Journal article
The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis
KS Gandhi, FC McKay, M Cox, C Riveros, N Armstrong, RN Heard, S Vucic, DW Williams, J Stankovich, M Brown, P Danoy, GJ Stewart, S Broadley, P Moscato, J Lechner-Scott, RJ Scott, DR Booth
Human Molecular Genetics | Published : 2010
DOI: 10.1093/hmg/ddq090
Abstract
Multiple sclerosis (MS) is an autoimmune disease with a genetic component, caused at least in part by aberrant lymphocyte activity. The whole blood mRNA transcriptome was measured for 99 untreated MS patients: 43 primary progressive MS, 20 secondary progressive MS, 36 relapsing remitting MS and 45 age-matched healthy controls. The ANZgene Multiple Sclerosis Genetics Consortium genotyped more than 300 000 SNPs for 115 of these samples. Transcription from genes on translational regulation, oxidative phosphorylation, immune synapse and antigen presentation pathways was markedly increased in all forms of MS. Expression of genes tagging T cells was also upregulated (P < 10-12) in MS. A T cell gen..
View full abstractGrants
Awarded by Australian Research Council
Funding Acknowledgements
This work was supported by Multiple Sclerosis Research Australia and the Australian Research Council under the Linkage Projects Scheme (LP0776744). K. S. G. is supported by an Australia Research Council Biogen Idec PhD award, M. B. C. is supported by a grant from the John Hunter Hospital Charitable Trust Fund and a special grant from Macquarie Bank.