Current progress in neoantigen-based dendritic cell vaccines for solid tumors

Immunotherapy, particularly immune checkpoint inhibitors (ICIs) programmed death-ligand 1/programmed death-1 (PD-L1/PD-1) and cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), has heralded a new era of tumor treatment. Although ICIs have clinical benefits, their complex heterogeneity and diverse...

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Published in:Cancer Biology & Medicine
Main Authors: Yuting Li, Abudukadierjiang Abudureheman, Jianming Xu
Format: Article
Language:English
Published: China Anti-Cancer Association 2025-10-01
Subjects:
Online Access:https://www.cancerbiomed.org/content/22/10/1143
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author Yuting Li
Abudukadierjiang Abudureheman
Jianming Xu
author_facet Yuting Li
Abudukadierjiang Abudureheman
Jianming Xu
author_sort Yuting Li
collection DOAJ
container_title Cancer Biology & Medicine
description Immunotherapy, particularly immune checkpoint inhibitors (ICIs) programmed death-ligand 1/programmed death-1 (PD-L1/PD-1) and cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), has heralded a new era of tumor treatment. Although ICIs have clinical benefits, their complex heterogeneity and diverse resistance mechanisms critically limit their efficacy. Neoantigens, arising from tumor-specific alterations, offer novel targets for individualized immunotherapy, because of their high immunogenicity and tumor specificity. In the past decade, neoantigen-based tumor vaccines have been demonstrated to be a promising immunotherapy strategy to prime the tumor-specific immune response. These therapeutic vaccines include peptide vaccines, nucleic acid vaccines, and dendritic cell (DC) vaccines, and are categorized according to the neoantigen source and delivery method. In vivo, neoantigens are processed and presented by antigen-presenting cells (APCs) via the peptide-Major Histocompatibility Complex (pMHC) for T cell recognition, thereby triggering specific immune responses. Because DCs, the most potent APCs, play crucial roles in antitumor immunity, neoantigen-based DC vaccines provide a promising therapeutic strategy. A series of global clinical trials are exploring the safety, feasibility, and efficacy of neoantigen-based DC vaccines in tumors. This review focuses on current progress in clinical research on neoantigen-based DC vaccines in the treatment of solid tumors.
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spelling doaj-art-0e5ab0f2e57e4e7988ddefda6064a6412025-10-23T06:02:09ZengChina Anti-Cancer AssociationCancer Biology & Medicine2095-39412025-10-0122101143115710.20892/j.issn.2095-3941.2025.0267Current progress in neoantigen-based dendritic cell vaccines for solid tumorsYuting Li0Abudukadierjiang Abudureheman1Jianming Xu2Department of Oncology, The First Medical Center, Chinese PLA General Hospital/Medical School of Chinese PLA, Beijing 100853, ChinaDepartment of Oncology, The First Medical Center, Chinese PLA General Hospital/Medical School of Chinese PLA, Beijing 100853, ChinaDepartment of Oncology, The Fifth Medical Center of the PLA General Hospital, Beijing 100071, ChinaImmunotherapy, particularly immune checkpoint inhibitors (ICIs) programmed death-ligand 1/programmed death-1 (PD-L1/PD-1) and cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), has heralded a new era of tumor treatment. Although ICIs have clinical benefits, their complex heterogeneity and diverse resistance mechanisms critically limit their efficacy. Neoantigens, arising from tumor-specific alterations, offer novel targets for individualized immunotherapy, because of their high immunogenicity and tumor specificity. In the past decade, neoantigen-based tumor vaccines have been demonstrated to be a promising immunotherapy strategy to prime the tumor-specific immune response. These therapeutic vaccines include peptide vaccines, nucleic acid vaccines, and dendritic cell (DC) vaccines, and are categorized according to the neoantigen source and delivery method. In vivo, neoantigens are processed and presented by antigen-presenting cells (APCs) via the peptide-Major Histocompatibility Complex (pMHC) for T cell recognition, thereby triggering specific immune responses. Because DCs, the most potent APCs, play crucial roles in antitumor immunity, neoantigen-based DC vaccines provide a promising therapeutic strategy. A series of global clinical trials are exploring the safety, feasibility, and efficacy of neoantigen-based DC vaccines in tumors. This review focuses on current progress in clinical research on neoantigen-based DC vaccines in the treatment of solid tumors.https://www.cancerbiomed.org/content/22/10/1143neoantigendendritic cellvaccinesimmunotherapysolid tumor
spellingShingle Yuting Li
Abudukadierjiang Abudureheman
Jianming Xu
Current progress in neoantigen-based dendritic cell vaccines for solid tumors
neoantigen
dendritic cell
vaccines
immunotherapy
solid tumor
title Current progress in neoantigen-based dendritic cell vaccines for solid tumors
title_full Current progress in neoantigen-based dendritic cell vaccines for solid tumors
title_fullStr Current progress in neoantigen-based dendritic cell vaccines for solid tumors
title_full_unstemmed Current progress in neoantigen-based dendritic cell vaccines for solid tumors
title_short Current progress in neoantigen-based dendritic cell vaccines for solid tumors
title_sort current progress in neoantigen based dendritic cell vaccines for solid tumors
topic neoantigen
dendritic cell
vaccines
immunotherapy
solid tumor
url https://www.cancerbiomed.org/content/22/10/1143
work_keys_str_mv AT yutingli currentprogressinneoantigenbaseddendriticcellvaccinesforsolidtumors
AT abudukadierjiangabudureheman currentprogressinneoantigenbaseddendriticcellvaccinesforsolidtumors
AT jianmingxu currentprogressinneoantigenbaseddendriticcellvaccinesforsolidtumors