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Colchicine reduces the activation of NLRP3 inflammasome in COVID-19 patients.
Amaral, N B; Rodrigues, T S; Giannini, M C; Lopes, M I; Bonjorno, L P; Menezes, P I S O; Dib, S M; Gigante, S L G; Benatti, M N; Rezek, U C; Emrich-Filho, L L; Sousa, B A; Almeida, S C L; Luppino-Assad, R; Veras, F P; Schneider, A H; Leiria, L O S; Cunha, L D; Alves-Filho, J C; Cunha, T M; Arruda, E; Miranda, C H; Pazin-Filho, A; Auxiliadora-Martins, M; Borges, M C; Fonseca, B A L; Bollela, V R; Del-Ben, C M; Cunha, F Q; Santana, R C; Vilar, F C; Zamboni, D S; Louzada-Junior, P; Oliveira, R D R.
  • Amaral NB; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Rodrigues TS; Department of Cell Biology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Giannini MC; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Lopes MI; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Bonjorno LP; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Menezes PISO; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Dib SM; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Gigante SLG; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Benatti MN; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Rezek UC; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Emrich-Filho LL; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Sousa BA; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Almeida SCL; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Luppino-Assad R; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Veras FP; Department of Pharmacology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Schneider AH; Department of Pharmacology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Leiria LOS; Department of Pharmacology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Cunha LD; Department of Cell Biology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Alves-Filho JC; Department of Pharmacology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Cunha TM; Department of Pharmacology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Arruda E; Department of Cell Biology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Miranda CH; Department of Emergency Medicine, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Pazin-Filho A; Department of Emergency Medicine, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Auxiliadora-Martins M; Department of Surgery and Anatomy, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Borges MC; Department of Emergency Medicine, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Fonseca BAL; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Bollela VR; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Del-Ben CM; Department of Neuroscience and Behavior Ribeirao Preto Medical School, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Cunha FQ; Department of Pharmacology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Santana RC; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Vilar FC; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Zamboni DS; Department of Cell Biology, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • Louzada-Junior P; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil.
  • Oliveira RDR; Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14.048-900, São Paulo, Brazil. renedroliveira@gmail.com.
Inflamm Res ; 72(5): 895-899, 2023 May.
Article in English | MEDLINE | ID: covidwho-2249415
ABSTRACT

OBJECTIVE:

To evaluate whether colchicine treatment was associated with the inhibition of NLRP3 inflammasome activation in patients with COVID-19.

METHODS:

We present a post hoc analysis from a double-blinded placebo-controlled randomized clinical trial (RCT) on the effect of colchicine for the treatment of COVID-19. Serum levels of NOD-like receptor protein 3 (NLRP3) inflammasome products-active caspase-1 (Casp1p20), IL-1ß, and IL-18-were assessed at enrollment and after 48-72 h of treatment in patients receiving standard-of-care (SOC) plus placebo vs. those receiving SOC plus colchicine. The colchicine regimen was 0.5 mg tid for 5 days, followed by 0.5 mg bid for another 5 days.

RESULTS:

Thirty-six patients received SOC plus colchicine, and thirty-six received SOC plus placebo. Colchicine reduced the need for supplemental oxygen and the length of hospitalization. On Days 2-3, colchicine lowered the serum levels of Casp1p20 and IL-18, but not IL-1ß.

CONCLUSION:

Treatment with colchicine inhibited the activation of the NLRP3 inflammasome, an event triggering the 'cytokine storm' in COVID-19. TRIAL REGISTRATION NUMBERS RBR-8jyhxh.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Inflammasomes / COVID-19 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Inflamm Res Journal subject: Allergy and Immunology / Pathology Year: 2023 Document Type: Article Affiliation country: S00011-023-01718-y

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Inflammasomes / COVID-19 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Inflamm Res Journal subject: Allergy and Immunology / Pathology Year: 2023 Document Type: Article Affiliation country: S00011-023-01718-y