Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway

Research output: Contribution to journalReviewResearchpeer-review

Standard

Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway. / Rosbjerg, Anne; Genster, Ninette; Pilely, Katrine; Garred, Peter.

In: Frontiers in Microbiology, Vol. 8, 868, 2017.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Rosbjerg, A, Genster, N, Pilely, K & Garred, P 2017, 'Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway', Frontiers in Microbiology, vol. 8, 868. https://doi.org/10.3389/fmicb.2017.00868

APA

Rosbjerg, A., Genster, N., Pilely, K., & Garred, P. (2017). Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway. Frontiers in Microbiology, 8, [868]. https://doi.org/10.3389/fmicb.2017.00868

Vancouver

Rosbjerg A, Genster N, Pilely K, Garred P. Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway. Frontiers in Microbiology. 2017;8. 868. https://doi.org/10.3389/fmicb.2017.00868

Author

Rosbjerg, Anne ; Genster, Ninette ; Pilely, Katrine ; Garred, Peter. / Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway. In: Frontiers in Microbiology. 2017 ; Vol. 8.

Bibtex

@article{f840ff88690747faae09fa1a9cfd27f6,
title = "Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway",
abstract = "The complement system is a crucial defensive network that protects the host against invading pathogens. It is part of the innate immune system and can be initiated via three pathways: the lectin, classical and alternative activation pathway. Overall the network compiles a group of recognition molecules that bind specific patterns on microbial surfaces, a group of associated proteases that initiates the complement cascade, and a group of proteins that interact in proteolytic complexes or the terminal pore-forming complex. In addition, various regulatory proteins are important for controlling the level of activity. The result is a pro-inflammatory response meant to combat foreign microbes. Microbial elimination is, however, not a straight forward procedure; pathogens have adapted to their environment by evolving a collection of evasion mechanisms that circumvent the human complement system. Complement evasion strategies features different ways of exploiting human complement proteins and moreover features different pathogen-derived proteins that interfere with the normal processes. Accumulated, these mechanisms target all three complement activation pathways as well as the final common part of the cascade. This review will cover the currently known lectin pathway evasion mechanisms and give examples of pathogens that operate these to increase their chance of invasion, survival and dissemination.",
author = "Anne Rosbjerg and Ninette Genster and Katrine Pilely and Peter Garred",
year = "2017",
doi = "10.3389/fmicb.2017.00868",
language = "English",
volume = "8",
journal = "Frontiers in Microbiology",
issn = "1664-302X",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Evasion Mechanisms Used by Pathogens to Escape the Lectin Complement Pathway

AU - Rosbjerg, Anne

AU - Genster, Ninette

AU - Pilely, Katrine

AU - Garred, Peter

PY - 2017

Y1 - 2017

N2 - The complement system is a crucial defensive network that protects the host against invading pathogens. It is part of the innate immune system and can be initiated via three pathways: the lectin, classical and alternative activation pathway. Overall the network compiles a group of recognition molecules that bind specific patterns on microbial surfaces, a group of associated proteases that initiates the complement cascade, and a group of proteins that interact in proteolytic complexes or the terminal pore-forming complex. In addition, various regulatory proteins are important for controlling the level of activity. The result is a pro-inflammatory response meant to combat foreign microbes. Microbial elimination is, however, not a straight forward procedure; pathogens have adapted to their environment by evolving a collection of evasion mechanisms that circumvent the human complement system. Complement evasion strategies features different ways of exploiting human complement proteins and moreover features different pathogen-derived proteins that interfere with the normal processes. Accumulated, these mechanisms target all three complement activation pathways as well as the final common part of the cascade. This review will cover the currently known lectin pathway evasion mechanisms and give examples of pathogens that operate these to increase their chance of invasion, survival and dissemination.

AB - The complement system is a crucial defensive network that protects the host against invading pathogens. It is part of the innate immune system and can be initiated via three pathways: the lectin, classical and alternative activation pathway. Overall the network compiles a group of recognition molecules that bind specific patterns on microbial surfaces, a group of associated proteases that initiates the complement cascade, and a group of proteins that interact in proteolytic complexes or the terminal pore-forming complex. In addition, various regulatory proteins are important for controlling the level of activity. The result is a pro-inflammatory response meant to combat foreign microbes. Microbial elimination is, however, not a straight forward procedure; pathogens have adapted to their environment by evolving a collection of evasion mechanisms that circumvent the human complement system. Complement evasion strategies features different ways of exploiting human complement proteins and moreover features different pathogen-derived proteins that interfere with the normal processes. Accumulated, these mechanisms target all three complement activation pathways as well as the final common part of the cascade. This review will cover the currently known lectin pathway evasion mechanisms and give examples of pathogens that operate these to increase their chance of invasion, survival and dissemination.

U2 - 10.3389/fmicb.2017.00868

DO - 10.3389/fmicb.2017.00868

M3 - Review

C2 - 28553281

VL - 8

JO - Frontiers in Microbiology

JF - Frontiers in Microbiology

SN - 1664-302X

M1 - 868

ER -

ID: 195290069