Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and parallels with autoimmune disorders

Ekua Brenu, Lotti Tajouri, Kevin John Ashton, Donald Staines, Sonya Marshall-Gradisnik

Research output: Chapter in Book/Report/Conference proceedingChapterResearchpeer-review

Abstract

Autoimmune disorders are known to affect a substantial number of people worldwide and in some cases may be fatal. They occur in the presence of unregulated inflammatory responses including failure in self-tolerance. Some unexplained disorders with immune compromises may demonstrate certain characteristics that suggest an autoimmune disorder including Chronic Fatigue syndrome/Myalgic Encephalomyelitis (CFS/ME). CFS/ME remains an unsolved disorder with multiple symptoms and no single causative factor. These symptoms may include but are not limited to incapacitating fatigue, weakened short term memory or attentiveness, sore throat, tender cervical or axillary lymph nodes, muscle pain, severe headaches, impaired sleep and postexertional malaise. To date succinct and concise mechanisms that underlie this disorder have not yet being identified although, many hypotheses have been put forward. CFS/ME often occurs as a consequence of a post-infectious episode accompanied by compromises in the immune, endocrine and nervous systems. The consequences of these events have not being clearly identified. Importantly, immune deterioration in CFS/ME is related to heightened or suppressed cell function, differential gene expression, equivocal levels of immune cell numbers and protein secretion promoting adverse inflammatory activation. Both innate and adaptive immune system perturbations persist in CFS/ME. These characteristics are in many respects similar to mechanisms of disease in autoimmune disorders suggesting that the changes in immune response may develop from cellular and molecular changes in immune cells and proteins. We propose here that as the mechanism of CFS/ME may involve certain immunological factors that have been shown to be compromised in other autoimmune diseases, CFS/ME may in some cases have an autoimties of neutrophils in MS include heightened levels of IL-8, TLR2, degranulation, impediment in apoptosis (Naegele et al., 2012).
Original languageEnglish
Title of host publicationGenes and Autoimmunity - Intracellular Signaling and Microbiome Contribution
EditorsS A Stanilova
Place of PublicationCroatia
PublisherIn-Tech
Chapter10
Pages205-235
Number of pages31
ISBN (Print)9789535110286
DOIs
Publication statusPublished - 2013

Fingerprint

Chronic Fatigue Syndrome
Autoimmune Diseases
Immune System
Self Tolerance
Endocrine System
Pharyngitis
Myalgia
Immune System Diseases
Immunologic Factors
Interleukin-8
Short-Term Memory
Nervous System
Fatigue
Headache

Cite this

Brenu, E., Tajouri, L., Ashton, K. J., Staines, D., & Marshall-Gradisnik, S. (2013). Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and parallels with autoimmune disorders. In S. A. Stanilova (Ed.), Genes and Autoimmunity - Intracellular Signaling and Microbiome Contribution (pp. 205-235). Croatia : In-Tech. https://doi.org/10.5772/53440
Brenu, Ekua ; Tajouri, Lotti ; Ashton, Kevin John ; Staines, Donald ; Marshall-Gradisnik, Sonya. / Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and parallels with autoimmune disorders. Genes and Autoimmunity - Intracellular Signaling and Microbiome Contribution. editor / S A Stanilova. Croatia : In-Tech, 2013. pp. 205-235
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Brenu, E, Tajouri, L, Ashton, KJ, Staines, D & Marshall-Gradisnik, S 2013, Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and parallels with autoimmune disorders. in SA Stanilova (ed.), Genes and Autoimmunity - Intracellular Signaling and Microbiome Contribution. In-Tech, Croatia , pp. 205-235. https://doi.org/10.5772/53440

Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and parallels with autoimmune disorders. / Brenu, Ekua; Tajouri, Lotti; Ashton, Kevin John; Staines, Donald; Marshall-Gradisnik, Sonya.

Genes and Autoimmunity - Intracellular Signaling and Microbiome Contribution. ed. / S A Stanilova. Croatia : In-Tech, 2013. p. 205-235.

Research output: Chapter in Book/Report/Conference proceedingChapterResearchpeer-review

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PY - 2013

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N2 - Autoimmune disorders are known to affect a substantial number of people worldwide and in some cases may be fatal. They occur in the presence of unregulated inflammatory responses including failure in self-tolerance. Some unexplained disorders with immune compromises may demonstrate certain characteristics that suggest an autoimmune disorder including Chronic Fatigue syndrome/Myalgic Encephalomyelitis (CFS/ME). CFS/ME remains an unsolved disorder with multiple symptoms and no single causative factor. These symptoms may include but are not limited to incapacitating fatigue, weakened short term memory or attentiveness, sore throat, tender cervical or axillary lymph nodes, muscle pain, severe headaches, impaired sleep and postexertional malaise. To date succinct and concise mechanisms that underlie this disorder have not yet being identified although, many hypotheses have been put forward. CFS/ME often occurs as a consequence of a post-infectious episode accompanied by compromises in the immune, endocrine and nervous systems. The consequences of these events have not being clearly identified. Importantly, immune deterioration in CFS/ME is related to heightened or suppressed cell function, differential gene expression, equivocal levels of immune cell numbers and protein secretion promoting adverse inflammatory activation. Both innate and adaptive immune system perturbations persist in CFS/ME. These characteristics are in many respects similar to mechanisms of disease in autoimmune disorders suggesting that the changes in immune response may develop from cellular and molecular changes in immune cells and proteins. We propose here that as the mechanism of CFS/ME may involve certain immunological factors that have been shown to be compromised in other autoimmune diseases, CFS/ME may in some cases have an autoimties of neutrophils in MS include heightened levels of IL-8, TLR2, degranulation, impediment in apoptosis (Naegele et al., 2012).

AB - Autoimmune disorders are known to affect a substantial number of people worldwide and in some cases may be fatal. They occur in the presence of unregulated inflammatory responses including failure in self-tolerance. Some unexplained disorders with immune compromises may demonstrate certain characteristics that suggest an autoimmune disorder including Chronic Fatigue syndrome/Myalgic Encephalomyelitis (CFS/ME). CFS/ME remains an unsolved disorder with multiple symptoms and no single causative factor. These symptoms may include but are not limited to incapacitating fatigue, weakened short term memory or attentiveness, sore throat, tender cervical or axillary lymph nodes, muscle pain, severe headaches, impaired sleep and postexertional malaise. To date succinct and concise mechanisms that underlie this disorder have not yet being identified although, many hypotheses have been put forward. CFS/ME often occurs as a consequence of a post-infectious episode accompanied by compromises in the immune, endocrine and nervous systems. The consequences of these events have not being clearly identified. Importantly, immune deterioration in CFS/ME is related to heightened or suppressed cell function, differential gene expression, equivocal levels of immune cell numbers and protein secretion promoting adverse inflammatory activation. Both innate and adaptive immune system perturbations persist in CFS/ME. These characteristics are in many respects similar to mechanisms of disease in autoimmune disorders suggesting that the changes in immune response may develop from cellular and molecular changes in immune cells and proteins. We propose here that as the mechanism of CFS/ME may involve certain immunological factors that have been shown to be compromised in other autoimmune diseases, CFS/ME may in some cases have an autoimties of neutrophils in MS include heightened levels of IL-8, TLR2, degranulation, impediment in apoptosis (Naegele et al., 2012).

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M3 - Chapter

SN - 9789535110286

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EP - 235

BT - Genes and Autoimmunity - Intracellular Signaling and Microbiome Contribution

A2 - Stanilova, S A

PB - In-Tech

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ER -

Brenu E, Tajouri L, Ashton KJ, Staines D, Marshall-Gradisnik S. Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and parallels with autoimmune disorders. In Stanilova SA, editor, Genes and Autoimmunity - Intracellular Signaling and Microbiome Contribution. Croatia : In-Tech. 2013. p. 205-235 https://doi.org/10.5772/53440