Evidence map›Paper›PMID 38424352›Full record

ArticleNature biomedical engineering2024

Neutrophils bearing adhesive polymer micropatches as a drug-free cancer immunotherapy.

Ninad Kumbhojkar, Supriya Prakash, Tatsuya Fukuta, Kwasi Adu-Berchie, Neha Kapate, Rocky An, Solomina Darko, Vineeth Chandran Suja, Kyung Soo Park, Alexander P Gottlieb and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biomedical engineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  3. Review
  4. Neutrophils in cancer.Nature reviews. Cancer · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Albumin-Bound STING Agonist Reprograms HSPCs to Antitumor Neutrophils Enhancing CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Advances in integrating biomaterials with CAR-T cells for enhancing solid tumor therapy.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
    Article
  18. Article
  19. Nanomaterials Trigger Functional Anti-Tumoral Responses in Primary Human Immune Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  20. Article
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

15 authors at 2 institutions in 2 countries.

Ninad KumbhojkarHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.ORCID http://orcid.org/0000-0002-0097-2593
Supriya PrakashHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.
Tatsuya FukutaHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.
Kwasi Adu-BerchieWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Neha KapateHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.ORCID http://orcid.org/0000-0003-4576-0014
Rocky AnHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.ORCID http://orcid.org/0000-0003-0944-1358
Solomina DarkoHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.
Vineeth Chandran SujaHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.ORCID http://orcid.org/0000-0002-3406-7655
Kyung Soo ParkHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.
Alexander P GottliebHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.
Michael Griffith BibbeyHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.ORCID http://orcid.org/0009-0002-9449-5384
Malini MukherjiWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Lily Li-Wen WangHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.
David J MooneyHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA.ORCID http://orcid.org/0000-0001-6299-1194
Samir MitragotriHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Allston, MA, USA. mitragotri@seas.harvard.edu.ORCID http://orcid.org/0000-0002-2459-8305
Harvard University · USBrigham and Women's Hospital · US

Funding

Harvard University | Faculty of Arts and Sciences (Harvard Faculty of Arts and Sciences) School of EngineeringNational Science Foundation (NSF) 1122374National Science Foundation (NSF) 2140743National Science Foundation (NSF) ECCS-2025158
6 · The paper itself

Abstract

Tumour-associated neutrophils can exert antitumour effects but can also assume a pro-tumoural phenotype in the immunosuppressive tumour microenvironment. Here we show that neutrophils can be polarized towards the antitumour phenotype by discoidal polymer micrometric 'patches' that adhere to the neutrophils' surfaces without being internalized. Intravenously administered micropatch-loaded neutrophils accumulated in the spleen and in tumour-draining lymph nodes, and activated splenic natural killer cells and T cells, increasing the accumulation of dendritic cells and natural killer cells. In mice bearing subcutaneous B16F10 tumours or orthotopic 4T1 tumours, intravenous injection of the micropatch-loaded neutrophils led to robust systemic immune responses, a reduction in tumour burden and improvements in survival rates. Micropatch-activated neutrophils combined with the checkpoint inhibitor anti-cytotoxic T-lymphocyte-associated protein 4 resulted in strong inhibition of the growth of B16F10 tumours, and in complete tumour regression in one-third of the treated mice. Micropatch-loaded neutrophils could provide a potent, scalable and drug-free approach for neutrophil-based cancer immunotherapy.

Indexed as

ImmunotherapyMice, Inbred C57BLNeutrophilsPolymersAnimalsCell Line, TumorFemaleHumansKiller Cells, NaturalMelanoma, ExperimentalMiceMice, Inbred BALB CNeoplasmsTumor MicroenvironmentPolymers

Identifiers

PMID38424352
OpenAlexW4392294919

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.