https://journals.sagepub.com/doi/10.1177/2058738418820402
It is getting more interesting! I could be wrong, but I think I am starting to see some dots connected in ME/CFS with this article.
To the best of our knowledge, this is the first RNA-seq that has analysed PBMCs of ME/CFS patients. This technology was, however, used in a recent whole blood study analysing adolescent ME/CFS participants by gene set enrichment.4 Our analysis was consistent with their findings, suggesting impairment of B cell differentiation and survival, enhanced innate antiviral responses and inflammation. Co-expression patterns and single gene transcripts were associated with neuroendocrine markers of altered HPA axis and autonomic nervous activity, plasma cortisol, blood monocyte and eosinophil counts. We have found significant molecular changes in our ME/CFS cohort that are consistent with those reported in larger complementary but not identical studies. Previous microarray and differential display studies of gene expression in ME/CFS have indicated disturbances in immune pathways, mitochondrial function, cell stress and apoptosis.
It is getting more interesting! I could be wrong, but I think I am starting to see some dots connected in ME/CFS with this article.
To the best of our knowledge, this is the first RNA-seq that has analysed PBMCs of ME/CFS patients. This technology was, however, used in a recent whole blood study analysing adolescent ME/CFS participants by gene set enrichment.4 Our analysis was consistent with their findings, suggesting impairment of B cell differentiation and survival, enhanced innate antiviral responses and inflammation. Co-expression patterns and single gene transcripts were associated with neuroendocrine markers of altered HPA axis and autonomic nervous activity, plasma cortisol, blood monocyte and eosinophil counts. We have found significant molecular changes in our ME/CFS cohort that are consistent with those reported in larger complementary but not identical studies. Previous microarray and differential display studies of gene expression in ME/CFS have indicated disturbances in immune pathways, mitochondrial function, cell stress and apoptosis.
Last edited: