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Novel therapeutic agents in clinical development for systemic lupus erythematosus

Conventional immunosuppressive therapies have radically transformed patient survival in systemic lupus erythematosus (SLE), but their use is associated with considerable toxicity and a substantial proportion of patients remain refractory to treatment. A more comprehensive understanding of the comple...

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Detalles Bibliográficos
Autores principales: Jordan, Natasha, Lutalo, Pamela MK, D’Cruz, David P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667088/
https://www.ncbi.nlm.nih.gov/pubmed/23642011
http://dx.doi.org/10.1186/1741-7015-11-120
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author Jordan, Natasha
Lutalo, Pamela MK
D’Cruz, David P
author_facet Jordan, Natasha
Lutalo, Pamela MK
D’Cruz, David P
author_sort Jordan, Natasha
collection PubMed
description Conventional immunosuppressive therapies have radically transformed patient survival in systemic lupus erythematosus (SLE), but their use is associated with considerable toxicity and a substantial proportion of patients remain refractory to treatment. A more comprehensive understanding of the complexity of SLE immunopathogenesis has evolved over the past decade and has led to the testing of several biologic agents in clinical trials. There is a clear need for new therapeutic agents that overcome these issues, and biologic agents offer exciting prospects as future SLE therapies. An array of promising new therapies are currently emerging or are under development including B-cell depletion therapies, agents targeting B-cell survival factors, blockade of T-cell co-stimulation and anti-cytokine therapies, such as monoclonal antibodies against interleukin-6 and interferon-α.
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spelling pubmed-36670882013-06-05 Novel therapeutic agents in clinical development for systemic lupus erythematosus Jordan, Natasha Lutalo, Pamela MK D’Cruz, David P BMC Med Review Conventional immunosuppressive therapies have radically transformed patient survival in systemic lupus erythematosus (SLE), but their use is associated with considerable toxicity and a substantial proportion of patients remain refractory to treatment. A more comprehensive understanding of the complexity of SLE immunopathogenesis has evolved over the past decade and has led to the testing of several biologic agents in clinical trials. There is a clear need for new therapeutic agents that overcome these issues, and biologic agents offer exciting prospects as future SLE therapies. An array of promising new therapies are currently emerging or are under development including B-cell depletion therapies, agents targeting B-cell survival factors, blockade of T-cell co-stimulation and anti-cytokine therapies, such as monoclonal antibodies against interleukin-6 and interferon-α. BioMed Central 2013-05-03 /pmc/articles/PMC3667088/ /pubmed/23642011 http://dx.doi.org/10.1186/1741-7015-11-120 Text en Copyright © 2013 Jordan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Jordan, Natasha
Lutalo, Pamela MK
D’Cruz, David P
Novel therapeutic agents in clinical development for systemic lupus erythematosus
title Novel therapeutic agents in clinical development for systemic lupus erythematosus
title_full Novel therapeutic agents in clinical development for systemic lupus erythematosus
title_fullStr Novel therapeutic agents in clinical development for systemic lupus erythematosus
title_full_unstemmed Novel therapeutic agents in clinical development for systemic lupus erythematosus
title_short Novel therapeutic agents in clinical development for systemic lupus erythematosus
title_sort novel therapeutic agents in clinical development for systemic lupus erythematosus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667088/
https://www.ncbi.nlm.nih.gov/pubmed/23642011
http://dx.doi.org/10.1186/1741-7015-11-120
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