• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Mucosal immunity in COVID-19: a comprehensive review.COVID-19 中的黏膜免疫:全面综述。
Front Immunol. 2024 Aug 14;15:1433452. doi: 10.3389/fimmu.2024.1433452. eCollection 2024.
2
Mucosal Immunity in COVID-19: A Neglected but Critical Aspect of SARS-CoV-2 Infection.COVID-19 中的黏膜免疫:被忽视但至关重要的 SARS-CoV-2 感染方面。
Front Immunol. 2020 Nov 30;11:611337. doi: 10.3389/fimmu.2020.611337. eCollection 2020.
3
Mucosal immunity to severe acute respiratory syndrome coronavirus 2 infection.黏膜免疫对严重急性呼吸综合征冠状病毒 2 感染的作用。
Curr Opin Infect Dis. 2021 Jun 1;34(3):181-186. doi: 10.1097/QCO.0000000000000724.
4
An Intranasal OMV-Based Vaccine Induces High Mucosal and Systemic Protecting Immunity Against a SARS-CoV-2 Infection.一种基于鼻腔内的 OMV 疫苗可诱导针对 SARS-CoV-2 感染的高黏膜和全身保护免疫。
Front Immunol. 2021 Dec 17;12:781280. doi: 10.3389/fimmu.2021.781280. eCollection 2021.
5
SARS-CoV-2 convalescence and hybrid immunity elicits mucosal immune responses.SARS-CoV-2 恢复期和混合免疫引发黏膜免疫应答。
EBioMedicine. 2023 Dec;98:104893. doi: 10.1016/j.ebiom.2023.104893. Epub 2023 Nov 29.
6
Intranasal SARS-CoV-2 Omicron variant vaccines elicit humoral and cellular mucosal immunity in female mice.鼻腔内接种 SARS-CoV-2 奥密克戎变异株疫苗可在雌性小鼠中诱导体液和细胞黏膜免疫。
EBioMedicine. 2024 Jul;105:105185. doi: 10.1016/j.ebiom.2024.105185. Epub 2024 Jun 7.
7
Sex-biased immunogenicity of a mucosal subunit vaccine against SARS-CoV-2 in mice.针对 SARS-CoV-2 的黏膜亚单位疫苗在小鼠中的性别偏向性免疫原性。
Front Immunol. 2024 May 21;15:1386243. doi: 10.3389/fimmu.2024.1386243. eCollection 2024.
8
Peritoneal Administration of a Subunit Vaccine Encapsulated in a Nanodelivery System Not Only Augments Systemic Responses against SARS-CoV-2 but Also Stimulates Responses in the Respiratory Tract.纳米递药系统包裹的亚单位疫苗经腹腔给药不仅增强了针对 SARS-CoV-2 的全身反应,还刺激了呼吸道的反应。
Viruses. 2021 Nov 2;13(11):2202. doi: 10.3390/v13112202.
9
COVID-19: to vaccinate or not to vaccinate - that is the question.COVID-19:接种还是不接种疫苗——这是个问题。
Cas Lek Cesk. 2024;163(4):131-136.
10
Frontline workers: Mediators of mucosal immunity in community acquired pneumonia and COVID-19.一线工作者:社区获得性肺炎和 COVID-19 黏膜免疫的介导者。
Front Immunol. 2022 Sep 23;13:983550. doi: 10.3389/fimmu.2022.983550. eCollection 2022.

引用本文的文献

1
Mucosal Vaccination Against SARS-CoV-2 Using Human Probiotic Spores as an Adjuvant Induces Potent Systemic and Mucosal Immunity.使用人类益生菌孢子作为佐剂的针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的黏膜疫苗可诱导强大的全身和黏膜免疫。
Vaccines (Basel). 2025 Jul 21;13(7):772. doi: 10.3390/vaccines13070772.
2
A 22 month prospective assessment of neutralizing and IgG antibody levels against SARS-CoV-2 variants following homologous and heterologous BNT162b2 boosting.同源和异源BNT162b2加强免疫后针对SARS-CoV-2变异株的中和抗体和IgG抗体水平的22个月前瞻性评估。
Sci Rep. 2025 Jul 1;15(1):21175. doi: 10.1038/s41598-025-05377-3.
3
A single-dose intranasal immunization with a novel bat influenza A virus-vectored MERS vaccine provides effective protection against lethal MERS-CoV challenge.用一种新型甲型蝙蝠流感病毒载体中东呼吸综合征疫苗进行单剂量鼻内免疫可有效抵御致死性中东呼吸综合征冠状病毒攻击。
mBio. 2025 Jun 30:e0110725. doi: 10.1128/mbio.01107-25.
4
Microneedle Delivery of Heterologous Microparticulate COVID-19 Vaccine Induces Cross Strain Specific Antibody Levels in Mice.异源微粒新冠疫苗的微针递送可诱导小鼠产生跨毒株特异性抗体水平。
Vaccines (Basel). 2025 Apr 1;13(4):380. doi: 10.3390/vaccines13040380.
5
Glycosylated Receptor-Binding-Domain-Targeting Mucosal Vaccines Protect Against SARS-CoV-2 Omicron and MERS-CoV.靶向糖基化受体结合域的黏膜疫苗可预防新冠病毒奥密克戎变异株和中东呼吸综合征冠状病毒。
Vaccines (Basel). 2025 Mar 10;13(3):293. doi: 10.3390/vaccines13030293.
6
BA.1 breakthrough infection elicits distinct antibody and memory B cell responses in vaccinated-only versus hybrid immunity individuals.BA.1突破性感染在仅接种疫苗者与混合免疫个体中引发不同的抗体和记忆B细胞反应。
iScience. 2025 Feb 5;28(4):111962. doi: 10.1016/j.isci.2025.111962. eCollection 2025 Apr 18.

本文引用的文献

1
Unmasking the potential of secretory IgA and its pivotal role in protection from respiratory viruses.揭示分泌型免疫球蛋白 A 的潜力及其在预防呼吸道病毒感染中的关键作用。
Antiviral Res. 2024 Mar;223:105823. doi: 10.1016/j.antiviral.2024.105823. Epub 2024 Feb 6.
2
The role of cross-reactive immunity to emerging coronaviruses: Implications for novel universal mucosal vaccine design.新兴冠状病毒交叉反应性免疫的作用:对新型通用黏膜疫苗设计的启示。
Saudi Med J. 2023 Oct;44(10):965-972. doi: 10.15537/smj.2023.44.10.20230375.
3
SARS-CoV-2: Immunity, Challenges with Current Vaccines, and a Novel Perspective on Mucosal Vaccines.严重急性呼吸综合征冠状病毒2:免疫、当前疫苗面临的挑战以及黏膜疫苗的新视角
Vaccines (Basel). 2023 Apr 15;11(4):849. doi: 10.3390/vaccines11040849.
4
Current status of mucosal vaccines against SARS-CoV2: a hope for protective immunity.黏膜疫苗对抗 SARS-CoV-2 的现状:对保护性免疫的希望。
Expert Opin Biol Ther. 2023 Feb;23(2):207-222. doi: 10.1080/14712598.2022.2156284. Epub 2023 Jan 11.
5
Mucosal TLR2-activating protein-based vaccination induces potent pulmonary immunity and protection against SARS-CoV-2 in mice.基于黏膜 TLR2 激活蛋白的疫苗接种可诱导小鼠肺部产生强烈的免疫应答并预防 SARS-CoV-2。
Nat Commun. 2022 Nov 15;13(1):6972. doi: 10.1038/s41467-022-34297-3.
6
Considerations for Novel COVID-19 Mucosal Vaccine Development.新型新冠病毒黏膜疫苗研发的考量因素
Vaccines (Basel). 2022 Jul 23;10(8):1173. doi: 10.3390/vaccines10081173.
7
SARS-CoV-2: A Master of Immune Evasion.严重急性呼吸综合征冠状病毒2:免疫逃逸的高手
Biomedicines. 2022 Jun 7;10(6):1339. doi: 10.3390/biomedicines10061339.
8
Escape and Over-Activation of Innate Immune Responses by SARS-CoV-2: Two Faces of a Coin.SARS-CoV-2 引发的固有免疫反应的逃逸和过度激活:一枚硬币的两面。
Viruses. 2022 Mar 4;14(3):530. doi: 10.3390/v14030530.
9
Systemic and Lower Respiratory Tract Immunity to SARS-CoV-2 Omicron and Variants in Pediatric Severe COVID-19 and Mis-C.儿童重症新冠病毒病及新冠病毒感染相关儿童多系统炎症综合征中针对严重急性呼吸综合征冠状病毒2奥密克戎变异株及其他变异株的全身和下呼吸道免疫
Vaccines (Basel). 2022 Feb 10;10(2):270. doi: 10.3390/vaccines10020270.
10
Prolonged activation of nasal immune cell populations and development of tissue-resident SARS-CoV-2-specific CD8 T cell responses following COVID-19.COVID-19 后,鼻免疫细胞群体持续激活,并产生组织驻留的 SARS-CoV-2 特异性 CD8 T 细胞应答。
Nat Immunol. 2022 Jan;23(1):23-32. doi: 10.1038/s41590-021-01095-w. Epub 2021 Dec 22.

COVID-19 中的黏膜免疫:全面综述。

Mucosal immunity in COVID-19: a comprehensive review.

机构信息

Basic Medical Sciences Department, Faculty of Medicine, Taibah University, Medina, Saudi Arabia.

出版信息

Front Immunol. 2024 Aug 14;15:1433452. doi: 10.3389/fimmu.2024.1433452. eCollection 2024.

DOI:10.3389/fimmu.2024.1433452
PMID:39206184
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11349522/
Abstract

Mucosal immunity plays a crucial role in defending against coronaviruses, particularly at respiratory sites, serving as the first line of defense against viral invasion and replication. Coronaviruses have developed various immune evasion strategies at the mucosal immune system, hindering the recognition of infected cells and evading antibody responses. Understanding the immune mechanisms and responses is crucial for developing effective vaccines and therapeutics against coronaviruses. The role of mucosal immunity in COVID-19 is significant, influencing both local and systemic immune responses to the virus. Although most clinical studies focus on antibodies and cellular immunity in peripheral blood, mucosal immune responses in the respiratory tract play a key role in the early restriction of viral replication and the clearance of SARS-CoV-2. Identification of mucosal biomarkers associated with viral clearance will allow monitoring of infection-induced immunity. Mucosally delivered vaccines and those under clinical trials are being compared and contrasted to understand their effectiveness in inducing mucosal immunity against coronaviruses. A greater understanding of lung tissue-based immunity may lead to improved diagnostic and prognostic procedures and novel treatment strategies aimed at reducing the disease burden of community-acquired pneumonia, avoiding the systemic manifestations of infection and excess morbidity and mortality. This comprehensive review article outlines the current evidence about the role of mucosal immune responses in the clearance of SARS-CoV-2 infection, as well as potential mucosal mechanisms of protection against (re-)infection. It also proposes that there is a significant role for mucosal immunity and for secretory as well as circulating IgA antibodies in COVID-19, and that it is important to elucidate this in order to comprehend especially the asymptomatic and mild states of the infection, which appear to account for the majority of cases. Moreover, it is possible that mucosal immunity can be exploited for beneficial diagnostic, therapeutic, or prophylactic purposes. The findings from recent studies on mucosal immunity in COVID-19 can be used to develop effective vaccines and treatments that can effectively target both mucosal and systemic immune responses.

摘要

黏膜免疫在抵御冠状病毒方面起着至关重要的作用,特别是在呼吸道部位,作为抵御病毒入侵和复制的第一道防线。冠状病毒在黏膜免疫系统中发展了多种免疫逃避策略,阻碍了对感染细胞的识别并逃避了抗体反应。了解免疫机制和反应对于开发针对冠状病毒的有效疫苗和治疗方法至关重要。黏膜免疫在 COVID-19 中的作用是显著的,影响着对病毒的局部和全身免疫反应。尽管大多数临床研究集中在周围血液中的抗体和细胞免疫上,但呼吸道黏膜免疫反应在早期限制病毒复制和清除 SARS-CoV-2 方面发挥着关键作用。鉴定与病毒清除相关的黏膜生物标志物将允许监测感染诱导的免疫。正在比较和对比黏膜递送疫苗和正在临床试验中的疫苗,以了解它们在诱导针对冠状病毒的黏膜免疫方面的有效性。对肺组织免疫的更深入了解可能会导致改进诊断和预后程序以及新的治疗策略,旨在减轻社区获得性肺炎的疾病负担,避免感染的全身表现和过度发病率和死亡率。这篇综述文章概述了目前关于黏膜免疫反应在清除 SARS-CoV-2 感染中的作用的证据,以及针对(再)感染的潜在黏膜保护机制。它还提出黏膜免疫以及分泌型和循环型 IgA 抗体在 COVID-19 中起着重要作用,阐明这一点对于理解感染的无症状和轻度状态尤其重要,因为这些状态似乎占大多数病例。此外,黏膜免疫可能被用于有益的诊断、治疗或预防性目的。最近在 COVID-19 黏膜免疫方面的研究结果可用于开发有效的疫苗和治疗方法,这些方法可以有效地靶向黏膜和全身免疫反应。