Studies that explore the role of adaptive immunity and NcP
Study and reference | Mechanism involved | NcP condition |
---|---|---|
T helper involvement | ||
Guggino et al. [65] | Th activation with an increase of a pro-inflammatory state, in particular by TNF-alpha | FM patients |
Dolcino et al. [66] | Th17 polarization, associated with higher levels of CD4+ T cells and of sTGF-beta, IL 6, IL 21 | FM patients |
Koike et al. [68] | High CD4/CD8 ratio identified as an independent variable for pain development | Burning mouth syndrome patients |
Quick et al. [69] | T helper polarization with increased expression of interferon-gamma and IL 17A | Mouse model of pelvic pain |
Chen et al. [70] | Th1, Th17, and Th22 cells increase in the peripheral blood with augmented pro-inflammatory state | Male patient with pelvic pain |
Lenert et al. [73] | Reduction of peripheral Th2-cells that was linked to sustained inflammation | Mice model of chronic muscle pain |
Chen et al. [74] | Th1 hyper-expression that supports persisting inflammation with increased levels of interferon-gamma associated with reduced IL 10 | IBS patients |
B cell involvement | ||
Fineschi et al. [76] | Elevated B cell levels and a heightened interferon-pro-inflammatory signature | FM patients |
Goebel et al. [77] | IgG against satellite glial cells, neurons, myelin fibers, macrophages, and endothelial cells induces sensory hypersensitivity | Mouse model of FM |
Ryabkova et al. [80] | Autoantibodies against collagen, gastric, pulmonary cells, and beta 2 glycoprotein | Chronic fatigue syndrome patients |
Cuhadar et al. [81] | Pathological auto-IgG transferring enhances hyperalgesia | Mouse model of CRPS |
Ohman et al. [82] | Augmented expression of B cells, IgG, and the co-stimulatory molecules CD80 and CD86 | IBS patients |
Dunphy [83] | Auto-IgG against nucleolar autoantigen | Pelvic pain patients |
NcP: nociplastic pain; Th: T helper cells; TNF: tumor necrosis factor; FM: fibromyalgia; IL: interleukin; IgG: immunoglobulin G; CRPS: complex regional pain syndrome; IBS: irritable bowel syndrome
MG and AC: Conceptualization, Investigation, Writing—original draft, Writing—review & editing. AP: Investigation, Writing—original draft, Writing—review & editing. FP: Conceptualization, Validation, Writing—review & editing, Supervision. GV: Validation, Writing—review & editing, Supervision. All authors read and approved the submitted version.
Giustino Varrassi, the Editorial Board Member and a Guest Editor of Exploration of Immunology, had no involvement in the decision-making or the review process of this manuscript. The other authors declare no conflicts of interest.
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