TY - JOUR
T1 - Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
AU - International Multiple Sclerosis Genetics Consortium
A2 - Ullum, Henrik
A2 - Thørner, Lise Wegner
A2 - Sellebjerg, Finn Thorup
A2 - Sørensen, Per Soelberg
N1 - Copyright © 2019, American Association for the Advancement of Science.
PY - 2019/9/27
Y1 - 2019/9/27
N2 - We analyzed genetic data of 47,429 multiple sclerosis (MS) and 68,374 control subjects and established a reference map of the genetic architecture of MS that includes 200 autosomal susceptibility variants outside the major histocompatibility complex (MHC), one chromosome X variant, and 32 variants within the extended MHC. We used an ensemble of methods to prioritize 551 putative susceptibility genes that implicate multiple innate and adaptive pathways distributed across the cellular components of the immune system. Using expression profiles from purified human microglia, we observed enrichment for MS genes in these brain-resident immune cells, suggesting that these may have a role in targeting an autoimmune process to the central nervous system, although MS is most likely initially triggered by perturbation of peripheral immune responses.
AB - We analyzed genetic data of 47,429 multiple sclerosis (MS) and 68,374 control subjects and established a reference map of the genetic architecture of MS that includes 200 autosomal susceptibility variants outside the major histocompatibility complex (MHC), one chromosome X variant, and 32 variants within the extended MHC. We used an ensemble of methods to prioritize 551 putative susceptibility genes that implicate multiple innate and adaptive pathways distributed across the cellular components of the immune system. Using expression profiles from purified human microglia, we observed enrichment for MS genes in these brain-resident immune cells, suggesting that these may have a role in targeting an autoimmune process to the central nervous system, although MS is most likely initially triggered by perturbation of peripheral immune responses.
U2 - 10.1126/science.aav7188
DO - 10.1126/science.aav7188
M3 - Journal article
C2 - 31604244
SN - 0036-8075
VL - 365
SP - eaav7188
JO - Science
JF - Science
IS - 6460
ER -