Cargando…
Complement-targeted therapy: development of C5- and C5a-targeted inhibition
The complement system is a major effector of humoral immunity and natural immunity. The complement system has three independent pathways of complement activation: a classical pathway, an alternative pathway, and a lectin pathway. These pathways converge to a common pathway that activates C3. This pa...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725830/ https://www.ncbi.nlm.nih.gov/pubmed/29259684 http://dx.doi.org/10.1186/s41232-016-0013-6 |
_version_ | 1783285612467453952 |
---|---|
author | Horiuchi, Takahiko Tsukamoto, Hiroshi |
author_facet | Horiuchi, Takahiko Tsukamoto, Hiroshi |
author_sort | Horiuchi, Takahiko |
collection | PubMed |
description | The complement system is a major effector of humoral immunity and natural immunity. The complement system has three independent pathways of complement activation: a classical pathway, an alternative pathway, and a lectin pathway. These pathways converge to a common pathway that activates C3. This pathway also leads to the formation of various bioactive molecules such as C5a and the formation of membrane attack complex on the surface of target cells. In the past, the only preparations with anti-complementary action were C1 inhibitors (C1-INH), but an anti-C5 monoclonal antibody (eculizumab) appeared a few years ago, and this antibody has yielded encouraging results. In addition, a C5a receptor (C5aR) antagonist is in the clinical trial phase, and this antagonist should also prove efficacious. Anti-complement agents have garnered attention as a new treatment strategy for refractory inflammatory diseases. |
format | Online Article Text |
id | pubmed-5725830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57258302017-12-19 Complement-targeted therapy: development of C5- and C5a-targeted inhibition Horiuchi, Takahiko Tsukamoto, Hiroshi Inflamm Regen Review The complement system is a major effector of humoral immunity and natural immunity. The complement system has three independent pathways of complement activation: a classical pathway, an alternative pathway, and a lectin pathway. These pathways converge to a common pathway that activates C3. This pathway also leads to the formation of various bioactive molecules such as C5a and the formation of membrane attack complex on the surface of target cells. In the past, the only preparations with anti-complementary action were C1 inhibitors (C1-INH), but an anti-C5 monoclonal antibody (eculizumab) appeared a few years ago, and this antibody has yielded encouraging results. In addition, a C5a receptor (C5aR) antagonist is in the clinical trial phase, and this antagonist should also prove efficacious. Anti-complement agents have garnered attention as a new treatment strategy for refractory inflammatory diseases. BioMed Central 2016-06-03 /pmc/articles/PMC5725830/ /pubmed/29259684 http://dx.doi.org/10.1186/s41232-016-0013-6 Text en © Horiuchi and Tsukamoto 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Horiuchi, Takahiko Tsukamoto, Hiroshi Complement-targeted therapy: development of C5- and C5a-targeted inhibition |
title | Complement-targeted therapy: development of C5- and C5a-targeted inhibition |
title_full | Complement-targeted therapy: development of C5- and C5a-targeted inhibition |
title_fullStr | Complement-targeted therapy: development of C5- and C5a-targeted inhibition |
title_full_unstemmed | Complement-targeted therapy: development of C5- and C5a-targeted inhibition |
title_short | Complement-targeted therapy: development of C5- and C5a-targeted inhibition |
title_sort | complement-targeted therapy: development of c5- and c5a-targeted inhibition |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725830/ https://www.ncbi.nlm.nih.gov/pubmed/29259684 http://dx.doi.org/10.1186/s41232-016-0013-6 |
work_keys_str_mv | AT horiuchitakahiko complementtargetedtherapydevelopmentofc5andc5atargetedinhibition AT tsukamotohiroshi complementtargetedtherapydevelopmentofc5andc5atargetedinhibition |