TY - JOUR
T1 - Unravelling the Connection Between Energy Metabolism and Immune Senescence/Exhaustion in Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
AU - Campenhout, Jente Van
AU - Buntinx, Yanthe
AU - Xiong, Huan-Yu
AU - Wyns, Arne
AU - Polli, Andrea
AU - Nijs, Jo
AU - Aerts, Joeri L.
AU - Laeremans, Thessa
AU - Hendrix, Jolien
N1 - Funding Information:
This research was supported by ME Research UK (SCIO charity number SCO36942) and by Fonds Wetenschappelijk Onderzoek, grant number FWOTM1249, FWOTM1051 and FWOTM1069, which are a PhD fellowship of Huan-Yu Xiong, a senior post-doctoral fellowship of Andrea Polli, and a PhD fellowship of Jolien Hendrix.
Publisher Copyright:
© 2025 by the authors.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a debilitating disease, characterized by a diverse array of symptoms including post-exertional malaise (PEM), severe fatigue, and cognitive impairments, all of which drastically diminish the patients’ quality of life. Despite its impact, no curative treatments exist, largely due to the limited understanding of the disease’s underlying pathophysiology. Mitochondrial dysfunction, leading to impaired energy production and utilization, is believed to play a key role in the onset of fatigue and PEM, positioning it as a potential key pathophysiological mechanism underlying ME/CFS. Additionally, the disorder shows similarities to chronic viral infections, with frequent reports of immune system alterations, suggesting a critical role for immune (dys)functioning. In particular, the roles of immune senescence and immune exhaustion—two fundamental immune states—remain poorly understood in ME/CFS. This state-of-the-art review explores how metabolic dysfunction and immune dysfunction may be interconnected in ME/CFS, proposing that energy deficits may directly impair immune function. By examining this metabolic–immune interplay, this review highlights potential pathways for developing innovative therapeutic strategies that target both energy metabolism and immune regulation, offering hope for improving patient outcomes.
AB - Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a debilitating disease, characterized by a diverse array of symptoms including post-exertional malaise (PEM), severe fatigue, and cognitive impairments, all of which drastically diminish the patients’ quality of life. Despite its impact, no curative treatments exist, largely due to the limited understanding of the disease’s underlying pathophysiology. Mitochondrial dysfunction, leading to impaired energy production and utilization, is believed to play a key role in the onset of fatigue and PEM, positioning it as a potential key pathophysiological mechanism underlying ME/CFS. Additionally, the disorder shows similarities to chronic viral infections, with frequent reports of immune system alterations, suggesting a critical role for immune (dys)functioning. In particular, the roles of immune senescence and immune exhaustion—two fundamental immune states—remain poorly understood in ME/CFS. This state-of-the-art review explores how metabolic dysfunction and immune dysfunction may be interconnected in ME/CFS, proposing that energy deficits may directly impair immune function. By examining this metabolic–immune interplay, this review highlights potential pathways for developing innovative therapeutic strategies that target both energy metabolism and immune regulation, offering hope for improving patient outcomes.
KW - mitochondrial dysfunction
KW - biomarker
KW - natural killer cell
KW - cytotoxic T cell
KW - FATIGUE
KW - pain
UR - https://doi.org/10.3390/biom15030357
UR - http://www.scopus.com/inward/record.url?scp=105001406842&partnerID=8YFLogxK
U2 - 10.3390/biom15030357
DO - 10.3390/biom15030357
M3 - Article
C2 - 40149893
SN - 2218-273X
VL - 15
SP - 1
EP - 22
JO - Biomolecules
JF - Biomolecules
IS - 3
M1 - 357
ER -