» Articles » PMID: 20107924

Current Views on the Roles of Th1 and Th17 Cells in Experimental Autoimmune Encephalomyelitis

Overview
Date 2010 Jan 29
PMID 20107924
Citations 109
Authors
Affiliations
Soon will be listed here.
Abstract

Multiple sclerosis (MS) and its animal model, experimental autoimmune encephalomyelitis (EAE), are autoimmune demyelinating diseases of the central nervous system (CNS). Interferon-gamma-producing Th1 and interleukin-17-producing Th17 CD4(+) T helper (Th) cells mediate disease pathogenesis in EAE and likely in MS as well. However, the relative contribution of each Th subset to autoimmune processes in the CNS remains unclear. Emerging data suggest that both Th1 and Th17 cells contribute to CNS autoimmunity, albeit through different mechanisms. A better understanding of the roles that Th1 and Th17 cells play in autoimmune inflammation will be helpful in developing new therapeutic approaches. In this review, we discuss recent findings on the roles of Th1 and Th17 cells in the pathogenesis of EAE.

Citing Articles

Slow Subcutaneous Release of Glatiramer Acetate or CD40-Targeting Peptide KGYY Is More Advantageous in Treating Ongoing Experimental Autoimmune Encephalomyelitis.

Vaitaitis G, Wagner Jr D Neurol Int. 2024; 16(6):1540-1551.

PMID: 39585073 PMC: 11587089. DOI: 10.3390/neurolint16060114.


Formyl peptide receptor 2 regulates dendritic cell metabolism and Th17 cell differentiation during neuroinflammation.

Lim J, Neuwirth A, Chung K, Grossklaus S, Soehnlein O, Hajishengallis G Front Immunol. 2024; 15:1354074.

PMID: 39148732 PMC: 11324504. DOI: 10.3389/fimmu.2024.1354074.


2-Bromo-1,4-Naphthalenedione promotes CD8 T cell expansion and limits Th1/Th17 to mitigate experimental autoimmune encephalomyelitis.

Yang C, Ma Y, Lu Q, Qu Y, Li Y, Cheng S J Neuroinflammation. 2024; 21(1):181.

PMID: 39068463 PMC: 11283727. DOI: 10.1186/s12974-024-03172-x.


Dietary protection against the visual and motor deficits induced by experimental autoimmune encephalomyelitis.

Zyla-Jackson K, Walton D, Plafker K, Kovats S, Georgescu C, Brush R Front Neurol. 2023; 14:1113954.

PMID: 36937529 PMC: 10017782. DOI: 10.3389/fneur.2023.1113954.


Transcriptional inhibition of STAT1 functions in the nucleus alleviates Th1 and Th17 cell-mediated inflammatory diseases.

Park J, Son M, Ho C, Lee S, Kim Y, An J Front Immunol. 2023; 13:1054472.

PMID: 36591260 PMC: 9800178. DOI: 10.3389/fimmu.2022.1054472.


References
1.
OConnor Jr W, Kamanaka M, Booth C, Town T, Nakae S, Iwakura Y . A protective function for interleukin 17A in T cell-mediated intestinal inflammation. Nat Immunol. 2009; 10(6):603-9. PMC: 2709990. DOI: 10.1038/ni.1736. View

2.
Veldhoen M, Hocking R, Atkins C, Locksley R, Stockinger B . TGFbeta in the context of an inflammatory cytokine milieu supports de novo differentiation of IL-17-producing T cells. Immunity. 2006; 24(2):179-89. DOI: 10.1016/j.immuni.2006.01.001. View

3.
Kuchroo V, Anderson A, Waldner H, Munder M, Bettelli E, Nicholson L . T cell response in experimental autoimmune encephalomyelitis (EAE): role of self and cross-reactive antigens in shaping, tuning, and regulating the autopathogenic T cell repertoire. Annu Rev Immunol. 2002; 20:101-23. DOI: 10.1146/annurev.immunol.20.081701.141316. View

4.
Park H, Li Z, Yang X, Chang S, Nurieva R, Wang Y . A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17. Nat Immunol. 2005; 6(11):1133-41. PMC: 1618871. DOI: 10.1038/ni1261. View

5.
Gran B, Zhang G, Yu S, Li J, Chen X, Ventura E . IL-12p35-deficient mice are susceptible to experimental autoimmune encephalomyelitis: evidence for redundancy in the IL-12 system in the induction of central nervous system autoimmune demyelination. J Immunol. 2002; 169(12):7104-10. DOI: 10.4049/jimmunol.169.12.7104. View