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慢性缺氧对疫苗佐剂诱导特异性免疫应答的调控:QML维持稳定而CpG显著增强

张苗苗 李海波 赵心瑶 朱吉 王亚兰 白钰伦 邓炎 江悦 余文康 那顺布和

陆军军医大学学报2026,Vol.48Issue(8):980-990,11.
陆军军医大学学报2026,Vol.48Issue(8):980-990,11.DOI:10.16016/j.2097-0927.202512119

慢性缺氧对疫苗佐剂诱导特异性免疫应答的调控:QML维持稳定而CpG显著增强

Chronic hypoxia modulates vaccine adjuvant-induced specific immune responses:QML maintains stability while CpG significantly enhances

张苗苗 1李海波 2赵心瑶 3朱吉 2王亚兰 2白钰伦 2邓炎 2江悦 2余文康 2那顺布和4

作者信息

  • 1. 内蒙古大学生命科学学院,内蒙古呼和浩特||陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心,重庆
  • 2. 陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心,重庆
  • 3. 陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心,重庆||成都医学院生物科学与技术学院,四川成都
  • 4. 内蒙古大学生命科学学院,内蒙古呼和浩特
  • 折叠

摘要

Abstract

Objective High-altitude chronic hypoxia can alter the immune status,yet the immune regulatory characteristics of various vaccine adjuvants in this environment remain to be fully elucidated.Accordingly,emphasis is placed on evaluating the regulatory effects of chronic hypoxia on specific humoral,cellular,and memory T cell responses elicited by different adjuvants.Methods Using ovalbumin(OVA)as the antigen,Th2-biased adjuvant aluminum hydroxide(Alum),Th1-biased adjuvant CpG,and Th1/Th2-balanced adjuvant QML were combined for intramuscular immunization in mice on days 0 and 14.Th1-biased adjuvant CpG,or Th1/Th2-balanced adjuvant QML for intramuscular immunization on day 0 and 14(n=16).A total of 160 SPF female C57BL/6 mice(6 to 8 weeks old,weighing 16 to 18 g)were randomly divided into 5 groups(n=32):PBS group(sterile PBS),OVA group(5 μg OVA),OVA+Alum group(5 μg OVA and 100 μg Alum),OVA+CpG group(5 μg OVA and 20 μg CpG),and OVA+QML group(5 μg OVA and 50 μL QML).Each group was further divided into normoxia control(n=16,housed in 21%O ₂ environment)and chronic hypoxia(n=16,simulated altitude 5 800 m)subgroups.On days 14 and 60 after the last immunization,the serum levels of specific IgG,IgG1,and IgG2c antibodies were measured by ELISA;enzyme-linked immunospot assay(ELISpot)was used to detect the numbers of cells secreting IFN-γ,IL-4,and IL-17A in the splenocytes.On day 14 after the last immunization,flow cytometry was performed to determine the proportions of CD4 ⁺ IFN-γ ⁺,CD4 ⁺ IL-4 ⁺,CD4 ⁺ IL-17A ⁺,CD8 ⁺ IFN-γ ⁺,and CD8 ⁺ IL-2 ⁺ cell subsets in the spleen.Results Chronic hypoxia significantly inhibited the ability of OVA alone to induce IgG antibodies(P<0.01),and all 3 adjuvants reversed this effect.QML exerted a stable and superior enhancing effect on serum-specific IgG,IgG1,and IgG2c levels compared to CpG(P<0.05).Notably,CpG induced significantly higher levels of total IgG(P<0.01)and IgG1(P<0.05)in the chronic hypoxia group than in the corresponding normoxia group at days 60 after the final immunization.For cellular immunity,QML stably increased the proportions of CD4⁺IFN-γ⁺ and CD4⁺IL-17A⁺ cells,as well as the secretion levels of IFN-γ and IL-4,under both normoxic and hypoxic conditions.In contrast,the T cell regulatory effects of CpG were hypoxia-dependent,with significant enhancement of IFN-γ-secreting cell numbers in the hypoxia group at both short-term(14 d,P<0.01)and long-term(60 d,P<0.05)time points.Analysis of memory T cells showed that all 3 adjuvants maintained CD4⁺Tcm levels under hypoxia.Additionally,CpG increased the proportions of CD8 ⁺ Tcm(P<0.05)and CD8 ⁺ Tem(P<0.01)in the hypoxic group,while Alum only specifically elevated CD4 ⁺ Tem levels under hypoxic conditions(P<0.05).Conclusion QML stably induces comprehensive immune responses under both normoxic and hypoxic conditions,while CpG exhibits advantages in Th1-type response enhancement and CD8⁺memory T cell expansion under chronic hypoxia,providing experimental evidence for adjuvant selection in chronic hypoxic environments such as high-altitude regions.

关键词

慢性缺氧/常氧/疫苗佐剂/体液免疫/细胞免疫

Key words

chronic hypoxia/normoxia/vaccine adjuvants/humoral immunity/cellular immunity

分类

医药卫生

引用本文复制引用

张苗苗,李海波,赵心瑶,朱吉,王亚兰,白钰伦,邓炎,江悦,余文康,那顺布和..慢性缺氧对疫苗佐剂诱导特异性免疫应答的调控:QML维持稳定而CpG显著增强[J].陆军军医大学学报,2026,48(8):980-990,11.

基金项目

国家自然科学基金面上项目(32270988) (32270988)

重庆市自然科学基金面上项目(CSTB2024NSCQ-MSX0981) Supported by the General Program of National Natural Science Foundation of China(32270988)and the General Project of Natural Science Foundation of Chongqing(CSTB2024NSCQ-MSX0981). (CSTB2024NSCQ-MSX0981)

陆军军医大学学报

2097-0927

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