Your browser doesn't support javascript.
loading
Comparable Immune Function Inhibition by the Infliximab Biosimilar CT-P13: Implications for Treatment of Inflammatory Bowel Disease.
Lim, Ki Jung; Lee, So Jung; Kim, Sunghwan; Lee, Su Yeon; Lee, Min Seob; Park, Yoon A; Choi, Eun Jin; Lee, Eun Beom; Jun, Hwang Keun; Cho, Jong Moon; Lee, SooYoung; Kwon, Ki Sung; Lim, Byung Pil; Jeon, Myung-Shin; Shin, Eui Cheol; Choi, Yong Sung; Fudim, Ella; Picard, Orit; Yavzori, Miri; Ben-Horin, Shomron; Chang, Shin Jae.
Afiliación
  • Lim KJ; R&D Division, Celltrion Inc., Incheon, Korea.
  • Lee SJ; R&D Division, Celltrion Inc., Incheon, Korea.
  • Kim S; R&D Division, Celltrion Inc., Incheon, Korea.
  • Lee SY; R&D Division, Celltrion Inc., Incheon, Korea.
  • Lee MS; R&D Division, Celltrion Inc., Incheon, Korea.
  • Park YA; R&D Division, Celltrion Inc., Incheon, Korea.
  • Choi EJ; R&D Division, Celltrion Inc., Incheon, Korea.
  • Lee EB; R&D Division, Celltrion Inc., Incheon, Korea.
  • Jun HK; R&D Division, Celltrion Inc., Incheon, Korea.
  • Cho JM; R&D Division, Celltrion Inc., Incheon, Korea.
  • Lee S; R&D Division, Celltrion Inc., Incheon, Korea.
  • Kwon KS; R&D Division, Celltrion Inc., Incheon, Korea.
  • Lim BP; R&D Division, Celltrion Inc., Incheon, Korea.
  • Jeon MS; Translational Research Center and Inha Research Institute for Medical Sciences, Inha University School of Medicine, Incheon, Korea.
  • Shin EC; Laboratory of Immunology and Infectious Disease, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Korea.
  • Choi YS; Department of Gastroenterology, Daehang Hospital, Seoul, Korea.
  • Fudim E; Department of Gastroenterology, Sheba Medical Center & Sackler School of Medicine, Tel-Aviv University, Ramat-Gan, Israel.
  • Picard O; Department of Gastroenterology, Sheba Medical Center & Sackler School of Medicine, Tel-Aviv University, Ramat-Gan, Israel.
  • Yavzori M; Department of Gastroenterology, Sheba Medical Center & Sackler School of Medicine, Tel-Aviv University, Ramat-Gan, Israel.
  • Ben-Horin S; Department of Gastroenterology, Sheba Medical Center & Sackler School of Medicine, Tel-Aviv University, Ramat-Gan, Israel.
  • Chang SJ; R&D Division, Celltrion Inc., Incheon, Korea.
J Crohns Colitis ; 11(5): 593-602, 2017 May 01.
Article en En | MEDLINE | ID: mdl-28453766
BACKGROUND AND AIMS: CT-P13 is the first biosimilar monoclonal antibody to infliximab, and was recently approved in the European Union, Japan, Korea, and USA for all six indications of infliximab. However, studies directly assessing the biologic activity of CT-P13 versus inflximab in the context of inflammatory bowel disease [IBD] are still scanty. In the present study, we aimed to compare the biological activities of CT-P13 and infliximab with specific focus on intestinal cells so as to gain insight into the potential biosimilarity of these two agents for treatment of IBD. METHODS: CT-P13 and infliximab were investigated and compared by in vitro experiments for their neutralisation ability of soluble tumour necrosis factor alpha [sTNFα] and membrane-bound tumour necrosis factor alpha [mTNFα], suppression of cytokine release by reverse signalling, induction of regulatory macrophages and wound healing, and antibody-dependent cell cytotoxicity [ADCC]. RESULTS: CT-P13 showed similar biological activities to infliximab as gauged by neutralisation of soluble TNFα, as well as blockade of apoptosis and suppression of pro-inflammatory cytokines in intestinal Caco-2 cells. Infliximab and CT-P13 equally induced apoptosis and outside-to-inside signals through transmembrane TNFα [tmTNFα]. Moreover, regulatory macrophage induction and ensuing wound healing were similarly exerted by CT-P13 and infliximab. However, neither CT-P13 nor infliximab exerted any significant ADCC of ex vivo-stimulated peripheral blood monocytes or lamina propria mononuclear cells from IBD patients. CONCLUSIONS: These findings indicate that CT-P13 and infliximab exert highly similar biological activities in intestinal cells, and further support a mechanistic comparability of these two drugs in the treatment of IBD.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Gastrointestinales / Enfermedades Inflamatorias del Intestino / Biosimilares Farmacéuticos / Infliximab / Intestinos / Anticuerpos Monoclonales Límite: Humans Idioma: En Revista: J Crohns Colitis Asunto de la revista: GASTROENTEROLOGIA Año: 2017 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Gastrointestinales / Enfermedades Inflamatorias del Intestino / Biosimilares Farmacéuticos / Infliximab / Intestinos / Anticuerpos Monoclonales Límite: Humans Idioma: En Revista: J Crohns Colitis Asunto de la revista: GASTROENTEROLOGIA Año: 2017 Tipo del documento: Article Pais de publicación: Reino Unido