4.7 Article

Adjuvant Activity of CpG-Oligonucleotide Administered Transcutaneously in Combination with Vaccination Using a Self-Dissolving Microneedle Patch in Mice

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VACCINES
卷 9, 期 12, 页码 -

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MDPI
DOI: 10.3390/vaccines9121480

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transcutaneous immunization; microneedle; TLR9 ligand; adjuvant; CpG-oligonucleotide

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This study investigated the transcutaneous adjuvant activity of CpG oligonucleotide (K3) in mice and found that K3 can promote B cell activation and maturation during transcutaneous immunization (TCI), resulting in a rapid increase in antigen-specific antibody titers and memory differentiation of T and B cells. Specifically, the combination of OVA and K3 doubled the number of cells in draining lymph nodes (dLN), with a significant increase in B cells, indicating the potential of K3 as a transcutaneous adjuvant for enhancing immune responses.
In this study, we investigated the mechanism of transcutaneous adjuvant activity of the CpG-oligonucleotide (K3) in mice. Transcutaneous immunization (TCI) with an ovalbumin-loaded self-dissolving microneedle patch (OVA-sdMN) and K3-loaded hydrophilic gel patch (HG) increased OVA-specific Th2- and Th1-type IgG subclass antibody titers more rapidly and strongly than those after only OVA-sdMN administration. However, the antigen-specific proliferation of OVA-specific CD4(+) T cells was similar between the OVA-only and the OVA+K3 groups. Population analysis of various immune cells in draining lymph nodes (dLNs) in the primary immune response revealed that the OVA+K3 combination doubled the number of dLN cells, with the most significant increase in B cells. Phenotypic analysis by flow cytometry revealed that B-cell activation and maturation were promoted in the OVA+K3 group, suggesting that direct B-cell activation by K3 largely contributed to the rapid increase in antigen-specific antibody titer in TCI. In the secondary immune response, a significant increase in effector T cells and effector memory T cells, and an increase in memory B cells were observed in the OVA+K3 group compared with that in the OVA-only group. Thus, K3, as a transcutaneous adjuvant, can promote the memory differentiation of T and B cells.

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