ReviewNature reviews. Drug discovery2026
Microsystem technologies for accelerating the discovery and translation of immunotherapies.
Review in Nature reviews. Drug discovery, 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.
- Organization from cell to tissue derived delivery systems for immunotherapy.Materials today. Bio · 2026Article
- Engineering Organ-on-a-Chip Systems for Cancer Immunotherapy: Strategies and Assay Integration.Bioengineering (Basel, Switzerland) · 2026Review
- Optimizing next-generation CAR-macrophages against solid tumors: challenges and potential strategies.Journal of hematology & oncology · 2026Review
- A self-supplying HMaterials today. Bio · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Immunotherapies have transformed the treatment of many cancers and autoimmune diseases. However, durable therapeutic benefits are achieved in only certain subsets of patients. Due to the complexity and heterogeneity of disease, it remains challenging to design effective immunotherapies and predict their effects. Microscale systems - including microfluidics, microelectronics and microscaffolds - are now being adapted to accelerate immunotherapy discovery and development, with the potential to address efficacy, toxicity, predictability and affordability challenges. These microsystems consist of miniaturized structures, sensors and actuators that can manipulate molecules and cells of the immune system with high accuracy and throughput. Advances facilitated by microsystem technologies relevant to the discovery and translation of key types of immunotherapy (monoclonal antibodies, cytokine-based drugs, engineered immune cells and therapeutic vaccines) include the development of high-throughput devices for functional selection, miniaturized bioreactors for biomanufacturing, engineered scaffolds for therapeutic administration and sensitive biosensors for immune surveillance post-administration. Challenges facing the clinical translation of microsystem-based immunotherapies include issues related to standardization and integration as well as the need for new regulatory guidance.
Indexed as
Identifiers
40954236What 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.