z-logo
open-access-imgOpen Access
A Metabolic Switch for Th17 Pathogenicity
Author(s) -
Fred P. Davis,
Yuka Kanno,
John J. O’Shea
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2015.11.033
Subject(s) - biology , gene , autoimmunity , inflammation , gene expression , interleukin 23 , pathogenicity , microbiology and biotechnology , genetics , interleukin 17 , immunology , immune system
T helper 17 (Th17) cells are critical for host defense but can also drive autoimmunity. This divergent behavior is explored by Gaublomme et al. and Wang et al., who identify inflammation-associated genes by measuring gene expression in nearly 1,000 individual Th17 cells and show that CD5L affects the expression of pro-inflammatory genes by altering lipid synthesis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom