. Meanwhile, a single i.t. immunization with aerosolized YF-17D induced robust humoral and cellular immune responses in A129 mice, which is comparable to that received i.p. immunization. Notably, the aerosolized YF-17D also triggered specific secretory IgA (SIgA) production in bronchoalveolar lavage. Additionally, all immunized animals survived a lethal dose of YFV challenge in mice. In conclusion, our results support further development of aerosolized YF-17D in the future.
黄热病(YF)由黄热病毒(YFV)引起,在全球持续传播并引发疫情,对人类健康构成巨大威胁。减毒活疫苗YF 17D(YF-17D)已获许可用于预防YFV感染,通过肌肉注射(i.m.)途径给药。在本研究中,我们试图确定经气管内(i.t.)途径雾化YF-17D在小鼠中的免疫原性和保护效果。液体中的YF-17D储备液成功雾化成6μm的颗粒。进一步的体外表型结果表明,雾化过程并未消除YF-17D的感染性。同时,单次经气管内免疫雾化YF-17D可在A129小鼠中诱导强烈的体液和细胞免疫反应,这与腹腔内免疫相当。值得注意的是,雾化YF-17D还可在支气管肺泡灌洗中引发特异性分泌型IgA(SIgA)的产生。此外,所有免疫动物在小鼠中均能在致死剂量的YFV攻击下存活。总之,我们的结果支持未来进一步开发雾化YF-17D。