Abstract
Post-acute SarS-Cov2 (PASC), Myalgia encephalomyelitis/Chronic fatigue syndrome (ME/CFS) and Post-acute infection syndrome (PAIS) consist of chronic post–acute infectious syndromes, sharing exhaustive fatigue, post exertional malaise, intermittent pain, postural tachycardia and neuro-cognitive-psychiatric dysfunction. However, the concerned shared pathophysiology is still unresolved in terms of upstream drivers and transducers. Also, risk factors which may determine vulnerability/progression to the chronic phase still remain to be defined. In lack of drivers and a cohesive pathophysiology, the concerned syndromes still remain unmet therapeutic needs. ‘mTORC1 Syndrome’ (TorS) implies an exhaustive disease entity driven by sustained hyper-activation of the mammalian target of rapamycin C1 (mTORC1), and resulting in a variety of disease aspects of the Metabolic Syndrome (MetS), non-alcoholic fatty liver disease, chronic obstructive pulmonary disease, some cancers, neurodegeneration and other [Bar-Tana in Trends Endocrinol Metab 34:135–145, 2023]. TorS may offer a cohesive insight of PASC, ME/CFS and PAIS drivers, pathophysiology, vulnerability and treatment options.
Original language | English |
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Article number | 297 |
Journal | Journal of Translational Medicine |
Volume | 23 |
Issue number | 1 |
DOIs | |
State | Published - Dec 2025 |
Bibliographical note
Publisher Copyright:© The Author(s) 2025.
Keywords
- Mammalian target of rapamycin C1 (mTORC1)
- Myalgia encephalomyelitis/chronic fatigue syndrome (ME/CFS)
- Post-acute SarS-Cov2 (PASC)
- Post-acute infection syndrome (PAIS)
- mTORC1 syndrome (TorS)