• 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

通过溶解微针递送的基于佐剂 SARS-CoV-2 刺突蛋白的微粒疫苗在小鼠中诱导体液、黏膜和细胞免疫反应。

Adjuvanted-SARS-CoV-2 Spike Protein-Based Microparticulate Vaccine Delivered by Dissolving Microneedles Induces Humoral, Mucosal, and Cellular Immune Responses in Mice.

作者信息

Patil Smital, Vijayanand Sharon, Menon Ipshita, Gomes Keegan Braz, Kale Akanksha, Bagwe Priyal, Yacoub Shadi, Uddin Mohammad N, D'Souza Martin J

机构信息

Center for Drug Delivery and Research, Vaccine Nanotechnology Laboratory, College of Pharmacy, Mercer University, Atlanta, GA 30341, USA.

出版信息

Pharmaceuticals (Basel). 2023 Aug 10;16(8):1131. doi: 10.3390/ph16081131.

DOI:10.3390/ph16081131
PMID:37631046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10457992/
Abstract

COVID-19 continues to cause an increase in the number of cases and deaths worldwide. Due to the ever-mutating nature of the virus, frequent vaccination against COVID-19 is anticipated. Most of the approved SARS-CoV-2 vaccines are administered using the conventional intramuscular route, causing vaccine hesitancy. Thus, there is a need for an effective, non-invasive vaccination strategy against COVID-19. This study evaluated the synergistic effects of a subunit microparticulate vaccine delivered using microneedles. The microparticles encapsulated a highly immunogenic subunit protein of the SARS-CoV-2 virus, such as the spike protein's receptor binding domain (RBD). Adjuvants were also incorporated to enhance the spike RBD-specific immune response. Our vaccination study reveals that a microneedle-based vaccine delivering these microparticles induced spike RBD-specific IgM, IgG, IgG1, IgG2a, and IgA antibodies. The vaccine also generated high levels of CD4+ and CD8a+ molecules in the secondary lymphoid organs. Overall, dissolving microneedles delivery spike RBD antigen in microparticulate form induced a robust immune response, paving the way for an alternative self-administrable, non-invasive vaccination strategy against COVID-19.

摘要

新冠病毒肺炎(COVID-19)在全球范围内导致的病例数和死亡人数持续增加。由于该病毒不断变异的特性,预计需要频繁接种COVID-19疫苗。大多数已获批的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗采用传统的肌肉注射途径给药,导致人们对疫苗存在犹豫。因此,需要一种针对COVID-19的有效、非侵入性的疫苗接种策略。本研究评估了使用微针递送的亚单位微粒疫苗的协同效应。这些微粒包裹了SARS-CoV-2病毒的一种高免疫原性亚单位蛋白,如刺突蛋白的受体结合域(RBD)。还加入了佐剂以增强针对刺突RBD的特异性免疫反应。我们的疫苗接种研究表明,递送这些微粒的基于微针的疫苗诱导了针对刺突RBD的特异性IgM、IgG、IgG1、IgG2a和IgA抗体。该疫苗还在二级淋巴器官中产生了高水平的CD4+和CD8a+分子。总体而言,以微粒形式溶解微针递送刺突RBD抗原可诱导强烈的免疫反应,为针对COVID-19的另一种可自我给药的非侵入性疫苗接种策略铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/7df54370cc24/pharmaceuticals-16-01131-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/d62e82d8cbbe/pharmaceuticals-16-01131-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/c8f101c7be43/pharmaceuticals-16-01131-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/66181fe92c12/pharmaceuticals-16-01131-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/180b35235107/pharmaceuticals-16-01131-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/1b42c9349659/pharmaceuticals-16-01131-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/f465f1a179d8/pharmaceuticals-16-01131-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/fed7e6a5f85d/pharmaceuticals-16-01131-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/77d3fb4e9877/pharmaceuticals-16-01131-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/7df54370cc24/pharmaceuticals-16-01131-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/d62e82d8cbbe/pharmaceuticals-16-01131-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/c8f101c7be43/pharmaceuticals-16-01131-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/66181fe92c12/pharmaceuticals-16-01131-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/180b35235107/pharmaceuticals-16-01131-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/1b42c9349659/pharmaceuticals-16-01131-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/f465f1a179d8/pharmaceuticals-16-01131-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/fed7e6a5f85d/pharmaceuticals-16-01131-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/77d3fb4e9877/pharmaceuticals-16-01131-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/10457992/7df54370cc24/pharmaceuticals-16-01131-g009.jpg

相似文献

1
Adjuvanted-SARS-CoV-2 Spike Protein-Based Microparticulate Vaccine Delivered by Dissolving Microneedles Induces Humoral, Mucosal, and Cellular Immune Responses in Mice.通过溶解微针递送的基于佐剂 SARS-CoV-2 刺突蛋白的微粒疫苗在小鼠中诱导体液、黏膜和细胞免疫反应。
Pharmaceuticals (Basel). 2023 Aug 10;16(8):1131. doi: 10.3390/ph16081131.
2
An Adjuvanted Inactivated SARS-CoV-2 Microparticulate Vaccine Delivered Using Microneedles Induces a Robust Immune Response in Vaccinated Mice.使用微针递送的佐剂灭活SARS-CoV-2微粒疫苗在接种小鼠中诱导强烈的免疫反应。
Pharmaceutics. 2023 Mar 9;15(3):895. doi: 10.3390/pharmaceutics15030895.
3
Subunit microparticulate vaccine delivery using microneedles trigger significant SARS-spike-specific humoral and cellular responses in a preclinical murine model.使用微针递送亚单位微粒疫苗可在临床前小鼠模型中引发针对 SARS 刺突蛋白的显著体液和细胞应答。
Int J Pharm. 2023 Feb 5;632:122583. doi: 10.1016/j.ijpharm.2023.122583. Epub 2023 Jan 4.
4
Characterization of Systemic and Mucosal Humoral Immune Responses to an Adjuvanted Intranasal SARS-CoV-2 Protein Subunit Vaccine Candidate in Mice.小鼠中一种佐剂鼻内接种的SARS-CoV-2蛋白亚单位候选疫苗的全身和粘膜体液免疫反应特征
Vaccines (Basel). 2022 Dec 23;11(1):30. doi: 10.3390/vaccines11010030.
5
Elicitation of potent neutralizing antibodies in obese mice by ISA 51-adjuvanted SARS-CoV-2 spike RBD-Fc vaccine.ISA 51 佐剂的 SARS-CoV-2 刺突 RBD-Fc 疫苗在肥胖小鼠中引发强烈的中和抗体反应。
Appl Microbiol Biotechnol. 2023 May;107(9):2983-2995. doi: 10.1007/s00253-023-12490-8. Epub 2023 Mar 29.
6
Oral subunit SARS-CoV-2 vaccine induces systemic neutralizing IgG, IgA and cellular immune responses and can boost neutralizing antibody responses primed by an injected vaccine.口服亚单位 SARS-CoV-2 疫苗可诱导全身中和 IgG、IgA 和细胞免疫应答,并能增强已接种疫苗产生的中和抗体应答。
Vaccine. 2022 Feb 16;40(8):1098-1107. doi: 10.1016/j.vaccine.2022.01.025. Epub 2022 Jan 19.
7
Comprehensive characterization of the antibody responses to SARS-CoV-2 Spike protein finds additional vaccine-induced epitopes beyond those for mild infection.全面描述了针对 SARS-CoV-2 刺突蛋白的抗体反应,发现了除轻度感染诱导的表位之外的其他疫苗诱导的表位。
Elife. 2022 Jan 24;11:e73490. doi: 10.7554/eLife.73490.
8
Receptor-binding domain-based SARS-CoV-2 vaccine adjuvanted with cyclic di-adenosine monophosphate enhances humoral and cellular immunity in mice.基于受体结合域的 SARS-CoV-2 疫苗与环状二腺苷单磷酸佐剂增强了小鼠的体液和细胞免疫。
J Med Virol. 2023 Feb;95(2):e28584. doi: 10.1002/jmv.28584.
9
Microneedle Delivery of an Adjuvanted Microparticulate Vaccine Induces High Antibody Levels in Mice Vaccinated against Coronavirus.佐剂微颗粒疫苗的微针递送在接种冠状病毒疫苗的小鼠中诱导产生高抗体水平。
Vaccines (Basel). 2022 Sep 7;10(9):1491. doi: 10.3390/vaccines10091491.
10
CHO-produced RBD-Fc subunit vaccines with alternative adjuvants generate immune responses against SARS-CoV-2.CHO 细胞产生的 RBD-Fc 亚单位疫苗与不同佐剂联合使用可产生针对 SARS-CoV-2 的免疫应答。
PLoS One. 2023 Jul 14;18(7):e0288486. doi: 10.1371/journal.pone.0288486. eCollection 2023.

引用本文的文献

1
Exploring the Biological Activities of Ionic Liquids and Their Potential to Develop Novel Vaccine Adjuvants.探索离子液体的生物活性及其开发新型疫苗佐剂的潜力。
Vaccines (Basel). 2025 Mar 28;13(4):365. doi: 10.3390/vaccines13040365.
2
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.
3
Delivery of PLGA-Loaded Influenza Vaccine Microparticles Using Dissolving Microneedles Induces a Robust Immune Response.

本文引用的文献

1
Dissolving Microneedles Loaded with Nanoparticle Formulation of Respiratory Syncytial Virus Fusion Protein Virus-like Particles (F-VLPs) Elicits Cellular and Humoral Immune Responses.负载呼吸道合胞病毒融合蛋白病毒样颗粒(F-VLPs)纳米颗粒制剂的可溶解微针引发细胞免疫和体液免疫反应。
Vaccines (Basel). 2023 Apr 18;11(4):866. doi: 10.3390/vaccines11040866.
2
Zika Vaccine Microparticles (MPs)-Loaded Dissolving Microneedles (MNs) Elicit a Significant Immune Response in a Pre-Clinical Murine Model.载有寨卡疫苗微粒(MPs)的溶蚀性微针(MNs)在临床前小鼠模型中引发显著的免疫反应。
Vaccines (Basel). 2023 Mar 3;11(3):583. doi: 10.3390/vaccines11030583.
3
使用溶解微针递送负载PLGA的流感疫苗微粒可诱导强烈的免疫反应。
Pharmaceutics. 2025 Apr 12;17(4):510. doi: 10.3390/pharmaceutics17040510.
4
Evaluating the Immunogenicity of an Intranasal Microparticle Combination Vaccine for COVID-19 and Influenza.评估一种用于新冠肺炎和流感的鼻内微粒联合疫苗的免疫原性。
Vaccines (Basel). 2025 Mar 7;13(3):282. doi: 10.3390/vaccines13030282.
5
The Long-Term Immunity of a Microneedle Array Patch of a SARS-CoV-2 S1 Protein Subunit Vaccine Irradiated by Gamma Rays in Mice.γ射线辐照的SARS-CoV-2 S1蛋白亚单位疫苗微针阵列贴片在小鼠体内的长期免疫
Vaccines (Basel). 2025 Jan 18;13(1):86. doi: 10.3390/vaccines13010086.
6
Polymeric Microneedle Drug Delivery Systems: Mechanisms of Treatment, Material Properties, and Clinical Applications-A Comprehensive Review.聚合物微针给药系统:治疗机制、材料特性及临床应用——综述
Polymers (Basel). 2024 Sep 11;16(18):2568. doi: 10.3390/polym16182568.
Subunit microparticulate vaccine delivery using microneedles trigger significant SARS-spike-specific humoral and cellular responses in a preclinical murine model.
使用微针递送亚单位微粒疫苗可在临床前小鼠模型中引发针对 SARS 刺突蛋白的显著体液和细胞应答。
Int J Pharm. 2023 Feb 5;632:122583. doi: 10.1016/j.ijpharm.2023.122583. Epub 2023 Jan 4.
4
Microneedle Delivery of an Adjuvanted Microparticulate Vaccine Induces High Antibody Levels in Mice Vaccinated against Coronavirus.佐剂微颗粒疫苗的微针递送在接种冠状病毒疫苗的小鼠中诱导产生高抗体水平。
Vaccines (Basel). 2022 Sep 7;10(9):1491. doi: 10.3390/vaccines10091491.
5
Assessment of In Vitro Immunostimulatory Activity of an Adjuvanted Whole-Cell Inactivated Microparticle Vaccine Formulation.佐剂全细胞灭活微粒疫苗制剂的体外免疫刺激活性评估
Vaccines (Basel). 2022 Jun 21;10(7):983. doi: 10.3390/vaccines10070983.
6
Novel microparticulate Zika vaccine induces a significant immune response in a preclinical murine model after intramuscular administration.新型微颗粒寨卡疫苗经肌肉注射后,在临床前小鼠模型中诱导出显著的免疫应答。
Int J Pharm. 2022 Aug 25;624:121975. doi: 10.1016/j.ijpharm.2022.121975. Epub 2022 Jul 3.
7
Nanoparticle formulation of the fusion protein virus like particles of respiratory syncytial virus stimulates enhanced in vitro antigen presentation and autophagy.呼吸道合胞病毒融合蛋白病毒样颗粒的纳米颗粒制剂可刺激体外增强的抗原呈递和自噬。
Int J Pharm. 2022 Jul 25;623:121919. doi: 10.1016/j.ijpharm.2022.121919. Epub 2022 Jun 15.
8
Safety, immunogenicity, and reactogenicity of BNT162b2 and mRNA-1273 COVID-19 vaccines given as fourth-dose boosters following two doses of ChAdOx1 nCoV-19 or BNT162b2 and a third dose of BNT162b2 (COV-BOOST): a multicentre, blinded, phase 2, randomised trial.BNT162b2 和 mRNA-1273 新冠疫苗作为两剂 ChAdOx1 nCoV-19 或 BNT162b2 疫苗后的第四剂加强针,以及一剂 BNT162b2 疫苗后的第三剂加强针的安全性、免疫原性和反应原性:一项多中心、盲法、2 期、随机试验。
Lancet Infect Dis. 2022 Aug;22(8):1131-1141. doi: 10.1016/S1473-3099(22)00271-7. Epub 2022 May 9.
9
Peptide-Based Vaccines and Therapeutics for COVID-19.用于治疗新冠肺炎的基于肽的疫苗和疗法
Int J Pept Res Ther. 2022;28(3):94. doi: 10.1007/s10989-022-10397-y. Epub 2022 Apr 19.
10
A dual-delivery platform for vaccination using antigen-loaded nanoparticles in dissolving microneedles.采用载抗原纳米粒的溶解微针的双重递药平台进行疫苗接种。
Int J Pharm. 2022 Feb 5;613:121393. doi: 10.1016/j.ijpharm.2021.121393. Epub 2021 Dec 17.