ReviewLab on a chip2026
Lymphatics-on-a-chip microphysiological system: engineering lymphatic structure and function
Review in Lab on a chip, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 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
4 citing papers in PubMed.
- Using Organoids to Unlock the Potential of Human Torpor for Spaceflight.Current stem cell reports · 2026Article
- Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Review
- Next-generation models for lymphoid malignancies: the rise of 3D culture systems in translational hematology.British journal of cancer · 2026Review
- Engineering and Integrating Blood Vessel Organoids: a Comprehensive Blueprint for Physiological and Disease Modeling.Stem cell reviews and reports · 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
2 authors.
Funding
Abstract
The lymphatic system-integral to fluid balance, immune surveillance, and lipid absorption-is frequently overlooked despite its vital roles. Traditional research modalities, including static two-dimensional cultures and animal models, have illuminated key molecular and cellular features but fall short in recapitulating human lymphatic function, due to limited physiological relevance, throughput, and mechanobiological complexity. Recent advances in microfluidic organ-on-a-chip systems offer biomimetic platforms that integrate three-dimensional architecture, fluid flow, and biomechanical stimuli alongside human lymphatic endothelial and supporting cells. These lymphatics-on-a-chip constructs faithfully reproduce dynamic behaviors such as fluid drainage, junction remodeling, and cell trafficking under physiological and pathological responses. This review highlights the foundational lymphatic biology and engineering principles behind these devices, their capacity for disease modeling and drug testing, and their potential to drive future innovation through induced pluripotent stem cell integration, organ-specific customization, and computational modeling. Merging bioengineering, cell biology, and machine learning, lymphatic microphysiological systems stand poised to significantly expand our understanding and treatment of lymphatic-related disorders.
Indexed as
Identifiers
What OpenQuestion holds
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.