生物
T细胞
免疫系统
CD8型
类病毒颗粒
同型
抗体
免疫学
体液免疫
抗原
细胞毒性T细胞
病毒学
T辅助细胞
Cd4 t细胞
细胞生物学
重组DNA
单克隆抗体
生物化学
体外
基因
作者
Marion Braun,Camilla Jandus,Patrik Maurer,Anya Hammann‐Haenni,Katrin Schwarz,Martin F. Bachmann,Daniel E. Speiser,Pedro Romero
标识
DOI:10.1002/eji.201142064
摘要
Among synthetic vaccines, virus-like particles (VLPs) are used for their ability to induce strong humoral responses. Very little is reported on VLP-based-vaccine-induced CD4(+) T-cell responses, despite the requirement of helper T cells for antibody isotype switching. Further knowledge on helper T cells is also needed for optimization of CD8(+) T-cell vaccination. Here, we analysed human CD4(+) T-cell responses to vaccination with MelQbG10, which is a Qβ-VLP covalently linked to a long peptide derived from the melanoma self-antigen Melan-A. In all analysed patients, we found strong antibody responses of mainly IgG1 and IgG3 isotypes, and concomitant Th1-biased CD4(+) T-cell responses specific for Qβ. Although less strong, comparable B- and CD4(+) T-cell responses were also found specific for the Melan-A cargo peptide. Further optimization is required to shift the response more towards the cargo peptide. Nevertheless, the data demonstrate the high potential of VLPs for inducing humoral and cellular immune responses by mounting powerful CD4(+) T-cell help.
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