Immunomodulation by Helminths: Intracellular Pathways and Extracellular Vesicles

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Immunomodulation by Helminths : Intracellular Pathways and Extracellular Vesicles. / Zakeri, Amin; Hansen, Eline P; Andersen, Sidsel D; Williams, Andrew R; Nejsum, Peter.

In: Frontiers in Immunology, Vol. 9, 2349, 12.10.2018.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Zakeri, A, Hansen, EP, Andersen, SD, Williams, AR & Nejsum, P 2018, 'Immunomodulation by Helminths: Intracellular Pathways and Extracellular Vesicles', Frontiers in Immunology, vol. 9, 2349. https://doi.org/10.3389/fimmu.2018.02349

APA

Zakeri, A., Hansen, E. P., Andersen, S. D., Williams, A. R., & Nejsum, P. (2018). Immunomodulation by Helminths: Intracellular Pathways and Extracellular Vesicles. Frontiers in Immunology, 9, [2349]. https://doi.org/10.3389/fimmu.2018.02349

Vancouver

Zakeri A, Hansen EP, Andersen SD, Williams AR, Nejsum P. Immunomodulation by Helminths: Intracellular Pathways and Extracellular Vesicles. Frontiers in Immunology. 2018 Oct 12;9. 2349. https://doi.org/10.3389/fimmu.2018.02349

Author

Zakeri, Amin ; Hansen, Eline P ; Andersen, Sidsel D ; Williams, Andrew R ; Nejsum, Peter. / Immunomodulation by Helminths : Intracellular Pathways and Extracellular Vesicles. In: Frontiers in Immunology. 2018 ; Vol. 9.

Bibtex

@article{61ee6ee6ed9e498cafc106b054dd8092,
title = "Immunomodulation by Helminths: Intracellular Pathways and Extracellular Vesicles",
abstract = "Helminth parasites are masters at manipulating host immune responses, using an array of sophisticated mechanisms. One of the major mechanisms enabling helminths to establish chronic infections is the targeting of pattern recognition receptors (PRRs) including toll-like receptors, C-type lectin receptors, and the inflammasome. Given the critical role of these receptors and their intracellular pathways in regulating innate inflammatory responses, and also directing adaptive immunity toward Th1 and Th2 responses, recognition of the pathways triggered and/or modulated by helminths and their products will provide detailed insights about how helminths are able to establish an immunoregulatory environment. However, helminths also target PRRs-independent mechanisms (and most likely other yet unknown mechanisms and pathways) underpinning the battery of different molecules helminths produce. Herein, the current knowledge on intracellular pathways in antigen presenting cells activated by helminth-derived biomolecules is reviewed. Furthermore, we discuss the importance of helminth-derived vesicles as a less-appreciated components released during infection, their role in activating these host intracellular pathways, and their implication in the development of new therapeutic approaches for inflammatory diseases and the possibility of designing a new generation of vaccines.",
author = "Amin Zakeri and Hansen, {Eline P} and Andersen, {Sidsel D} and Williams, {Andrew R} and Peter Nejsum",
year = "2018",
month = oct,
day = "12",
doi = "10.3389/fimmu.2018.02349",
language = "English",
volume = "9",
journal = "Frontiers in Immunology",
issn = "1664-3224",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Immunomodulation by Helminths

T2 - Intracellular Pathways and Extracellular Vesicles

AU - Zakeri, Amin

AU - Hansen, Eline P

AU - Andersen, Sidsel D

AU - Williams, Andrew R

AU - Nejsum, Peter

PY - 2018/10/12

Y1 - 2018/10/12

N2 - Helminth parasites are masters at manipulating host immune responses, using an array of sophisticated mechanisms. One of the major mechanisms enabling helminths to establish chronic infections is the targeting of pattern recognition receptors (PRRs) including toll-like receptors, C-type lectin receptors, and the inflammasome. Given the critical role of these receptors and their intracellular pathways in regulating innate inflammatory responses, and also directing adaptive immunity toward Th1 and Th2 responses, recognition of the pathways triggered and/or modulated by helminths and their products will provide detailed insights about how helminths are able to establish an immunoregulatory environment. However, helminths also target PRRs-independent mechanisms (and most likely other yet unknown mechanisms and pathways) underpinning the battery of different molecules helminths produce. Herein, the current knowledge on intracellular pathways in antigen presenting cells activated by helminth-derived biomolecules is reviewed. Furthermore, we discuss the importance of helminth-derived vesicles as a less-appreciated components released during infection, their role in activating these host intracellular pathways, and their implication in the development of new therapeutic approaches for inflammatory diseases and the possibility of designing a new generation of vaccines.

AB - Helminth parasites are masters at manipulating host immune responses, using an array of sophisticated mechanisms. One of the major mechanisms enabling helminths to establish chronic infections is the targeting of pattern recognition receptors (PRRs) including toll-like receptors, C-type lectin receptors, and the inflammasome. Given the critical role of these receptors and their intracellular pathways in regulating innate inflammatory responses, and also directing adaptive immunity toward Th1 and Th2 responses, recognition of the pathways triggered and/or modulated by helminths and their products will provide detailed insights about how helminths are able to establish an immunoregulatory environment. However, helminths also target PRRs-independent mechanisms (and most likely other yet unknown mechanisms and pathways) underpinning the battery of different molecules helminths produce. Herein, the current knowledge on intracellular pathways in antigen presenting cells activated by helminth-derived biomolecules is reviewed. Furthermore, we discuss the importance of helminth-derived vesicles as a less-appreciated components released during infection, their role in activating these host intracellular pathways, and their implication in the development of new therapeutic approaches for inflammatory diseases and the possibility of designing a new generation of vaccines.

U2 - 10.3389/fimmu.2018.02349

DO - 10.3389/fimmu.2018.02349

M3 - Review

C2 - 30369927

VL - 9

JO - Frontiers in Immunology

JF - Frontiers in Immunology

SN - 1664-3224

M1 - 2349

ER -

ID: 204303103