PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 23, 2015mAbs122 citationsOpen Access

Selective targeting of the IL23 pathway: Generation and characterization of a novel high-affinity humanized anti-IL23A antibody

View Full Paper
SSSanjaya SinghRKRachel Kroe‐BarrettKCKeith A. Canada

Key Points

Key points are not available for this paper at this time.

Abstract

Herein, we describe the generation and characterization of BI 655066, a novel, highly potent neutralizing anti-interleukin-23 (IL23) monoclonal antibody in clinical development for autoimmune conditions, including psoriasis and Crohn's disease. IL23 is a key driver of the differentiation, maintenance, and activity of a number of immune cell subsets, including T helper 17 (Th17) cells, which are believed to mediate the pathogenesis of several immune-mediated disorders. Thus, IL23 neutralization is an attractive therapeutic approach. Designing an antibody for clinical activity and convenience for the patient requires certain properties, such as high affinity, specificity, and solubility. These properties were achieved by directed design of the immunization, lead identification, and humanization procedures. Favorable substance and pharmacokinetic properties were established by biophysical assessments and studies in cynomolgus monkeys.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Singh et al. (2015) studied this question.

synapsesocial.com/papers/69dcc52b7873f5f05b133ce7https://doi.org/10.1080/19420862.2015.1032491
Ask AI
Helpful
Bookmark
Share
View Full Paper