Evidence map›Paper›PMID 42661925›Full record

ArticleFrontiers in immunology2026

3D chemotaxis chip for investigating natural killer cell migration mechanisms.

Madison N Temples, Suzanne Lightsey, Tiffany Conklin, Rylee S Newport, Edward A Phelps, Blanka Sharma

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Madison N Temples *J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.
Suzanne Lightsey *J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.
Tiffany ConklinJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.
Rylee S NewportJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.
Edward A PhelpsJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.
Blanka SharmaJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.

Funding

Local immune modulation for beta cell replacement therapy in type 1 diabetesR01DK132387 · NIDDK · UNIVERSITY OF FLORIDA · PI PHELPS, EDWARD, RUSS, HOLGER A. · 2022 to 2025
$2.1M
Mechanism and dynamics of islet GABA signalingR01DK124267 · NIDDK · UNIVERSITY OF FLORIDA · PI PHELPS, EDWARD · 2021 to 2025
$1.8M
NIDDK NIH HHS R01 DK124267NIDDK NIH HHS R01 DK132387
6 · The paper itself

Abstract

Introduction: Natural killer (NK) cells are a promising tool for cancer immunotherapy, as they can rapidly recognize and kill cancer cells without prior knowledge of tumor-specific antigens while leaving healthy cells unharmed. However, a major challenge in NK cell-based therapies is their inadequate infiltration and function within solid tumors. Advancements in NK cell therapies for solid malignancies require an understanding of the various factors that influence NK cell migration to and within the tumor microenvironment. Methods: In this study, we developed a chemotaxis chip with a tunable 3D hydrogel that enabled the spatiotemporal analysis of NK cell migration. Through live-cell imaging and cell-tracking analysis, we quantitatively assessed NK cell migration in engineered hydrogels in real time. This platform enabled precise control over matrix composition and physical properties, allowing systematic interrogation of microenvironmental features that regulate NK cell migration. Results: Our findings revealed that NK cells rely heavily on proteasedependent infiltration but can leverage alternative mechanisms for faster migration, and that the inclusion of hyaluronic acid, a tumorrelated extracellular matrix component, promotes NK cell migration in 3D. Discussion: This study established an adaptable hydrogel-based platform for studying immune cell migration in defined 3D environments, providing foundational tools for future mechanistic and translational investigations.

Indexed as

Cell MovementChemotaxisKiller Cells, NaturalLab-On-A-Chip DevicesAnimalsHumansHyaluronic AcidHydrogelsTumor MicroenvironmentHyaluronic AcidHydrogelsbiomaterialscancer immunotherapycell migrationnatural killer cellsthree-dimensionaltumor microenvironment

Identifiers

PMID42661925
PMCPMC13518586

What OpenQuestion holds

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Registered trials

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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.