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10.1016/j.intimp.2021.108125

http://scihub22266oqcxt.onion/10.1016/j.intimp.2021.108125
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suck abstract from ncbi


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pmid34543980      Int+Immunopharmacol 2021 ; 100 (ä): 108125
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  • Increased LPS levels coexist with systemic inflammation and result in monocyte activation in severe COVID-19 patients #MMPMID34543980
  • Teixeira PC; Dorneles GP; Santana Filho PC; da Silva IM; Schipper LL; Postiga IAL; Neves CAM; Rodrigues Junior LC; Peres A; Souto JT; Fonseca SG; Eller S; Oliveira TF; Rotta LN; Thompson CE; Romao PRT
  • Int Immunopharmacol 2021[Nov]; 100 (ä): 108125 PMID34543980show ga
  • Mucosal barrier alterations may play a role in the pathogenesis of several diseases, including COVID-19. In this study we evaluate the association between bacterial translocation markers and systemic inflammation at the earliest time-point after hospitalization and at the last 72 h of hospitalization in survivors and non-survivors COVID-19 patients. Sixty-six SARS-CoV-2 RT-PCR positive patients and nine non-COVID-19 pneumonia controls were admitted in this study. Blood samples were collected at hospital admission (T1) (Controls and COVID-19 patients) and 0-72 h before hospital discharge (T2, alive or dead) to analyze systemic cytokines and chemokines, lipopolysaccharide (LPS) concentrations and soluble CD14 (sCD14) levels. THP-1 human monocytic cell line was incubated with plasma from survivors and non-survivors COVID-19 patients and their phenotype, activation status, TLR4, and chemokine receptors were analyzed by flow cytometry. COVID-19 patients presented higher IL-6, IFN-gamma, TNF-alpha, TGF-beta1, CCL2/MCP-1, CCL4/MIP-1beta, and CCL5/RANTES levels than controls. Moreover, LPS and sCD14 were higher at hospital admission in SARS-CoV-2-infected patients. Non-survivors COVID-19 patients had increased LPS levels concomitant with higher IL-6, TNF-alpha, CCL2/MCP-1, and CCL5/RANTES levels at T2. Increased expression of CD16 and CCR5 were identified in THP-1 cells incubated with the plasma of survivor patients obtained at T2. The incubation of THP-1 with T2 plasma of non-survivors COVID-19 leads to higher TLR4, CCR2, CCR5, CCR7, and CD69 expression. In conclusion, the coexistence of increased microbial translocation and hyperinflammation in patients with severe COVID-19 may lead to higher monocyte activation, which may be associated with worsening outcomes, such as death.
  • |*SARS-CoV-2[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Bacterial Translocation[MESH]
  • |COVID-19/*immunology/mortality[MESH]
  • |Female[MESH]
  • |Hospitalization[MESH]
  • |Humans[MESH]
  • |Inflammation Mediators/blood[MESH]
  • |Inflammation/*etiology[MESH]
  • |Lipopolysaccharides/*blood[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Monocytes/*physiology[MESH]
  • |Severity of Illness Index[MESH]


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