ReviewJournal of nanobiotechnology2026
Cell-based drug delivery for combating bacteria: focus on refractory infections.
Review in Journal of nanobiotechnology, 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
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
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
8 authors.
Funding
Abstract
The escalating crisis of antimicrobial resistance and biofilm-associated infections has fundamentally compromised conventional anti-infective therapy. Current antimicrobial agents for refractory infections face critical limitations, including systemic toxicity, inadequate tissue penetration, and the rapid emergence of multidrug resistance (MDR). As a promising strategy, cell-based drug delivery systems (CDDS) leverage living cells or their bioactive derivatives as sophisticated carriers to overcome these barriers. By harnessing innate biological functions, such as prolonged circulation, immune evasion, and active targeting, CDDS enhances therapeutic efficacy in preclinical models against refractory infections. This review systematically elaborates on CDDS platforms engineered from erythrocytes, immune cells, platelets, and stem cells, highlighting their unique mechanisms and advantages in anti-infective drug delivery. Furthermore, we critically evaluate the translational progress and future potential of CDDS in combating refractory infections, particularly those involving multidrug-resistant bacteria and biofilm-associated pathogens.
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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.