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黏膜免疫应答在鼻腔相关淋巴组织中的作用:佐剂经鼻腔给药后的效果

Mucosal Immune Response in Nasal-Associated Lymphoid Tissue upon Intranasal Administration by Adjuvants.

机构信息

Department of Vaccine Immunology, Graduate School of Medicine, Hokkaido University, Sapporo,

Department of Human Immunology, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Sapporo,

出版信息

J Innate Immun. 2018;10(5-6):515-521. doi: 10.1159/000489405. Epub 2018 Jun 1.


DOI:10.1159/000489405
PMID:29860261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6784108/
Abstract

The nasal administration of vaccines directed against diseases caused by upper respiratory tract infections of pathogens, such as the influenza virus, mimics the natural infection of pathogens and induces immunoglobulin A (IgA) production in the nasal cavity to effectively protect viral entry. Therefore, the development of a nasally administered vaccine is a research objective. Because the antigenicity of influenza split vaccines is low, nasal inoculation with the vaccine alone does not induce strong IgA production in the nasal cavity. However, the addition of adjuvants activates the innate immune response, enhancing antigen-specific IgA production and the T-cell response. Although the development of suitable adjuvants for nasal vaccinations is in progress, the mechanism by which adjuvants promote the immune response is still unclear. In this review, we discuss the mucosal immune response, especially in the nasal-associated lymphoid tissue, induced in response to the intranasal inoculation of an influenza vaccine and adjuvants in animal models.

摘要

鼻腔给药的疫苗针对的是由病原体引起的上呼吸道感染疾病,如流感病毒,模拟了病原体的自然感染,并在鼻腔中诱导产生免疫球蛋白 A(IgA),从而有效地保护病毒进入。因此,开发鼻腔给药的疫苗是一个研究目标。由于流感裂解疫苗的抗原性低,单独鼻腔接种疫苗不会在鼻腔中诱导强烈的 IgA 产生。但是,佐剂的添加激活了先天免疫反应,增强了抗原特异性 IgA 产生和 T 细胞反应。尽管正在开发适合鼻腔接种的佐剂,但佐剂促进免疫反应的机制仍不清楚。在这篇综述中,我们讨论了在动物模型中,针对流感疫苗和佐剂鼻腔接种所引起的黏膜免疫反应,特别是在鼻相关淋巴组织中的免疫反应。

相似文献

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Mucosal Immune Response in Nasal-Associated Lymphoid Tissue upon Intranasal Administration by Adjuvants.

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本文引用的文献

[1]
cGAMP Promotes Germinal Center Formation and Production of IgA in Nasal-Associated Lymphoid Tissue.

Med Sci (Basel). 2017-12-18

[2]
Toll-like receptor 3 in nasal CD103 dendritic cells is involved in immunoglobulin A production.

Mucosal Immunol. 2017-6-15

[3]
Intranasal Inactivated Influenza Vaccines: a Reasonable Approach to Improve the Efficacy of Influenza Vaccine?

Jpn J Infect Dis. 2016

[4]
Exploiting Mucosal Immunity for Antiviral Vaccines.

Annu Rev Immunol. 2016-5-20

[5]
Differences in the paranasal sinuses between germ-free and pathogen-free mice.

Int Forum Allergy Rhinol. 2016-6

[6]
Microbiota regulate the ability of lung dendritic cells to induce IgA class-switch recombination and generate protective gastrointestinal immune responses.

J Exp Med. 2016-1-11

[7]
RANKL regulates differentiation of microfold cells in mouse nasopharynx-associated lymphoid tissue (NALT).

Cell Tissue Res. 2016-4

[8]
The mucosal adjuvant cyclic di-GMP enhances antigen uptake and selectively activates pinocytosis-efficient cells in vivo.

Elife. 2015-4-21

[9]
Influenza vaccines: challenges and solutions.

Cell Host Microbe. 2015-3-11

[10]
Defined TLR3-specific adjuvant that induces NK and CTL activation without significant cytokine production in vivo.

Nat Commun. 2015-2-18

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