Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients.

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Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients. / Kaufmann, Ines; Eisner, Christoph; Richter, Hans Peter; Huge, Volker; Beyer, Antje; Chouker, Alexander; Schelling, Gustav; Thiel, Manfred.

In: NEUROIMMUNOMODULAT, Vol. 14, No. 5, 5, 2007, p. 272-280.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Kaufmann, I, Eisner, C, Richter, HP, Huge, V, Beyer, A, Chouker, A, Schelling, G & Thiel, M 2007, 'Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients.', NEUROIMMUNOMODULAT, vol. 14, no. 5, 5, pp. 272-280. <http://www.ncbi.nlm.nih.gov/pubmed/18239379?dopt=Citation>

APA

Kaufmann, I., Eisner, C., Richter, H. P., Huge, V., Beyer, A., Chouker, A., Schelling, G., & Thiel, M. (2007). Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients. NEUROIMMUNOMODULAT, 14(5), 272-280. [5]. http://www.ncbi.nlm.nih.gov/pubmed/18239379?dopt=Citation

Vancouver

Kaufmann I, Eisner C, Richter HP, Huge V, Beyer A, Chouker A et al. Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients. NEUROIMMUNOMODULAT. 2007;14(5):272-280. 5.

Bibtex

@article{05e3687daaa64b6d8d90a3417c737173,
title = "Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients.",
abstract = "BACKGROUND: The complex regional pain syndrome (CRPS) and fibromyalgia (FM) are chronic pain syndromes occurring in highly stressed individuals. Despite the known connection between the nervous system and immune cells, information on distribution of lymphocyte subsets under stress and pain conditions is limited. METHODS: We performed a comparative study in 15 patients with CRPS type I, 22 patients with FM and 37 age- and sex-matched healthy controls and investigated the influence of pain and stress on lymphocyte number, subpopulations and the Th1/Th2 cytokine ratio in T lymphocytes. RESULTS: Lymphocyte numbers did not differ between groups. Quantitative analyses of lymphocyte subpopulations showed a significant reduction of cytotoxic CD8+ lymphocytes in both CRPS (p <0.01) and FM (p <0.05) patients as compared with healthy controls. Additionally, CRPS patients were characterized by a lower percentage of IL-2-producing T cell subpopulations reflecting a diminished Th1 response in contrast to no changes in the Th2 cytokine profile. CONCLUSIONS: Future studies are warranted to answer whether such immunological changes play a pathogenetic role in CRPS and FM or merely reflect the consequences of a pain-induced neurohumoral stress response, and whether they contribute to immunosuppression in stressed chronic pain patients.",
author = "Ines Kaufmann and Christoph Eisner and Richter, {Hans Peter} and Volker Huge and Antje Beyer and Alexander Chouker and Gustav Schelling and Manfred Thiel",
year = "2007",
language = "Deutsch",
volume = "14",
pages = "272--280",
journal = "NEUROIMMUNOMODULAT",
issn = "1021-7401",
publisher = "S. Karger AG",
number = "5",

}

RIS

TY - JOUR

T1 - Lymphocyte subsets and the role of TH1/TH2 balance in stressed chronic pain patients.

AU - Kaufmann, Ines

AU - Eisner, Christoph

AU - Richter, Hans Peter

AU - Huge, Volker

AU - Beyer, Antje

AU - Chouker, Alexander

AU - Schelling, Gustav

AU - Thiel, Manfred

PY - 2007

Y1 - 2007

N2 - BACKGROUND: The complex regional pain syndrome (CRPS) and fibromyalgia (FM) are chronic pain syndromes occurring in highly stressed individuals. Despite the known connection between the nervous system and immune cells, information on distribution of lymphocyte subsets under stress and pain conditions is limited. METHODS: We performed a comparative study in 15 patients with CRPS type I, 22 patients with FM and 37 age- and sex-matched healthy controls and investigated the influence of pain and stress on lymphocyte number, subpopulations and the Th1/Th2 cytokine ratio in T lymphocytes. RESULTS: Lymphocyte numbers did not differ between groups. Quantitative analyses of lymphocyte subpopulations showed a significant reduction of cytotoxic CD8+ lymphocytes in both CRPS (p <0.01) and FM (p <0.05) patients as compared with healthy controls. Additionally, CRPS patients were characterized by a lower percentage of IL-2-producing T cell subpopulations reflecting a diminished Th1 response in contrast to no changes in the Th2 cytokine profile. CONCLUSIONS: Future studies are warranted to answer whether such immunological changes play a pathogenetic role in CRPS and FM or merely reflect the consequences of a pain-induced neurohumoral stress response, and whether they contribute to immunosuppression in stressed chronic pain patients.

AB - BACKGROUND: The complex regional pain syndrome (CRPS) and fibromyalgia (FM) are chronic pain syndromes occurring in highly stressed individuals. Despite the known connection between the nervous system and immune cells, information on distribution of lymphocyte subsets under stress and pain conditions is limited. METHODS: We performed a comparative study in 15 patients with CRPS type I, 22 patients with FM and 37 age- and sex-matched healthy controls and investigated the influence of pain and stress on lymphocyte number, subpopulations and the Th1/Th2 cytokine ratio in T lymphocytes. RESULTS: Lymphocyte numbers did not differ between groups. Quantitative analyses of lymphocyte subpopulations showed a significant reduction of cytotoxic CD8+ lymphocytes in both CRPS (p <0.01) and FM (p <0.05) patients as compared with healthy controls. Additionally, CRPS patients were characterized by a lower percentage of IL-2-producing T cell subpopulations reflecting a diminished Th1 response in contrast to no changes in the Th2 cytokine profile. CONCLUSIONS: Future studies are warranted to answer whether such immunological changes play a pathogenetic role in CRPS and FM or merely reflect the consequences of a pain-induced neurohumoral stress response, and whether they contribute to immunosuppression in stressed chronic pain patients.

M3 - SCORING: Zeitschriftenaufsatz

VL - 14

SP - 272

EP - 280

JO - NEUROIMMUNOMODULAT

JF - NEUROIMMUNOMODULAT

SN - 1021-7401

IS - 5

M1 - 5

ER -