Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway.
Anne Rosbjerg1, Ninette Genster1, Katrine Pilely1
1Laboratory of Molecular Medicine, Department of Clinical Immunology, Section 7631, Rigshospitalet, Faculty of Health and Medical Sciences, University of CopenhagenCopenhagen, Denmark.
Frontiers in Microbiology
|May 30, 2017
Summary
Pathogens evade the human complement system, a key innate immunity defense, using sophisticated strategies. This review details how microbes exploit complement proteins, focusing on lectin pathway evasion mechanisms.
Area of Science:
- Immunology
- Microbiology
Background:
- The complement system is a vital part of innate immunity, defending against pathogens through three activation pathways: lectin, classical, and alternative.
- Pathogens have evolved evasion mechanisms to circumvent complement-mediated host defense, targeting all activation pathways and the terminal cascade.
Purpose of the Study:
- To review known microbial evasion strategies targeting the human complement system.
- To focus specifically on evasion mechanisms of the lectin complement pathway.
- To provide examples of pathogens employing these evasion tactics.
Main Methods:
- Literature review of scientific publications.
- Analysis of pathogen-derived proteins and their interactions with the complement system.
- Categorization of evasion strategies based on targeted complement pathways.
Main Results:
- Pathogens utilize diverse strategies to subvert complement activation, including direct interference with complement proteins and pathways.
- Specific examples of pathogens and their unique complement evasion mechanisms are presented.
- Evasion strategies effectively enhance pathogen survival, invasion, and dissemination.
Conclusions:
- Understanding complement evasion is crucial for developing new therapeutic strategies against infectious diseases.
- The lectin pathway is a significant target for pathogen evasion, highlighting its importance in host defense.
- Further research into pathogen-complement interactions can reveal novel targets for antimicrobial interventions.
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