Complement C4, Infections, and Autoimmune Diseases
Hongbin Wang1,2,3, Mengyao Liu1
1Master Program of Pharmaceutical Sciences College of Graduate Studies, California Northstate University, Elk Grove, CA, United States.
Insights
Complement C4 deficiency increases susceptibility to infections and autoimmune diseases. This review details C4 diversity, regulation, and interactions, linking C4 deficiency to these conditions and suggesting new therapeutic targets.
Area of Science:
- Immunology
- Molecular Biology
- Genetics
Background:
- Complement C4 is crucial for innate immunity and the classical/lectin complement pathways.
- C4 is the most polymorphic protein in the complement system.
- C4 deficiency is linked to increased risk of infections and autoimmune disorders.
Purpose of the Study:
- To review complement C4 protein diversity and genetic structures.
- To discuss the regulation of C4 activation and its derivatives.
- To update knowledge on C4 molecule interactions in infections and autoimmune diseases.
Main Methods:
- Literature review of existing research on complement C4.
- Analysis of genetic diversity and protein structure.
- Synthesis of data on C4 regulation and interactions.
Main Results:
- Individuals with C4 deficiency exhibit heightened susceptibility to microbial infections.
- C4 deficiency is associated with an increased prevalence of autoimmune diseases.
- Newly identified molecular interactions of C4 offer insights into disease mechanisms.
Conclusions:
- C4 deficiency links microbial infections and autoimmune disorders.
- Understanding C4 diversity and interactions is key to developing new therapeutic strategies.
- This review provides an updated overview of complement C4 research.
Abstract:
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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