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Renal Injury in DENV-4 Fatal Cases: Viremia, Immune Response and Cytokine Profile. | LitMetric

AI Article Synopsis

  • - Dengue virus (DENV) can cause mild symptoms or lead to severe disease, including organ failure, with renal involvement linked to higher mortality rates.
  • - Post-mortem studies of four patients who died from DENV-4 in Brazil revealed significant renal damage, characterized by inflammation, tissue injury, and viral replication indicated by NS3 protein presence.
  • - The observed kidney damage likely resulted from a combination of high viral loads and an intense immune response, leading to increased secretion of inflammatory substances in the kidneys.

Article Abstract

Dengue virus (DENV) infections may result in asymptomatic cases or evolve into a severe disease, which involves multiple organ failure. Renal involvement in dengue can be potentially related to an increased mortality. Aiming to better understand the role of DENV in renal injury observed in human fatal cases, post-mortem investigations were performed in four DENV-4 renal autopsies during dengue epidemics in Brazil. Tissues were submitted to histopathology, immunohistochemistry, viral quantification, and characterization of cytokines and inflammatory mediators. Probably due the high viral load, several lesions were observed in the renal tissue, such as diffuse mononuclear infiltration around the glomerulus in the cortical region and in the medullary vessels, hyalinosis arteriolar, lymphocytic infiltrate, increased capsular fibrosis, proximal convoluted tubule (PCT) damage, edema, PCT debris formation, and thickening of the basal vessel membrane. These changes were associated with DENV-4 infection, as confirmed by the presence of DENV-specific NS3 protein, indicative of viral replication. The exacerbated presence of mononuclear cells at several renal tissue sites culminated in the secretion of proinflammatory cytokines and chemokines. Moreover, it can be suggested that the renal tissue injury observed here may have been due to the combination of both high viral load and exacerbated host immune response.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963280PMC
http://dx.doi.org/10.3390/pathogens8040223DOI Listing

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