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基于肽的癌症疫苗的合成递送制剂的设计与评估

Design and Evaluation of Synthetic Delivery Formulations for Peptide-Based Cancer Vaccines.

作者信息

Song Kefan, Pun Suzie H

机构信息

Department of Bioengineering, University of Washington, USA.

Molecular Engineering & Sciences Institute, University of Washington, USA.

出版信息

BME Front. 2024 Mar 21;5:0038. doi: 10.34133/bmef.0038. eCollection 2024.

DOI:10.34133/bmef.0038
PMID:38515636
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10956738/
Abstract

With the recent advances in neoantigen identification, peptide-based cancer vaccines offer substantial potential in the field of immunotherapy. However, rapid clearance, low immunogenicity, and insufficient antigen-presenting cell (APC) uptake limit the efficacy of peptide-based cancer vaccines. This review explores the barriers hindering vaccine efficiency, highlights recent advancements in synthetic delivery systems, and features strategies for the key delivery steps of lymph node (LN) drainage, APC delivery, cross-presentation strategies, and adjuvant incorporation. This paper also discusses the design of preclinical studies evaluating vaccine efficiency, including vaccine administration routes and murine tumor models.

摘要

随着新抗原鉴定技术的最新进展,基于肽的癌症疫苗在免疫治疗领域具有巨大潜力。然而,快速清除、低免疫原性以及抗原呈递细胞(APC)摄取不足限制了基于肽的癌症疫苗的疗效。本综述探讨了阻碍疫苗效率的障碍,强调了合成递送系统的最新进展,并介绍了淋巴结(LN)引流、APC递送、交叉呈递策略和佐剂掺入等关键递送步骤的策略。本文还讨论了评估疫苗效率的临床前研究设计,包括疫苗给药途径和小鼠肿瘤模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/1a572745300e/bmef.0038.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/bb3f5a525e2d/bmef.0038.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/c979553ec8a6/bmef.0038.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/1a572745300e/bmef.0038.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/bb3f5a525e2d/bmef.0038.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/c979553ec8a6/bmef.0038.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06db/10956738/1a572745300e/bmef.0038.fig.003.jpg

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CD8 T cells maintain killing of MHC-I-negative tumor cells through the NKG2D-NKG2DL axis.CD8 T 细胞通过 NKG2D-NKG2DL 轴维持对 MHC-I 阴性肿瘤细胞的杀伤。
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Perforin-2 is a pore-forming effector of endocytic escape in cross-presenting dendritic cells.
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