Literature DB >> 20430307

Anti-p40 antibodies ustekinumab and briakinumab: blockade of interleukin-12 and interleukin-23 in the treatment of psoriasis.

Mona Gandhi1, Eihab Alwawi, Kenneth B Gordon.   

Abstract

The choice of therapeutic agents for patients with moderate-to-severe psoriasis has expanded significantly in the past decade. With new understanding of the immunologic basis of psoriasis, multiple new potential targets for therapy have been identified. It is likely that a series of new medications to focus on the newly identified pathways is on the horizon. The first pathway targeted by new medications focuses on the p40 subunit that is shared by interleukin (IL)-12 and IL-23. Two human anti-p40 antibodies have been used therapeutically in psoriasis to date, ustekinumab (CNTO-1275, Stelara, Centocor, Horsham, PA) and briakinumab (ABT-874, Abbott, Abbott Park, IL). Ustekinumab was recently approved by the United States Food and Drug Administration, making it the first medication approved in the United States to work by this pathway while briakinumab is currently in phase III clinical trials.

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Year:  2010        PMID: 20430307     DOI: 10.1016/j.sder.2010.02.001

Source DB:  PubMed          Journal:  Semin Cutan Med Surg        ISSN: 1085-5629


  26 in total

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Review 2.  Pharmacokinetic de-risking tools for selection of monoclonal antibody lead candidates.

Authors:  Miroslav Dostalek; Thomayant Prueksaritanont; Robert F Kelley
Journal:  MAbs       Date:  2017-05-02       Impact factor: 5.857

Review 3.  CCR6 as a possible therapeutic target in psoriasis.

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Authors:  Ernest H Choy; Arthur F Kavanaugh; Simon A Jones
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Authors:  Charlotte Lahoute; Olivier Herbin; Ziad Mallat; Alain Tedgui
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Review 8.  Biological products for the treatment of psoriasis: therapeutic targets, pharmacodynamics and disease-drug-drug interaction implications.

Authors:  Jie Wang; Yow-Ming C Wang; Hae-Young Ahn
Journal:  AAPS J       Date:  2014-07-04       Impact factor: 4.009

9.  Target-independent variable region mediated effects on antibody clearance can be FcRn independent.

Authors:  Ryan L Kelly; Yao Yu; Tingwan Sun; Isabelle Caffry; Heather Lynaugh; Michael Brown; Tushar Jain; Yingda Xu; K Dane Wittrup
Journal:  MAbs       Date:  2016-09-09       Impact factor: 5.857

10.  Anti-interleukin-12/23p40 antibody attenuates chronic rejection of cardiac allografts partly via inhibition γδT cells.

Authors:  S Wang; X Xu; A Xie; J Li; P Ye; Z Liu; J Wu; L Rui; J Xia
Journal:  Clin Exp Immunol       Date:  2012-09       Impact factor: 4.330

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