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疫苗针对黏膜淋巴组织可促进胃肠道的体液免疫。

Vaccine targeting to mucosal lymphoid tissues promotes humoral immunity in the gastrointestinal tract.

机构信息

Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Consortium for HIV/AIDS Vaccine Development (CHAVD), Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Sci Adv. 2024 May 31;10(22):eadn7786. doi: 10.1126/sciadv.adn7786. Epub 2024 May 29.


DOI:10.1126/sciadv.adn7786
PMID:38809992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11135404/
Abstract

Viruses, bacteria, and parasites frequently cause infections in the gastrointestinal tract, but traditional vaccination strategies typically elicit little or no mucosal antibody responses. Here, we report a strategy to effectively concentrate immunogens and adjuvants in gut-draining lymph nodes (LNs) to induce gut-associated mucosal immunity. We prepared nanoemulsions (NEs) based on biodegradable oils commonly used as vaccine adjuvants, which encapsulated a potent Toll-like receptor agonist and displayed antigen conjugated to their surface. Following intraperitoneal administration, these NEs accumulated in gut-draining mesenteric LNs, priming strong germinal center responses and promoting B cell class switching to immunoglobulin A (IgA). Optimized NEs elicited 10- to 1000-fold higher antigen-specific IgG and IgA titers in the serum and feces, respectively, compared to free antigen mixed with NE, and strong neutralizing antibody titers against severe acute respiratory syndrome coronavirus 2. Thus, robust gut humoral immunity can be elicited by exploiting the unique lymphatic collection pathways of the gut with a lymph-targeting vaccine formulation.

摘要

病毒、细菌和寄生虫经常引起胃肠道感染,但传统的疫苗接种策略通常只能引起很少或没有黏膜抗体的反应。在这里,我们报告了一种策略,可以有效地将免疫原和佐剂集中在肠道引流淋巴结(LNs)中,以诱导肠道相关黏膜免疫。我们制备了基于常用作疫苗佐剂的可生物降解油的纳米乳液(NEs),这些乳液中包裹了一种有效的 Toll 样受体激动剂,并在其表面展示了抗原。腹腔给药后,这些 NE 在肠道引流肠系膜淋巴结中聚集,引发强烈的生发中心反应,并促进 B 细胞类别转换为免疫球蛋白 A(IgA)。与游离抗原与 NE 混合相比,优化后的 NE 分别在血清和粪便中引起 10 到 1000 倍更高的抗原特异性 IgG 和 IgA 滴度,并且对严重急性呼吸综合征冠状病毒 2 产生强烈的中和抗体滴度。因此,通过利用肠道独特的淋巴收集途径,采用淋巴靶向疫苗制剂,可以引起强烈的肠道体液免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/457488c12fb8/sciadv.adn7786-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/c4455ecc0ea2/sciadv.adn7786-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/fcf7f65df7e0/sciadv.adn7786-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/51482a8abfd2/sciadv.adn7786-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/d734da200331/sciadv.adn7786-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/457488c12fb8/sciadv.adn7786-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/c4455ecc0ea2/sciadv.adn7786-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/fcf7f65df7e0/sciadv.adn7786-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/51482a8abfd2/sciadv.adn7786-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/d734da200331/sciadv.adn7786-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8340/11135404/457488c12fb8/sciadv.adn7786-f5.jpg

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引用本文的文献

[1]
The Current Status, Hotspots, and Development Trends of Nanoemulsions: A Comprehensive Bibliometric Review.

Int J Nanomedicine. 2025-3-11

[2]
Mucosal immune response in biology, disease prevention and treatment.

Signal Transduct Target Ther. 2025-1-8

本文引用的文献

[1]
Serotonin reduction in post-acute sequelae of viral infection.

Cell. 2023-10-26

[2]
Intranasal vaccination with lipid-conjugated immunogens promotes antigen transmucosal uptake to drive mucosal and systemic immunity.

Sci Transl Med. 2022-7-20

[3]
Preliminary phase 1 results from an HIV vaccine candidate trial.

Lancet Microbe. 2021-3

[4]
ChAdOx1-S adenoviral vector vaccine applied intranasally elicits superior mucosal immunity compared to the intramuscular route of vaccination.

Eur J Immunol. 2022-6

[5]
Preclinical evaluation of a SARS-CoV-2 mRNA vaccine PTX-COVID19-B.

Sci Adv. 2022-1-21

[6]
Aerosol delivery, but not intramuscular injection, of adenovirus-vectored tuberculosis vaccine induces respiratory-mucosal immunity in humans.

JCI Insight. 2022-2-8

[7]
"World in motion" - emulsion adjuvants rising to meet the pandemic challenges.

NPJ Vaccines. 2021-12-21

[8]
Phosphate-mediated coanchoring of RBD immunogens and molecular adjuvants to alum potentiates humoral immunity against SARS-CoV-2.

Sci Adv. 2021-12-10

[9]
Engineered SARS-CoV-2 receptor binding domain improves manufacturability in yeast and immunogenicity in mice.

Proc Natl Acad Sci U S A. 2021-9-21

[10]
Mucosal vaccines: wisdom from now and then.

Int Immunol. 2021-11-25

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