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南京医科大学学报(自然科学版)                                  第46卷第7期
               ·1020 ·                    Journal of Nanjing Medical University(Natural Sciences)   2026年7月


             ·基础研究·

              流感病毒裂解疫苗佐剂对比:Alum⁃CpG 肌肉注射与糖纳米颗

              粒鼻喷递送的免疫保护效果评价



              李永琪 ,蒋正东 ,张玮欣 ,季旻珺 ,王桂芹                     2*
                                       1,2
                                                 1*
                     1,2
                               3
               南京医科大学国家疫苗研发创新平台,国家卫生健康委抗体技术重点实验室,病原感染与防治研究省高校重点实验室,南京
              1
              医科大学基础医学院病原生物学系,江苏                南京   211166;中科南京生命健康高等研究院,江苏               南京   211135;深圳康泰
                                                                                                       3
                                                            2
              生物制品股份有限公司,广东 深圳              518107
             [摘    要] 目的:基于同一裂解疫苗抗原体系,比较铝佐剂⁃寡核苷酸(aluminum adjuvant⁃CpG oligodeoxynucleotide,Alum⁃CpG)
              复合佐剂肌肉注射与糖纳米颗粒(sugar⁃based lipid nanoparticle,SNP)鼻喷递送两种免疫策略的保护效果。方法:将 8 周龄
              BALB/c 雌性小鼠随机分为Alum⁃CpG组、SNP组、仅肌注裂解疫苗的Split vaccine组及未免疫的对照组,共免疫2次,间隔14 d。
              加强免疫后第14天采集血清及鼻腔灌洗液(nasal lavage fluid,NLF),采用血凝抑制(hemagglutination inhibition,HI)试验和间接
              酶联免疫吸附试验检测抗体水平。随后以异源流感病毒 A/Scotland/P2/2015(H1N1)进行攻毒,评价各组小鼠体重变化、存活
              率、肺组织病毒载量及肺部病理学改变。结果:在相同抗原剂量条件下,Alum⁃CpG组显著提高血清HI抗体效价,攻毒后小鼠
              存活率达100%,并显著降低肺组织流感病毒载量、减轻肺部炎性损伤。SNP组虽能诱导一定水平的HI抗体和分泌型免疫球
              蛋白A(secretory immunoglobulin A,sIgA)抗体并提供部分保护,但其HI抗体效价、存活率及病毒清除效果均低于Alum⁃CpG组
              及Split vaccine组,部分小鼠肺组织中仍可检测到较高水平的病毒复制。结论:Alum⁃CpG复合佐剂肌肉注射策略可显著提升
              裂解疫苗的免疫原性与保护效力,免疫增强作用优于SNP鼻喷递送;SNP作为鼻喷载体具有应用潜力,但需进一步优化其自身
              设计以提高保护效果。
             [关键词] 流感病毒;裂解疫苗;铝佐剂;寡脱氧核苷酸;糖纳米颗粒
             [中图分类号] R392.11                  [文献标志码] A                      [文章编号] 1007⁃4368(2026)07⁃1020⁃09
              doi:10.7655/NYDXBNSN260133


              Adjuvant comparison for influenza virus split vaccine:evaluation of immune protective

              efficacy between Alum⁃CpG and sugar⁃based lipid nanoparticles
                                                                  1*
                                                       1,2
                                        3
                      1,2
              LI Yongqi ,JIANG Zhengdong ,ZHANG Weixin ,JI Minjun ,WANG Guiqin  2*
              1 National Innovation Platform for the Integration of Industry and Education in Vaccine;NHC Key Laboratory of
              Antibody Technique; Provincial Key Laboratory for Pathogen Infection and Prevention Research,Department of
              Pathogenic Biology,School of Basic Medical Sciences,Nanjing Medical University,Nanjing 211166;Nanjing
                                                                                                       2
              Institute of Life and Health Sciences,China University of Science and Technology,Nanjing 211135;Shenzhen
                                                                                                      3
              Kangtai Biological Products Co.,Ltd.,Shenzhen 518107,China

             [Abstract] Objective:This study focused on the same split vaccine antigen system to compare the protective efficacy of two
              immunization strategies:intramuscular injection with aluminum adjuvant ⁃ CpG oligodeoxynucleotide(Alum ⁃ CpG)and intranasal
              delivery with sugar⁃based lipid nanoparticles(SNP). Methods:Eight⁃week⁃old female BALB/c mice were randomly assigned into
              different experimental groups:Alum⁃CpG group,SNP group,intramuscular unadjuvanted split vaccine group,and unimmunized control
              group. All mice received two immunizations 14 days apart. On day 14 after the booster immunization,serum and nasal lavage fluid(NLF)
              were collected. Antibody levels were measured by hemagglutination inhibition(HI)assay and indirect enzyme⁃linked immunosorbent

             [基金项目] 江苏省科技厅社会发展项目(BE2021756);江苏省“双创人才”项目(JSSCRC2023555)
               通信作者(Corresponding author),E⁃mail:Jiminjun@njmu.edu.cn(ORCID:0000⁃0003⁃0293⁃0255);Gqwang@ipsnanjing.cn(ORCID:
              ∗
              0000⁃0002⁃5733⁃1797)
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