Evidence map›Paper›PMID 33199847›Full record

ArticleNature biomedical engineering2021

Systemic tumour suppression via the preferential accumulation of erythrocyte-anchored chemokine-encapsulating nanoparticles in lung metastases.

Zongmin Zhao, Anvay Ukidve, Vinu Krishnan, Alexandra Fehnel, Daniel C Pan, Yongsheng Gao, Jayoung Kim, Michael A Evans, Abhirup Mandal, Junling Guo and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biomedical engineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.5field-weighted citation impact, top 4% of its field
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

51 citing papers in PubMed, 90 citations in OpenAlex.

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  15. Biomimetic erythrocyte-based drug delivery systems for organ-targeted therapy.Frontiers in bioengineering and biotechnology · 2025
    Review
  16. Cell carriers change theActa pharmaceutica Sinica. B · 2024
    Article
  17. Cell-drug conjugates.Nature biomedical engineering · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Zongmin Zhao *John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Anvay Ukidve *John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-6757-7942
Vinu KrishnanJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Alexandra FehnelJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Daniel C PanJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Yongsheng GaoJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Jayoung KimJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Michael A EvansJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Abhirup MandalJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-2543-4994
Junling GuoWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Vladimir R MuzykantovDepartment of Systems Pharmacology and Translational Therapeutics and Center for Translational Targeted Therapeutics and Nanomedicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Samir MitragotriJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA. mitragotri@seas.harvard.edu.ORCID http://orcid.org/0000-0002-2459-8305
Harvard University · USTarget (United States) · US

Funding

Vascular delivery of nanocarriers by erythrocyresR01HL143806 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MUZYKANTOV, VLADIMIR R · 2018 to 2021
$2.8M
NHLBI NIH HHS R01 HL143806
6 · The paper itself

Abstract

Eliciting immune responses against primary tumours is hampered by their immunosuppressive microenvironment and by the greater inaccessibility of deeper intratumoural cells. However, metastatic tumour cells are exposed to highly perfused and immunoactive organs, such as the lungs. Here, by taking advantage of the preferential colocalization of intravenously administered erythrocytes with metastases in the lungs, we show that treatment with chemokine-encapsulating nanoparticles that are non-covalently anchored onto the surface of injected erythrocytes results in local and systemic tumour suppression in mouse models of lung metastasis. Such erythrocyte-anchored systemic immunotherapy led to the infiltration of effector immune cells into the lungs, in situ immunization without the need for exogenous antigens, inhibition of the progression of lung metastasis, and significantly extended animal survival and systemic immunity that suppressed the growth of distant tumours after rechallenge. Erythrocyte-mediated systemic immunotherapy may represent a general and potent strategy for cancer vaccination.

Indexed as

Breast NeoplasmsChemokine CXCL10ErythrocytesLung NeoplasmsAdministration, IntravenousAnimalsCell Line, TumorErythrocyte TransfusionFemaleHumansImmunotherapyMiceNanoparticlesTumor MicroenvironmentVaccinationXenograft Model Antitumor AssaysChemokine CXCL10

Identifiers

PMID33199847
OpenAlexW3105010155

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.