T cell immunomodulation by bile acid metabolites, 2020, Giovannini et al

Andy

Senior Member (Voting rights)
A short review/opinion piece.
The historical T cell dichotomy (TH1 versus TH2) changed by the identification of TH17 and Treg cells. These populations were linked to a wide range of immunological disorders such as immunodeficiencies, inflammatory and allergic diseases. Subsequently, this dualistic view of T cell biology was overcome by the previously unappreciated plasticity of T cells.

Primary bile acids (BA) are liver-derived steroid acids involved in lipid digestion. Then, colonic bacteria yield secondary BA, which are potentially cytotoxic and carcinogenic. Interestingly, BA have emerged as modulators of innate immunity and gut inflammation. Indeed, there is the notion that molecules containing a sterol-like core act as specific lymphocyte transcriptional factor inhibitors.
Paywall, https://onlinelibrary.wiley.com/doi/pdf/10.1111/all.14223
Sci hub, https://sci-hub.se/10.1111/all.14223

@mariovitali , another one that will probably interest you. :)
 
Thank you for the mention @Andy and @Amw66.

I do know that Derya Unutmaz was supposed to be looking more into Bile acids. He is usually responsive and so i will try to find out whether he thinks that Bile acids metabolism deserves more attention given their importance to TRegs and TH17.

I fear however that the observed disruption of TRegs and TH17 is very likely to be non-ME specific. I feel that we need to check whether TH17/Tregs findings differentiate ME patients from other patients with autoimmune disorders (e.g colitis, psoriasis, RA) :


https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877591/
 
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