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MABp1 Targeting IL-1α for Moderate to Severe Hidradenitis Suppurativa Not Eligible for Adalimumab: A Randomized Study.
Kanni, Theodora; Argyropoulou, Maria; Spyridopoulos, Themistoklis; Pistiki, Aikaterini; Stecher, Michael; Dinarello, Charles A; Simard, John; Giamarellos-Bourboulis, Evangelos J.
Afiliação
  • Kanni T; Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Greece.
  • Argyropoulou M; Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Greece.
  • Spyridopoulos T; Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Greece.
  • Pistiki A; Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Greece.
  • Stecher M; XBiotech, Austin, Texas, USA.
  • Dinarello CA; Department of Medicine, The University of Colorado, Colorado, Denver, USA.
  • Simard J; XBiotech, Austin, Texas, USA.
  • Giamarellos-Bourboulis EJ; Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Greece. Electronic address: egiamarel@med.uoa.gr.
J Invest Dermatol ; 138(4): 795-801, 2018 04.
Article em En | MEDLINE | ID: mdl-29129600
Patients with moderate to severe hidradenitis suppurativa failing adalimumab therapy, or those ineligible to receive it, remain a population with an unmet need. Twenty patients not eligible for adalimumab were randomized to receive 12 weeks of blind treatment with placebo or MABp1, a true human antibody targeting IL-1α. Hidradenitis suppurativa clinical response score at week 12 was the primary endpoint. The primary endpoint was met in 10% and 60% of placebo- and MABp1-treated patients, respectively (odds ratio = 13.50, 95% confidence interval = 1.19-152.51). Clinical efficacy was maintained at 24 weeks in 0% and 40%. Improvement in the visual analog scale was reported by 20% and 85.7%, respectively, of patients failing previous anti-TNF treatment. Ultrasonography showed decreased neovascularization and lesion skin depth in the MABp1 group. MABp1 treatment was associated with decrease of circulating IL-8 and of stimulated production of IL-8 by whole blood. Whole blood production for hBD-2 was negatively associated with changes on ultrasonography in the placebo group but not in the MABp1 group. MABp1 is a promising treatment for patients with hidradenitis suppurativa not eligible for adalimumab. Inhibition of neovascularization and modulation of the production of IL-8 and hBD-2 are suggested mechanisms of action.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidradenite Supurativa / Interleucina-1alfa / Adalimumab / Anticorpos Monoclonais Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidradenite Supurativa / Interleucina-1alfa / Adalimumab / Anticorpos Monoclonais Idioma: En Ano de publicação: 2018 Tipo de documento: Article