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10.3855/jidc.15386

http://scihub22266oqcxt.onion/10.3855/jidc.15386
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35192527!ä!35192527

suck abstract from ncbi


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pmid35192527      J+Infect+Dev+Ctries 2022 ; 16 (1): 101-111
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  • The potential role of the combined PARP-1 and VEGF inhibition in severe SARS-CoV-2 (COVID-19) infection #MMPMID35192527
  • Lampropoulou DI; Bala VM; Zerva E; Pliakou E; Filippou D; Gazouli M; Aravantinos G
  • J Infect Dev Ctries 2022[Jan]; 16 (1): 101-111 PMID35192527show ga
  • INTRODUCTION: During the evolution of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, several drug candidates have been proposed for repositioning towards a quest for more effective treatments. METHODOLOGY: We reviewed recent literature (Pubmed, Google, Clinicaltrials.gov), as of the middle of May 2021, for evidence regarding the potential benefit from poly(ADP-ribose)-polymerase inhibitors and vascular endothelial growth factor blockade in severe SARS-CoV-2 infection. RESULTS: poly(ADP-ribose)-polymerase inhibitors have been suggested as potential agents against coronavirus disease 2019 (COVID-19) by a variety of mechanisms. vascular endothelial growth factor-associated vascular permeability is implicated with increased vascular leakage and pulmonary oedema. Thus, anti-angiogenesis factors, such as bevacizumab are being investigated in critically ill COVID-19 patients. CONCLUSIONS: The synergistic potential of these two classes of inhibitors in severe COVID-19 management could be beneficial. Further research should be carried out in order to support this hypothesis.
  • |*COVID-19 Drug Treatment[MESH]
  • |*COVID-19/epidemiology[MESH]
  • |*Poly(ADP-ribose) Polymerase Inhibitors/pharmacology[MESH]
  • |*Vascular Endothelial Growth Factor A/pharmacology[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Patient Acuity[MESH]


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