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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Drugs in early clinical development for Systemic Lupus Erythematosus

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Author(s):
Postal, Mariana [1] ; Sinicato, Nailu Angelica [1] ; Appenzeller, Simone [1] ; Niewold, Timothy B. [2]
Total Authors: 4
Affiliation:
[1] Univ Estadual Campinas, Dept Med, Rheumatol Unit, Fac Med Sci, Campinas, SP - Brazil
[2] Mayo Clin, Dept Immunol, Div Rheumatol, 200 1st St Southwest, Guggenheim Bldg 3-42, Rochester, MN 55905 - USA
Total Affiliations: 2
Document type: Review article
Source: EXPERT OPINION ON INVESTIGATIONAL DRUGS; v. 25, n. 5, p. 573-583, MAY 2016.
Web of Science Citations: 7
Abstract

Introduction: While immunosuppressive therapy has positively impacted the prognosis of systemic lupus erythematosus (SLE), many patients still do not respond to traditional therapy. Thus, active SLE disease remains a significant problem. Furthermore, conventional immunosuppressive treatments for SLE are associated a high risk of side effects. These issues call for improvement in our current therapeutic armamentarium.Areas covered: In this review, the authors highlight the recent developments in therapies for SLE, and present an overview of drugs which are in early clinical development for SLE. There are many new therapeutic approaches being developed, including those focused on B-cell targets, T-cell downregulation, co-stimulatory blockade, anti-cytokine agents, and kinase inhibition, and Toll-like receptor inhibition. They also discuss peptide therapy as a potential method to re-establish immune tolerance, and some of the challenges ahead in developing and testing novel agents for SLE.Expert opinion: Many novel agents are currently in development for SLE, but this encouraging news is tempered by several disappointments in clinical trials and provides a timely moment to reflect on the future of therapeutic development in SLE. It seems likely that biological heterogeneity between patients is a major contributor to difficulty in drug design in SLE. (AU)

FAPESP's process: 09/06049-6 - Blood and cerebrospinal fluid biomarkers associated with structural and functional central nervous system abnormalities in Systemic lupus erythematosus
Grantee:Simone Appenzeller
Support Opportunities: Scholarships in Brazil - Young Researchers
FAPESP's process: 09/15286-1 - PREVALENCE AND FACTORS ASSOCIATED WITH THE METABOLIC SYNDROME IN YOUNG SYSTEMIC LUPUS ERYTEMATOSUS
Grantee:Nailú Angélica Sinicato Martin
Support Opportunities: Scholarships in Brazil - Scientific Initiation
FAPESP's process: 08/02917-0 - Blood and cerebrospinal fluid biomarkers associated with structural and functional central nervous system abnormalities in systemic lupus erythematosus
Grantee:Simone Appenzeller
Support Opportunities: Research Grants - Young Investigators Grants