HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A novel anti-TNF scFv constructed with human antibody frameworks and antagonistic peptides.

Abstract
The introduction of TNF inhibitors has revolutionized the treatment of some chronic inflammatory diseases, e.g., rheumatoid arthritis and Crohn's disease. However, immunogenicity is one of the important mechanisms behind treatment failure, and generally, switching to another TNF inhibitor will be the first choice for patients and doctors, which results in unmet need for novel anti-TNF agents. Small antibody molecules with less number of epitope may be valuable in less immunogenicity. In this study, with the help of computer-guided molecular design, single-chain variable fragment (scFv) TSA2 was designed using consensus frameworks of human antibody variable region as scaffold to display anti-TNF antagonistic peptides. TSA2 showed evidently improved bioactivity over TSA1 (anti-TNF scFv explored before) and almost similar activity as S-Remicade (the scFv form of Remicade, anti-TNF antibody approved by FDA), especially in inhibiting TNF-induced cytotoxicity and NF-κB activation. Human antibody consensus frameworks with less immunogenicity have been used in the designing of VH domain antibody, scFv TSA1 and TSA2. A serial of TNF-related works convinced us that the novel design strategy was feasible and could be used to design inhibitors targeting more other molecules than TNF-α. More importantly, these designed inhibitors derived from computer modeling may form a virtual antibody library whose size depends on the number of candidate antagonistic peptides. It will be molecular-targeted virtual antibody library because of the specific antagonistic peptides and the potential antibodies could be determined by virtual screening and then confirmed by biologic experiments.
AuthorsShusheng Geng, Hong Chang, Weisong Qin, Ming Lv, Yan Li, Jiannan Feng, Beifen Shen
JournalImmunologic research (Immunol Res) Vol. 62 Issue 3 Pg. 377-85 (Jul 2015) ISSN: 1559-0755 [Electronic] United States
PMID26059602 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • NF-kappa B
  • Single-Chain Antibodies
  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • Infliximab
Topics
  • Amino Acid Sequence
  • Animals
  • Antibody Affinity (immunology)
  • Arthritis, Rheumatoid (therapy)
  • Cell Line
  • Crohn Disease (therapy)
  • Cytotoxicity, Immunologic (immunology)
  • Humans
  • Infliximab (immunology)
  • L Cells
  • Mice
  • Models, Molecular
  • Molecular Docking Simulation
  • Molecular Sequence Data
  • NF-kappa B (antagonists & inhibitors)
  • Single-Chain Antibodies (immunology, therapeutic use)
  • Tumor Necrosis Factor-alpha (antagonists & inhibitors, immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: