Extracellular vesicle-inspired liposomes boost immune response against pathogen antigens.

Publication date: Jun 25, 2026

Developing effective vaccines against some diseases remains a global health priority. However, targeting immunity against a specific disease-related antigen requires efficient adjuvant systems that adequately promote vaccination efficacy. Extracellular vesicles have been identified as a potential adjuvant platform technology but are still limited in their reproducibility and safety. Here, we present a synthetic extracellular vesicle mimetic (EVM) platform that enhances antigen immunogenicity by incorporating the large extracellular loop (LEL) of the tetraspanin CD9, a protein abundant on natural extracellular vesicles. Liposomes with defined lipid composition were functionalized with recombinant CD9-LEL and pathogen antigens-KMP-11 from Leishmania and the SARS-CoV-2 Spike (S) protein. BALB/c mice were immunized intraperitoneally with nanovesicles carrying CD9-LEL, the pathogen antigens alone, or both. Antigen-specific IgG responses were measured by ELISA, and vesicle uptake by immune cells was assessed via flow cytometry. CD9-LEL alone did not elicit an immune response, but its co-presentation with antigens significantly enhanced specific anti-pathogen IgG titers. Notably, KMP-11 alone failed to induce detectable antibodies, while nanovesicles carrying both CD9-LEL and KMP-11 triggered strong IgG1 and IgG2b responses. Similarly, nCD9 + S induced higher IgG titers than S alone. CD9-LEL promoted uptake of nanovesicles by peritoneal macrophages, suggesting improved antigen presentation. Combining EVMs with classical adjuvants further modulated the immune profile: alum favored IgG1 (Th2 bias), while CpG ODNs enhanced IgG2a and IgG2b (Th1 bias), crucial for intracellular pathogen clearance. The platform demonstrated safety and adaptability. In conclusion, CD9-LEL-decorated EVMs represent a promising, scalable vaccine strategy capable of boosting antigen immunogenicity and directing immune polarization, offering a versatile tool for combating challenging or emergent infectious diseases.

Concepts Keywords
Cd9 CD9
Classical Extracellular vesicles
Efficient Leishmania
Nanovesicles Nanovesicles
Vaccines Vaccine

Semantics

Type Source Name
disease MESH infectious diseases

Original Article

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