ReviewACS omega2026
MXenes at the Immune Interface: A Perspective on Influence of Physicochemical Design in Immunomodulation.
Review in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
MXenes are a recently discovered family of two-dimensional (2D) transition metal-based nanomaterials, known for their compositional diversity, exceptional tunability, structural versatility, and surface functionality. Beyond their well-established application in energy storage, MXenes have attracted growing interest for their promising role in regenerative biomedicine, particularly in antimicrobial and immune engineering applications. Recent studies, including contributions from our group, demonstrate that MXenes exhibit unique interactions with immune cells and associated immunosuppressive functions. Notably, MXene nanosheets and derived quantum dots can be tailored to modulate key immunosuppressive mechanisms, including the enhancement of regulatory T-cells (Tregs), reduction of proinflammatory cytokines, macrophages modulation and autophagy induction. These findings position MXenes as potential next-generation platform for immunomodulatory therapy, either as standalone agents or in combination with existing immunosuppressants. In this perspective, we systematically examine how physiochemical parameters including size, dimension, morphology, surface chemistry, and functionalization govern their interactions with innate and adaptive system. We highlight recent advances in MXene-mediated immunomodulation, paving a roadmap for further investigations, by identifying key knowledge gaps and translational challenges. We further outline future research directions necessary to bridge the divide between experimental studies, artificial intelligence (AI)-driven optimization/predictive approaches, and clinical applications of MXene-based immunotherapies.
Identifiers
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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.