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Early changes in gene expression and inflammatory proteins in systemic juvenile idiopathic arthritis patients on canakinumab therapy.
Brachat, Arndt H; Grom, Alexei A; Wulffraat, Nico; Brunner, Hermine I; Quartier, Pierre; Brik, Riva; McCann, Liza; Ozdogan, Huri; Rutkowska-Sak, Lidia; Schneider, Rayfel; Gerloni, Valeria; Harel, Liora; Terreri, Maria; Houghton, Kristin; Joos, Rik; Kingsbury, Daniel; Lopez-Benitez, Jorge M; Bek, Stephan; Schumacher, Martin; Valentin, Marie-Anne; Gram, Hermann; Abrams, Ken; Martini, Alberto; Lovell, Daniel J; Nirmala, Nanguneri R; Ruperto, Nicolino.
Afiliação
  • Brachat AH; Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Grom AA; Cincinnati Children's Hospital Medical Center, PRCSG, Cincinnati, OH, USA.
  • Wulffraat N; Wilhelmina Kinderziekenhuis, Department of Pediatric Immunology and Rheumatology, Utrecht, Netherlands.
  • Brunner HI; Cincinnati Children's Hospital Medical Center, PRCSG, Cincinnati, OH, USA.
  • Quartier P; Université Paris-Descartes, IMAGINE Institute, Hôpital Necker-Enfants Malades. Centre de référence national pour les Arthrites Juveniles, Unité d'Immunologie, Hématologie et Rhumatologie Pediatrique, Paris, France.
  • Brik R; Rambam Medical Center, Department of Pediatrics B, Haifa, Israel.
  • McCann L; Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Ozdogan H; Cerrahpasa Tip Fakultesi, Ic Hastaliklari ABD, Romatoloji BD, Istanbul, Turkey.
  • Rutkowska-Sak L; Institute of Rheumatology, Paediatric Clinic, Warsaw, Poland.
  • Schneider R; Hospital for Sick Children, Division of Rheumatology, Toronto, ON, Canada.
  • Gerloni V; Istituto Gaetano Pini, Divisione di Reumatologia, Milano, Italy.
  • Harel L; Schneider Childrens Medical Center, Pediatric Rheumatology Unit, Petach-Tikvah, Israel.
  • Terreri M; Universidade Federal de São Paulo, Pediatrics, São Paulo, Brazil.
  • Houghton K; British Columbia Children's Hospital, Vancouver, BC, Canada.
  • Joos R; Universitair Ziekenhuis Gent, Centrum Voor Kinderreumatologie, Gent, Belgium.
  • Kingsbury D; Randall Children's Hospital at Legacy Emanuel, Portland, OR, USA.
  • Lopez-Benitez JM; Floating Hospital for Children, Rheumatology NEMC 286, Boston, MA, USA.
  • Bek S; Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Schumacher M; Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Valentin MA; Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Gram H; Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Abrams K; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Martini A; University of Genova and Istituto Giannina Gaslini, Pediatria II-PRINTO, Genoa, Italy.
  • Lovell DJ; Cincinnati Children's Hospital Medical Center, PRCSG, Cincinnati, OH, USA.
  • Nirmala NR; Novartis Institutes for Biomedical Research, Cambridge, MA, USA.
  • Ruperto N; Istituto Giannina Gaslini, Pediatria II-PRINTO, Genoa, Italy. nicolaruperto@gaslini.org.
Arthritis Res Ther ; 19(1): 13, 2017 01 23.
Article em En | MEDLINE | ID: mdl-28115015
ABSTRACT

BACKGROUND:

Canakinumab is a human anti-interleukin-1ß (IL-1ß) monoclonal antibody neutralizing IL-1ß-mediated pathways. We sought to characterize the molecular response to canakinumab and evaluate potential markers of response using samples from two pivotal trials in systemic juvenile idiopathic arthritis (SJIA).

METHODS:

Gene expression was measured in patients with febrile SJIA and in matched healthy controls by Affymetrix DNA microarrays. Transcriptional response was assessed by gene expression changes from baseline to day 3 using adapted JIA American College of Rheumatology (aACR) response criteria (50 aACR JIA). Changes in pro-inflammatory cytokines IL-6 and IL-18 were assessed up to day 197.

RESULTS:

Microarray analysis identified 984 probe sets differentially expressed (≥2-fold difference; P < 0.05) in patients versus controls. Over 50% of patients with ≥50 aACR JIA were recognizable by baseline expression values. Analysis of gene expression profiles from patients achieving ≥50 aACR JIA response at day 15 identified 102 probe sets differentially expressed upon treatment (≥2-fold difference; P < 0.05) on day 3 versus baseline, including IL-1ß, IL-1 receptors (IL1-R1 and IL1-R2), IL-1 receptor accessory protein (IL1-RAP), and IL-6. The strongest clinical response was observed in patients with higher baseline expression of dysregulated genes and a strong transcriptional response on day 3. IL-6 declined by day 3 (≥8-fold decline; P < 0.0001) and remained suppressed. IL-18 declined on day 57 (≥1.5-fold decline, P ≤ 0.002).

CONCLUSIONS:

Treatment with canakinumab in SJIA patients resulted in downregulation of innate immune response genes and reductions in IL-6 and clinical symptoms. Additional research is needed to investigate potential differences in the disease mechanisms in patients with heterogeneous gene transcription profiles. TRIAL REGISTRATION Clinicaltrials.gov NCT00886769 (trial 1). Registered on 22 April 2009; NCT00889863 (trial 2). Registered on 21 April 2009.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Interleucina-6 / Interleucina-18 / Transcriptoma / Anticorpos Monoclonais Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Interleucina-6 / Interleucina-18 / Transcriptoma / Anticorpos Monoclonais Idioma: En Ano de publicação: 2017 Tipo de documento: Article