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10.1080/1744666X.2021.1919086

http://scihub22266oqcxt.onion/10.1080/1744666X.2021.1919086
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33874829!ä!33874829

suck abstract from ncbi

pmid33874829      Expert+Rev+Clin+Immunol 2021 ; 17 (6): 601-618
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  • The role of IL-6 and IL-6 blockade in COVID-19 #MMPMID33874829
  • Potere N; Batticciotto A; Vecchie A; Porreca E; Cappelli A; Abbate A; Dentali F; Bonaventura A
  • Expert Rev Clin Immunol 2021[Jun]; 17 (6): 601-618 PMID33874829show ga
  • INTRODUCTION: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a dysregulated hyperinflammatory response. AREAS COVERED: Authors review evidence on IL-6 and IL-6 blockade in coronavirus disease 2019 (COVID-19) and discuss the pathophysiological and prognostic roles of this cytokine and the clinical impact of pharmacological blockade of IL-6 . The material includes original articles and reviews published from March 2020 to March 2021 and searched on PubMed, medRxiv, and bioRxiv. EXPERT OPINION: IL-6 is one of the most prominent pro-inflammatory cytokines. Increased levels are recorded in COVID-19 patients, especially those with severe-to-critical disease. Evidence is accumulating on the relevance of IL-6 as a prognostic marker in COVID-19. Since IL-6 is a druggable target for several inflammatory diseases, pharmacological blockers of the IL-6 signaling pathway were repurposed to blunt the abnormal SARS-CoV-2-induced cytokine release. Data are limited to few randomized controlled trials that reported encouraging, though not conclusive, results, indicating the usefulness of IL-6 blockade early in the course of the disease in patients with hyperinflammation and no or limited organ damage. Further research is warranted to explore the role of IL-6 in different COVID-19 phenotypes and identify subgroups of patients who may mostly benefit from IL-6 pathway inhibition.
  • |*COVID-19 Drug Treatment[MESH]
  • |Animals[MESH]
  • |Anti-Inflammatory Agents/adverse effects/*therapeutic use[MESH]
  • |COVID-19/immunology/virology[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Interleukin-6/*antagonists & inhibitors/metabolism[MESH]
  • |Receptors, Interleukin-6/*antagonists & inhibitors/metabolism[MESH]
  • |SARS-CoV-2/immunology/*pathogenicity[MESH]
  • |Signal Transduction[MESH]


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