IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain.

Standard

IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain. / Tzartos, John S; Craner, Matthew J; Friese, Manuel A.; Jakobsen, Karen B; Newcombe, Jia; Esiri, Margaret M; Fugger, Lars.

In: AM J PATHOL, Vol. 178, No. 2, 2, 2011, p. 794-802.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Tzartos, JS, Craner, MJ, Friese, MA, Jakobsen, KB, Newcombe, J, Esiri, MM & Fugger, L 2011, 'IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain.', AM J PATHOL, vol. 178, no. 2, 2, pp. 794-802. <http://www.ncbi.nlm.nih.gov/pubmed/21281812?dopt=Citation>

APA

Tzartos, J. S., Craner, M. J., Friese, M. A., Jakobsen, K. B., Newcombe, J., Esiri, M. M., & Fugger, L. (2011). IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain. AM J PATHOL, 178(2), 794-802. [2]. http://www.ncbi.nlm.nih.gov/pubmed/21281812?dopt=Citation

Vancouver

Tzartos JS, Craner MJ, Friese MA, Jakobsen KB, Newcombe J, Esiri MM et al. IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain. AM J PATHOL. 2011;178(2):794-802. 2.

Bibtex

@article{debc499e1c744941b85cb3372ff604ed,
title = "IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain.",
abstract = "IL-17-producing CD4(+) T cells (Th-17) contribute to the pathogenesis of experimental autoimmune encephalomyelitis and are associated with active disease in multiple sclerosis (MS). In addition to IL-17, Th-17 cells can also express IL-21, IL-22, and IL-6 under Th-17-polarizing conditions (IL-6 and transforming growth factor- ). In this study we investigated IL-21 and IL-21 receptor (IL-21R) expression in MS lesions by in situ hybridization and immunohistochemistry. We detected strongly IL-21(+) infiltrating cells predominantly in acute but also in chronic active white matter MS lesions in which IL-21 expression was restricted to CD4(+) cells. In contrast, IL-21R was much more broadly distributed on CD4(+), CD19(+), and CD8(+) lymphocytes but not major histocompatibility complex class-II(+) macrophages/microglia. Interestingly, in cortical areas we detected both IL-21 and IL-21R expression by neurons. These findings suggest role(s) for IL-21 in both the acute and chronic stages of MS via direct effects on T and B lymphocytes and, demonstrated for the first time, also on neurons.",
author = "Tzartos, {John S} and Craner, {Matthew J} and Friese, {Manuel A.} and Jakobsen, {Karen B} and Jia Newcombe and Esiri, {Margaret M} and Lars Fugger",
year = "2011",
language = "Deutsch",
volume = "178",
pages = "794--802",
journal = "AM J PATHOL",
issn = "0002-9440",
publisher = "Elsevier Inc.",
number = "2",

}

RIS

TY - JOUR

T1 - IL-21 and IL-21 receptor expression in lymphocytes and neurons in multiple sclerosis brain.

AU - Tzartos, John S

AU - Craner, Matthew J

AU - Friese, Manuel A.

AU - Jakobsen, Karen B

AU - Newcombe, Jia

AU - Esiri, Margaret M

AU - Fugger, Lars

PY - 2011

Y1 - 2011

N2 - IL-17-producing CD4(+) T cells (Th-17) contribute to the pathogenesis of experimental autoimmune encephalomyelitis and are associated with active disease in multiple sclerosis (MS). In addition to IL-17, Th-17 cells can also express IL-21, IL-22, and IL-6 under Th-17-polarizing conditions (IL-6 and transforming growth factor- ). In this study we investigated IL-21 and IL-21 receptor (IL-21R) expression in MS lesions by in situ hybridization and immunohistochemistry. We detected strongly IL-21(+) infiltrating cells predominantly in acute but also in chronic active white matter MS lesions in which IL-21 expression was restricted to CD4(+) cells. In contrast, IL-21R was much more broadly distributed on CD4(+), CD19(+), and CD8(+) lymphocytes but not major histocompatibility complex class-II(+) macrophages/microglia. Interestingly, in cortical areas we detected both IL-21 and IL-21R expression by neurons. These findings suggest role(s) for IL-21 in both the acute and chronic stages of MS via direct effects on T and B lymphocytes and, demonstrated for the first time, also on neurons.

AB - IL-17-producing CD4(+) T cells (Th-17) contribute to the pathogenesis of experimental autoimmune encephalomyelitis and are associated with active disease in multiple sclerosis (MS). In addition to IL-17, Th-17 cells can also express IL-21, IL-22, and IL-6 under Th-17-polarizing conditions (IL-6 and transforming growth factor- ). In this study we investigated IL-21 and IL-21 receptor (IL-21R) expression in MS lesions by in situ hybridization and immunohistochemistry. We detected strongly IL-21(+) infiltrating cells predominantly in acute but also in chronic active white matter MS lesions in which IL-21 expression was restricted to CD4(+) cells. In contrast, IL-21R was much more broadly distributed on CD4(+), CD19(+), and CD8(+) lymphocytes but not major histocompatibility complex class-II(+) macrophages/microglia. Interestingly, in cortical areas we detected both IL-21 and IL-21R expression by neurons. These findings suggest role(s) for IL-21 in both the acute and chronic stages of MS via direct effects on T and B lymphocytes and, demonstrated for the first time, also on neurons.

M3 - SCORING: Zeitschriftenaufsatz

VL - 178

SP - 794

EP - 802

JO - AM J PATHOL

JF - AM J PATHOL

SN - 0002-9440

IS - 2

M1 - 2

ER -