Literature DB >> 23433455

Protein therapeutics targeted at the TNF superfamily.

Carl F Ware1.   

Abstract

Protein-based drugs with their unequivocal specificity achieved the long sought milestone of selectively disrupting cytokine pathways to alleviate ongoing inflammation. Tumor necrosis factor (TNF), a member of the superfamily of cytokines involved in regulating immune and inflammatory processes, provides an exemplary model of protein therapeutics. Antibody and receptor-based inhibitors of TNF modify inflammation leading to dramatic improvement in patients with certain autoimmune diseases. Collectively, the structure, specificity and valence of these protein-based drugs provide direct evidence that the essential mechanism of action is antagonism of the ligand-receptor interaction. Accumulating clinical knowledge regarding TNF inhibitors also provide insights into the mechanisms involved in different autoimmune diseases. Experience in the development of an arsenal of biologics directed at TNF has additionally contributed to knowledge toward overcoming the challenges of protein drugs, which include production, delivery, antigenicity and pharmacodynamics. Dramatic clinical outcomes with TNF inhibitors are driving investigation and development of biologics toward other members of the TNF superfamily to selectively alter functional properties of the immune system.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23433455     DOI: 10.1016/B978-0-12-404717-4.00002-0

Source DB:  PubMed          Journal:  Adv Pharmacol        ISSN: 1054-3589


  7 in total

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Journal:  MAbs       Date:  2016-01-11       Impact factor: 5.857

Review 2.  Lymphotoxin and TNF: how it all began-a tribute to the travelers.

Authors:  Nancy H Ruddle
Journal:  Cytokine Growth Factor Rev       Date:  2014-02-12       Impact factor: 7.638

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Authors:  Carolina Mora-Solano; Yi Wen; Huifang Han; Jianjun Chen; Anita S Chong; Michelle L Miller; Rebecca R Pompano; Joel H Collier
Journal:  Biomaterials       Date:  2017-09-26       Impact factor: 12.479

4.  Dimerization of LTβR by LTα1β2 is necessary and sufficient for signal transduction.

Authors:  Jawahar Sudhamsu; Jianping Yin; Eugene Y Chiang; Melissa A Starovasnik; Jane L Grogan; Sarah G Hymowitz
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-18       Impact factor: 11.205

5.  BAFF-neutralizing interaction of belimumab related to its therapeutic efficacy for treating systemic lupus erythematosus.

Authors:  Woori Shin; Hyun Tae Lee; Heejin Lim; Sang Hyung Lee; Ji Young Son; Jee Un Lee; Ki-Young Yoo; Seong Eon Ryu; Jaejun Rhie; Ju Yeon Lee; Yong-Seok Heo
Journal:  Nat Commun       Date:  2018-03-23       Impact factor: 14.919

6.  Fluorescence Correlation Spectroscopy Reveals Efficient Cytosolic Delivery of Protein Cargo by Cell-Permeant Miniature Proteins.

Authors:  Rebecca F Wissner; Angela Steinauer; Susan L Knox; Alexander D Thompson; Alanna Schepartz
Journal:  ACS Cent Sci       Date:  2018-09-27       Impact factor: 14.553

7.  Characterization of B- and T-Cell Compartment and B-Cell Related Factors Belonging to the TNF/TNFR Superfamily in Patients With Clinically Active Systemic Lupus Erythematosus: Baseline BAFF Serum Levels Are the Strongest Predictor of Response to Belimumab after Twelve Months of Therapy.

Authors:  Silvia Piantoni; Francesca Regola; Stefania Masneri; Michele Merletti; Torsten Lowin; Paolo Airò; Angela Tincani; Franco Franceschini; Laura Andreoli; Georg Pongratz
Journal:  Front Pharmacol       Date:  2021-05-21       Impact factor: 5.810

  7 in total

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