Khurana Surender, Coyle Elizabeth M, Manischewitz Jody, King Lisa R, Gao Jin, Germain Ronald N, Schwartzberg Pamela L, Tsang John S, Golding Hana
1Division of Viral Products, Center for Biologics Evaluation and Research (CBER), FDA, Silver Spring, MD 20993 USA.
2Center for Human Immunology (CHI), NIH, Bethesda, MD 20892 USA.
NPJ Vaccines. 2018 Oct 1;3:40. doi: 10.1038/s41541-018-0076-2. eCollection 2018.
Immune responses to inactivated vaccines against avian influenza are poor due in part to lack of immune memory. Adjuvants significantly increased virus neutralizing titers. We performed comprehensive analyses of polyclonal antibody responses following FDA-approved adjuvanted H5N1-A/Indonesia vaccine, administered in presence or absence of AS03. Using Whole Genome Fragment Phage Display Libraries, we observed that AS03 induced antibody epitope diversity to viral hemagglutinin (HA) and neuraminidase compared with unadjuvanted vaccine. Furthermore, AS03 promoted significant antibody affinity maturation to properly folded H5-HA1 (but not to HA2) domain, which correlated with neutralization titers against both vaccine and heterologous H5N1 strains. However, no increase in heterosubtypic cross-neutralization of Group1-H1N1 seasonal strains was observed. AS03-H5N1 vaccine also induced higher neuraminidase inhibition antibody titers. This study provides insight into the differential impacts of AS03 adjuvant on H5N1 vaccine-induced antibody responses that may help optimize vaccine platforms for future vaccines with improved protection against seasonal and pandemic influenza strains.
针对禽流感的灭活疫苗的免疫反应较差,部分原因是缺乏免疫记忆。佐剂可显著提高病毒中和滴度。我们对美国食品药品监督管理局(FDA)批准的含佐剂H5N1-A/印度尼西亚疫苗在有或无AS03存在的情况下接种后的多克隆抗体反应进行了全面分析。使用全基因组片段噬菌体展示文库,我们观察到与无佐剂疫苗相比,AS03诱导了针对病毒血凝素(HA)和神经氨酸酶的抗体表位多样性。此外,AS03促进了针对正确折叠的H5-HA1(而非HA2)结构域的显著抗体亲和力成熟,这与针对疫苗和异源H5N1毒株的中和滴度相关。然而,未观察到对1组H1N1季节性毒株的异亚型交叉中和作用增加。AS03-H5N1疫苗还诱导了更高的神经氨酸酶抑制抗体滴度。本研究深入了解了AS03佐剂对H5N1疫苗诱导的抗体反应的不同影响,这可能有助于优化疫苗平台,以开发出对季节性和大流行性流感毒株具有更好保护作用的未来疫苗。