ReviewClinical and experimental medicine2026
Innovative combinatory approaches with dendritic cell-based vaccines: bridging preclinical insights and clinical challenges.
Review in Clinical and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- The State-of-the Art of Personalized Vaccines for Non-Communicable Diseases: A Narrative Review.Vaccines · 2026Review
- Vaccine Adjuvants and Delivery Systems: A Comprehensive Review.International journal of molecular sciences · 2026Review
- Immunotherapy role in bladder cancer treatment: a review of literature.Frontiers in oncology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dendritic cell (DC)-based vaccines have emerged as a promising and innovative approach in the immunotherapy of both solid tumors and hematologic malignancies. Owing to their unique capacity to present antigens and activate tumor-specific T cell responses, DC vaccines play a pivotal role in counteracting tumor immune evasion. Despite significant advances in vaccine development, several challenges - including the immunosuppressive tumor microenvironment, the complexities of designing optimal vaccines, and the difficulty of translating preclinical successes into consistent clinical outcomes - have limited their widespread effectiveness. This review highlights recent combinatory strategies aimed at enhancing the design and application of DC-based vaccines. These include the incorporation of neoantigens, tumor lysates, mRNA platforms, DC-tumor fusion constructs, and combination therapies involving immune checkpoint inhibitors and CAR-T cells. Furthermore, we examine the translational barriers that hinder the clinical implementation of these approaches and explore future directions for improving efficacy, safety, and personalization of DC vaccines. DC-based vaccines may be more effectively positioned to yield substantial and durable clinical advantages in standard oncology practice when these combinatorial strategies are integrated with rational clinical trial design, biomarker-informed patient selection, and rigorous compliance with manufacturing and regulatory standards. Ultimately, individualized and multifaceted strategies are expected to hold the greatest promise for improving therapeutic outcomes while minimizing adverse effects.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.