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Complement System Part II: Role in Immunity
The complement system has been considered for a long time as a simple lytic cascade, aimed to kill bacteria infecting the host organism. Nowadays, this vision has changed and it is well accepted that complement is a complex innate immune surveillance system, playing a key role in host homeostasis, i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443744/ https://www.ncbi.nlm.nih.gov/pubmed/26074922 http://dx.doi.org/10.3389/fimmu.2015.00257 |
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author | Merle, Nicolas S. Noe, Remi Halbwachs-Mecarelli, Lise Fremeaux-Bacchi, Veronique Roumenina, Lubka T. |
author_facet | Merle, Nicolas S. Noe, Remi Halbwachs-Mecarelli, Lise Fremeaux-Bacchi, Veronique Roumenina, Lubka T. |
author_sort | Merle, Nicolas S. |
collection | PubMed |
description | The complement system has been considered for a long time as a simple lytic cascade, aimed to kill bacteria infecting the host organism. Nowadays, this vision has changed and it is well accepted that complement is a complex innate immune surveillance system, playing a key role in host homeostasis, inflammation, and in the defense against pathogens. This review discusses recent advances in the understanding of the role of complement in physiology and pathology. It starts with a description of complement contribution to the normal physiology (homeostasis) of a healthy organism, including the silent clearance of apoptotic cells and maintenance of cell survival. In pathology, complement can be a friend or a foe. It acts as a friend in the defense against pathogens, by inducing opsonization and a direct killing by C5b–9 membrane attack complex and by triggering inflammatory responses with the anaphylatoxins C3a and C5a. Opsonization plays also a major role in the mounting of an adaptive immune response, involving antigen presenting cells, T-, and B-lymphocytes. Nevertheless, it can be also an enemy, when pathogens hijack complement regulators to protect themselves from the immune system. Inadequate complement activation becomes a disease cause, as in atypical hemolytic uremic syndrome, C3 glomerulopathies, and systemic lupus erythematosus. Age-related macular degeneration and cancer will be described as examples showing that complement contributes to a large variety of conditions, far exceeding the classical examples of diseases associated with complement deficiencies. Finally, we discuss complement as a therapeutic target. |
format | Online Article Text |
id | pubmed-4443744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44437442015-06-12 Complement System Part II: Role in Immunity Merle, Nicolas S. Noe, Remi Halbwachs-Mecarelli, Lise Fremeaux-Bacchi, Veronique Roumenina, Lubka T. Front Immunol Immunology The complement system has been considered for a long time as a simple lytic cascade, aimed to kill bacteria infecting the host organism. Nowadays, this vision has changed and it is well accepted that complement is a complex innate immune surveillance system, playing a key role in host homeostasis, inflammation, and in the defense against pathogens. This review discusses recent advances in the understanding of the role of complement in physiology and pathology. It starts with a description of complement contribution to the normal physiology (homeostasis) of a healthy organism, including the silent clearance of apoptotic cells and maintenance of cell survival. In pathology, complement can be a friend or a foe. It acts as a friend in the defense against pathogens, by inducing opsonization and a direct killing by C5b–9 membrane attack complex and by triggering inflammatory responses with the anaphylatoxins C3a and C5a. Opsonization plays also a major role in the mounting of an adaptive immune response, involving antigen presenting cells, T-, and B-lymphocytes. Nevertheless, it can be also an enemy, when pathogens hijack complement regulators to protect themselves from the immune system. Inadequate complement activation becomes a disease cause, as in atypical hemolytic uremic syndrome, C3 glomerulopathies, and systemic lupus erythematosus. Age-related macular degeneration and cancer will be described as examples showing that complement contributes to a large variety of conditions, far exceeding the classical examples of diseases associated with complement deficiencies. Finally, we discuss complement as a therapeutic target. Frontiers Media S.A. 2015-05-26 /pmc/articles/PMC4443744/ /pubmed/26074922 http://dx.doi.org/10.3389/fimmu.2015.00257 Text en Copyright © 2015 Merle, Noe, Halbwachs-Mecarelli, Fremeaux-Bacchi and Roumenina. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Merle, Nicolas S. Noe, Remi Halbwachs-Mecarelli, Lise Fremeaux-Bacchi, Veronique Roumenina, Lubka T. Complement System Part II: Role in Immunity |
title | Complement System Part II: Role in Immunity |
title_full | Complement System Part II: Role in Immunity |
title_fullStr | Complement System Part II: Role in Immunity |
title_full_unstemmed | Complement System Part II: Role in Immunity |
title_short | Complement System Part II: Role in Immunity |
title_sort | complement system part ii: role in immunity |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443744/ https://www.ncbi.nlm.nih.gov/pubmed/26074922 http://dx.doi.org/10.3389/fimmu.2015.00257 |
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