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