Frequency and Focus of in Vitro Studies of Microglia-Expressed Cytokines in Response to Viral Infection: A Systematic Review.
Diego A Barrios-GonzálezSantiago Philibert-RosasIris E Martínez-JuárezFernando Sotelo-DíazVerónica Rivas-AlonsoJulio SoteloMario A Sebastián-DíazPublished in: Cellular and molecular neurobiology (2024)
It is well known that as part of their response to infectious agents such as viruses, microglia transition from a quiescent state to an activated state that includes proinflammatory and anti-inflammatory phases; this behavior has been described through in vitro studies. However, recent in vivo studies on the function of microglia have questioned the two-phase paradigm; therefore, a change in the frequency of in vitro studies is expected. A systematic review was carried out to identify the microglial cytokine profile against viral infection that has been further evaluated through in vitro studies (pro-inflammatory or anti-inflammatory), along with analysis of its publication frequency over the years. For this review, 531 articles published in the English language were collected from PubMed, Web of Science, EBSCO and ResearchGate. Only 27 papers met the inclusion criteria for this systematic review. In total, 19 cytokines were evaluated in these studies, most of which are proinflammatory; the most common are IL-6, followed by TNF-α and IL-1β. It should be pointed out that half of the studies were published between 2015 and 2022 (raw data available in https://github.com/dadriba05/SystematicReview.git ). In this review, we identified that evaluation of pro-inflammatory cytokines released by microglia against viral infections has been performed more frequently than that of anti-inflammatory cytokines; additionally, a higher frequency of evaluation of the response of microglia cells to viral infection through in vitro studies from 2015 and beyond was noted.
Keyphrases
- case control
- systematic review
- inflammatory response
- anti inflammatory
- neuropathic pain
- autism spectrum disorder
- randomized controlled trial
- rheumatoid arthritis
- meta analyses
- sars cov
- spinal cord
- cell death
- cell proliferation
- signaling pathway
- electronic health record
- big data
- cell cycle arrest
- pi k akt
- endoplasmic reticulum stress