ReviewCurrent microbiology2025
Bloodstream Infection-induced Neuroinflammation: from Systemic Infection To Brain Invasion.
Review in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Reexamining the Role of Amyloid β Clearance from the Brain: Exporting Labile Iron from the Interstitial Fluid Performs a Protective Function.International journal of molecular sciences · 2026Review
- The eye as a gateway to the brain: mechanisms of ocular neuroinvasion by parasitic pathogens.GMS hygiene and infection control · 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
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bloodstream infections (BSIs), caused by a diverse array of microbial pathogens, have emerged as key drivers of systemic inflammation that can compromise the integrity of blood-brain barrier (BBB) and trigger neuroinflammatory responses. This review highlights the pivotal role of BSIs in initiating neuroinflammation and accelerating the progression of neurodegenerative diseases (NDDs). Literature review shows that pathogens involved in BSIs can disrupt the BBB, activate neuroglial cells, and release pro-inflammatory cytokines, ultimately causing neuronal injury and fueling chronic neuroinflammation. Clinically, survivors of BSIs, especially those who experience sepsis, face a heightened risk of long-term neurological decline. While antimicrobial treatments remain essential, advanced therapeutic options such as psychedelics, immunomodulators, and nano pharmacology, gene therapies offer promising strategies to mitigate neuroinflammation and protect brain function. The review emphasizes the urgency of early intervention, particularly in sepsis patients, to prevent the onset of chronic NDDs and preserve cognitive health. A deeper understanding of the mechanisms underlying BSI-induced neuroinflammation will be critical in developing personalized treatments to reduce the neurological burden associated with these infections. Ultimately, this review aims to provide clinicians with insights into neuroprotective strategies that have shown promise in animal models of BSIs, with the potential to improve patient outcomes if validated in humans; further clinical studies are essential to translate these findings into effective therapies for long-term neurological consequences.
Indexed as
Identifiers
41320701What 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.