Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.17/3913 |
Resumo: | SLE has a complex pathogenesis, and multiple therapeutic targets have been discovered in recent years. In spite of belimumab being approved by the US Food and Drug Administration and the widespread use of rituximab, there have been many failed attempts to treat SLE successfully using biologic agents. In this review, we consider newer biologic approaches that might offer the hope of improving the outcome of SLE patients. These include the fully humanized anti-CD20 mAbs, PEGylated anti-CD40L, IFNα inhibitors, rigerimod and immune complexes blockade. |
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Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus ErythematosusHCC DAUTOIMAntibodies, Monoclonal, Humanized / therapeutic useBiological Products / therapeutic use*HumansImmunoglobulin Fab Fragments / therapeutic useImmunologic Factors / therapeutic use*Interferon-alpha / therapeutic useLupus Erythematosus, Systemic / drug therapy*Polyethylene Glycols / therapeutic useRituximab / therapeutic useTreatment OutcomeSLE has a complex pathogenesis, and multiple therapeutic targets have been discovered in recent years. In spite of belimumab being approved by the US Food and Drug Administration and the widespread use of rituximab, there have been many failed attempts to treat SLE successfully using biologic agents. In this review, we consider newer biologic approaches that might offer the hope of improving the outcome of SLE patients. These include the fully humanized anti-CD20 mAbs, PEGylated anti-CD40L, IFNα inhibitors, rigerimod and immune complexes blockade.Oxford University PressRepositório do Centro Hospitalar Universitário de Lisboa Central, EPECarreira, PIsenberg, D2021-11-22T15:30:42Z20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/3913engRheumatology (Oxford). 2019 Mar 1;58(3):382-387.10.1093/rheumatology/key064.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:44:36Zoai:repositorio.chlc.min-saude.pt:10400.17/3913Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:13.418726Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
title |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
spellingShingle |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus Carreira, P HCC DAUTOIM Antibodies, Monoclonal, Humanized / therapeutic use Biological Products / therapeutic use* Humans Immunoglobulin Fab Fragments / therapeutic use Immunologic Factors / therapeutic use* Interferon-alpha / therapeutic use Lupus Erythematosus, Systemic / drug therapy* Polyethylene Glycols / therapeutic use Rituximab / therapeutic use Treatment Outcome |
title_short |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
title_full |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
title_fullStr |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
title_full_unstemmed |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
title_sort |
Recent Developments in Biologic Therapies for the Treatment of Patients with Systemic Lupus Erythematosus |
author |
Carreira, P |
author_facet |
Carreira, P Isenberg, D |
author_role |
author |
author2 |
Isenberg, D |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE |
dc.contributor.author.fl_str_mv |
Carreira, P Isenberg, D |
dc.subject.por.fl_str_mv |
HCC DAUTOIM Antibodies, Monoclonal, Humanized / therapeutic use Biological Products / therapeutic use* Humans Immunoglobulin Fab Fragments / therapeutic use Immunologic Factors / therapeutic use* Interferon-alpha / therapeutic use Lupus Erythematosus, Systemic / drug therapy* Polyethylene Glycols / therapeutic use Rituximab / therapeutic use Treatment Outcome |
topic |
HCC DAUTOIM Antibodies, Monoclonal, Humanized / therapeutic use Biological Products / therapeutic use* Humans Immunoglobulin Fab Fragments / therapeutic use Immunologic Factors / therapeutic use* Interferon-alpha / therapeutic use Lupus Erythematosus, Systemic / drug therapy* Polyethylene Glycols / therapeutic use Rituximab / therapeutic use Treatment Outcome |
description |
SLE has a complex pathogenesis, and multiple therapeutic targets have been discovered in recent years. In spite of belimumab being approved by the US Food and Drug Administration and the widespread use of rituximab, there have been many failed attempts to treat SLE successfully using biologic agents. In this review, we consider newer biologic approaches that might offer the hope of improving the outcome of SLE patients. These include the fully humanized anti-CD20 mAbs, PEGylated anti-CD40L, IFNα inhibitors, rigerimod and immune complexes blockade. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019 2019-01-01T00:00:00Z 2021-11-22T15:30:42Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/3913 |
url |
http://hdl.handle.net/10400.17/3913 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Rheumatology (Oxford). 2019 Mar 1;58(3):382-387. 10.1093/rheumatology/key064. |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Oxford University Press |
publisher.none.fl_str_mv |
Oxford University Press |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799131308405817344 |