Comparable Immune Alterations and Inflammatory Signatures in ME/CFS and Long COVID

<b>Background:</b> Chronic Fatigue Syndrome (CFS), also known as Myalgic Encephalomyelitis (ME), is a debilitating condition characterized by persistent fatigue and multisystemic symptoms, such as cognitive impairment, musculoskeletal pain, and post-exertional malaise. Recently, parallels have been drawn between ME/CFS and Long COVID, a post-viral syndrome following infection with SARS-CoV-2, which shares many clinical features with CFS. Both conditions involve chronic immune activation, raising questions about their immunopathological overlap. <b>Objectives:</b> This study aimed to compare immune biomarkers between patients with ME/CFS or Long COVID and healthy controls to explore shared immune dysfunction. <b>Methods:</b> We analyzed lymphocyte subsets, cytokine profiles, psychological status and their correlations in 190 participants, 65 with CFS, 54 with Long COVID, and 70 healthy controls. <b>Results:</b> When compared to healthy subjects, results in both conditions were marked by lower levels of lymphocytes (CFS-2.472 × 10<sup>9</sup>/L, <i>p</i> = 0.006, LC-2.051 × 10<sup>9</sup>/L, <i>p</i> = 0.009), CD8<sup>+</sup> T cells (CFS-0.394 × 10<sup>9</sup>/L, <i>p</i> = 0.001, LC-0.404 × 10<sup>9</sup>/L, <i>p</i> = 0.001), and NK cells (CFS-0.205 × 10<sup>9</sup>/L, <i>p</i> = 0.001, LC-0.180 × 10<sup>9</sup>/L, <i>p</i> = 0.001), and higher levels of proinflammatory cytokines such as IL-6 (CFS-3.35 pg/mL, <i>p</i> = 0.050 LC-4.04 pg/mL, <i>p</i> = 0.001), TNF (CFS-2.64 pg/mL, <i>p</i> = 0.023, LC-2.50 pg/mL, <i>p</i> = 0.025), IL-4 (CFS-3.72 pg/mL, <i>p</i> = 0.041, LC-3.45 pg/mL, <i>p</i> = 0.048), and IL-10 (CFS-2.29 pg/mL, <i>p</i> = 0.039, LC-2.25 pg/mL, <i>p</i> = 0.018). <b>Conclusions:</b> Notably, there were no significant differences between CFS and Long COVID patients in the tested biomarkers. These results demonstrate that ME/CFS and Long COVID display comparable immune and inflammatory profiles, with no significant biomarker differences observed between the two groups.

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Journal
Biomedicines
Published
2025-12-08
DOI
https://doi.org/10.3390/biomedicines13123001
Primary Topic
Fibromyalgia and Chronic Fatigue Syndrome Research
Type
article
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article

Comparable Immune Alterations and Inflammatory Signatures in ME/CFS and Long COVID

Mariya Ivanovska, С. В. Петров, Marianna Murdjeva, Yana Todorova et al.
Biomedicines
Fibromyalgia and Chronic Fatigue Syndrome Research
article

Comparable Immune Alterations and Inflammatory Signatures in ME/CFS and Long COVID

Mariya Ivanovska, С. В. Петров, Marianna Murdjeva, Yana Todorova, Ralitsa Nikolova, Milena Aleksova, Teodora Kalfova, Martina Bozhkova, Hristo Taskov, Maria Nikolova, Michael Maes, Dobrina Dudova, Katya Vaseva
article en

Abstract

<b>Background:</b> Chronic Fatigue Syndrome (CFS), also known as Myalgic Encephalomyelitis (ME), is a debilitating condition characterized by persistent fatigue and multisystemic symptoms, such as cognitive impairment, musculoskeletal pain, and post-exertional malaise. Recently, parallels have been drawn between ME/CFS and Long COVID, a post-viral syndrome following infection with SARS-CoV-2, which shares many clinical features with CFS. Both conditions involve chronic immune activation, raising questions about their immunopathological overlap. <b>Objectives:</b> This study aimed to compare immune biomarkers between patients with ME/CFS or Long COVID and healthy controls to explore shared immune dysfunction. <b>Methods:</b> We analyzed lymphocyte subsets, cytokine profiles, psychological status and their correlations in 190 participants, 65 with CFS, 54 with Long COVID, and 70 healthy controls. <b>Results:</b> When compared to healthy subjects, results in both conditions were marked by lower levels of lymphocytes (CFS-2.472 × 10<sup>9</sup>/L, <i>p</i> = 0.006, LC-2.051 × 10<sup>9</sup>/L, <i>p</i> = 0.009), CD8<sup>+</sup> T cells (CFS-0.394 × 10<sup>9</sup>/L, <i>p</i> = 0.001, LC-0.404 × 10<sup>9</sup>/L, <i>p</i> = 0.001), and NK cells (CFS-0.205 × 10<sup>9</sup>/L, <i>p</i> = 0.001, LC-0.180 × 10<sup>9</sup>/L, <i>p</i> = 0.001), and higher levels of proinflammatory cytokines such as IL-6 (CFS-3.35 pg/mL, <i>p</i> = 0.050 LC-4.04 pg/mL, <i>p</i> = 0.001), TNF (CFS-2.64 pg/mL, <i>p</i> = 0.023, LC-2.50 pg/mL, <i>p</i> = 0.025), IL-4 (CFS-3.72 pg/mL, <i>p</i> = 0.041, LC-3.45 pg/mL, <i>p</i> = 0.048), and IL-10 (CFS-2.29 pg/mL, <i>p</i> = 0.039, LC-2.25 pg/mL, <i>p</i> = 0.018). <b>Conclusions:</b> Notably, there were no significant differences between CFS and Long COVID patients in the tested biomarkers. These results demonstrate that ME/CFS and Long COVID display comparable immune and inflammatory profiles, with no significant biomarker differences observed between the two groups.

BiomedicinesVol. 13(12)
University of Electronic Science and Technology of China (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Medical University Plovdiv (BG), University of Telecommunications and Post (BG), National Center of Infectious and Parasitic Diseases (BG), Medical University Pleven (BG)
Openalex Percentile: Top 54%
Fibromyalgia and Chronic Fatigue Syndrome Research
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