Succumbing to the laws of attraction: Exploring the sometimes pathogenic versatility of discrete immune logic
Abstract
Feedback mechanisms throughout the immune and endocrine systems play a significant role in maintaining physiological homeostasis. Specifically, the hypothalamic-pituitary-adrenal (HPA) and hypothalamic-pituitary-gonadal (HPG) axes contribute important oversight of immune activity and homeostatic regulation. We propose that these components form an overarching regulatory system capable of supporting multiple homeostatic regimes. These emerge as a result of the extensive feedback mechanisms involving cytokine and hormone signaling. Here we explore the possible role of such alternate regulatory programs in perpetuating chronic immune and endocrine dysfunction in males. To do this we represent documented interactions within and between components of the male HPA-HPG-immune system as a set of discrete logic circuits. Analysis of these regulatory circuits indicated that even in the absence of external perturbations this model HPA-HPG-immune network supported three distinct and stable homeostatic regimes. To investigate the relevance of these predicted homeostatic regimes, we compared them to experimental data from male subjects with Gulf War illness (GWI) and chronic fatigue syndrome (CFS), two complex chronic conditions presenting with endocrine and immune dysregulation. Results indicated that molecular profiles observed experimentally in male GWI and CFS were both distinct from the normal resting state. Profile alignments suggests that regulatory circuitry is largely intact in male GWI and that the persistent immune dysfunction in this illness may at least in part be facilitated by the body’s own homeostatic drive. Conversely the profile for male CFS was distant from all three stable states suggesting the continued influence of an exogenous agent or lasting changes to the regulatory circuitry such as epigenetic alterations.
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The authors found that even their coarse-grained model could support multiple steady states, two of which were proximal to immune marker profiles exhibited by ME/CFS subjects.
“We found that even this coarse-grained model could support multiple steady states, two of which were proximal to immune marker profiles exhibited by ME/CFS subjects26,27.”
From Leveraging Prior Knowledge of Endocrine Immune Regulation in the Therapeutically-relevant Phenotyping of Women with Chronic Fatigue Syndrome (2019) · cites this paper as [26]
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References 97 · Cited by 16
- Authors
- Fritsch, P., Craddock, T. J., del Rosario, R. M., Rice, M. A., Smylie, A., Folcik, V. A., de Vries, G., Fletcher, M. A., Klimas, N. G., & Broderick, G.
- Affiliations
- University of Alberta (CA)
- Nova Southeastern University (US)
- The Ohio State University (US)
- Corresponding author
- Craddock, Travis JA
- Venue
- Systems Biomedicine
- Publisher
- Informa UK Limited
- Published
- 2013-07
- Volume
- 1
- Issue
- 3
- Pages
- 179-194
- ISSN
- 2162-8130 (ISSN-L)
- 2162-8149
- OpenAlex
- W2594859271
- Cited by
- 16
- References
- 97
- Citations by year
- 2024: 1 · 2023: 1 · 2021: 1 · 2020: 3 · 2019: 2 · 2018: 4 · 2015: 3 · 2014: 1
- FWCI
- 0.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Systems Biomedicine (publishedVersion)
- Funders
- U.S. Department of Defense
- National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Health Sciences › Medicine › Psychiatry and Mental health › Fibromyalgia and Chronic Fatigue Syndrome Research
- Keywords
- hypothalamic-pituitary-adrenal axis, hypothalamic-pituitary-gonadal axis, endocrine-immune interaction, logic circuits, cytokine signaling, hormone signaling, Gulf War illness, chronic fatigue syndrome, immune dysregulation, endocrine dysfunction, epigenetic modifications, male patients
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