Evidence map›Paper›PMID 42839014›Full record

ArticleNature biomedical engineering2026

Metal-organic framework nanovaccines for systemic tumour regression.

Xiaomin Jiang, Chaoyu Wang, Kaiting Yang, Langston Tillman, Elizabeth J Lin, András Piffkó, Chuangyu Wen, Tomas Germanas, Jinhong Li, Xin Ma and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biomedical engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Xiaomin Jiang *Department of Chemistry, School of Science, Westlake University, Hangzhou, China.ORCID http://orcid.org/0000-0001-8304-4938
Chaoyu Wang *Department of Chemistry, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-9224-5061
Kaiting YangDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL, USA.
Langston TillmanPritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, USA.
Elizabeth J LinDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0009-0002-2837-5683
András PiffkóDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-5300-6594
Chuangyu WenDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL, USA.
Tomas GermanasDepartment of Chemistry, The University of Chicago, Chicago, IL, USA.
Jinhong LiDepartment of Chemistry, The University of Chicago, Chicago, IL, USA.
Xin MaDepartment of Chemistry, The University of Chicago, Chicago, IL, USA.
Hua Laura LiangDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-5512-8595
Ralph R WeichselbaumDepartment of Chemistry, The University of Chicago, Chicago, IL, USA.
Wenbin LinDepartment of Chemistry, School of Science, Westlake University, Hangzhou, China. linwenbin@westlake.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer vaccines can elicit antigen-specific antitumour immunity, but their clinical efficacy is often limited by their inability to sustain T-cell activation in tumours. Here we report MOF-Vac, a nanoscale metal-organic framework (MOF)-based therapeutic vaccine platform that co-delivers peptide antigens and STING agonists with high loading capacity and phosphate-triggered intracellular release. This design enables coordinated antigen presentation and innate immune activation, resulting in sustained T-cell priming and intratumoural effector function. In murine models of melanoma, colorectal cancer, triple-negative breast cancer, lung cancer and oropharyngeal cancer, MOF-Vac induced tumour regression, immune memory and protection against metastasis. MOF-Vac also synergized with radiotherapy and immune checkpoint blockade to eradicate both primary and distant tumours. Single-cell RNA sequencing and immune depletion studies revealed that therapeutic efficacy predominantly depends on macrophage-mediated antigen presentation and remodelling of the tumour microenvironment towards a proinflammatory, immune-active state. MOF-Vac provides a modular platform for off-the-shelf and personalized cancer vaccination.

Identifiers

PMID42839014

What OpenQuestion holds

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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.