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Complement C4, Infections, and Autoimmune Diseases

Complement C4, a key molecule in the complement system that is one of chief constituents of innate immunity for immediate recognition and elimination of invading microbes, plays an essential role for the functions of both classical (CP) and lectin (LP) complement pathways. Complement C4 is the most...

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Autores principales: Wang, Hongbin, Liu, Mengyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317844/
https://www.ncbi.nlm.nih.gov/pubmed/34335607
http://dx.doi.org/10.3389/fimmu.2021.694928
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author Wang, Hongbin
Liu, Mengyao
author_facet Wang, Hongbin
Liu, Mengyao
author_sort Wang, Hongbin
collection PubMed
description Complement C4, a key molecule in the complement system that is one of chief constituents of innate immunity for immediate recognition and elimination of invading microbes, plays an essential role for the functions of both classical (CP) and lectin (LP) complement pathways. Complement C4 is the most polymorphic protein in complement system. A plethora of research data demonstrated that individuals with C4 deficiency are prone to microbial infections and autoimmune disorders. In this review, we will discuss the diversity of complement C4 proteins and its genetic structures. In addition, the current development of the regulation of complement C4 activation and its activation derivatives will be reviewed. Moreover, the review will provide the updates on the molecule interactions of complement C4 under the circumstances of bacterial and viral infections, as well as autoimmune diseases. Lastly, more evidence will be presented to support the paradigm that links microbial infections and autoimmune disorders under the condition of the deficiency of complement C4. We provide such an updated overview that would shed light on current research of complement C4. The newly identified targets of molecular interaction will not only lead to novel hypotheses on the study of complement C4 but also assist to propose new strategies for targeting microbial infections, as well as autoimmune disorders.
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spelling pubmed-83178442021-07-29 Complement C4, Infections, and Autoimmune Diseases Wang, Hongbin Liu, Mengyao Front Immunol Immunology Complement C4, a key molecule in the complement system that is one of chief constituents of innate immunity for immediate recognition and elimination of invading microbes, plays an essential role for the functions of both classical (CP) and lectin (LP) complement pathways. Complement C4 is the most polymorphic protein in complement system. A plethora of research data demonstrated that individuals with C4 deficiency are prone to microbial infections and autoimmune disorders. In this review, we will discuss the diversity of complement C4 proteins and its genetic structures. In addition, the current development of the regulation of complement C4 activation and its activation derivatives will be reviewed. Moreover, the review will provide the updates on the molecule interactions of complement C4 under the circumstances of bacterial and viral infections, as well as autoimmune diseases. Lastly, more evidence will be presented to support the paradigm that links microbial infections and autoimmune disorders under the condition of the deficiency of complement C4. We provide such an updated overview that would shed light on current research of complement C4. The newly identified targets of molecular interaction will not only lead to novel hypotheses on the study of complement C4 but also assist to propose new strategies for targeting microbial infections, as well as autoimmune disorders. Frontiers Media S.A. 2021-07-14 /pmc/articles/PMC8317844/ /pubmed/34335607 http://dx.doi.org/10.3389/fimmu.2021.694928 Text en Copyright © 2021 Wang and Liu https://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) and the copyright owner(s) 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
Wang, Hongbin
Liu, Mengyao
Complement C4, Infections, and Autoimmune Diseases
title Complement C4, Infections, and Autoimmune Diseases
title_full Complement C4, Infections, and Autoimmune Diseases
title_fullStr Complement C4, Infections, and Autoimmune Diseases
title_full_unstemmed Complement C4, Infections, and Autoimmune Diseases
title_short Complement C4, Infections, and Autoimmune Diseases
title_sort complement c4, infections, and autoimmune diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317844/
https://www.ncbi.nlm.nih.gov/pubmed/34335607
http://dx.doi.org/10.3389/fimmu.2021.694928
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