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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Indoleamine 2,3-dioxygenase is increased in hemodialysis patients and affects immune response to hepatitis B vaccination

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Author
Eleftheriadis, T.; Liakopoulos, V.; Antoniadi, G.; Stefanidis, I.; Galaktidou, G.
Date
2011
DOI
10.1016/j.vaccine.2011.01.051
Keyword
HBV
Vaccine
Indoleamine 2,3-dioxygenase
Hemodialysis
Inflammation
Immune response
STAGE RENAL-DISEASE
CHRONIC INFLAMMATION
ZETA-CHAIN
TRYPTOPHAN
CATABOLITES
ALLOGRAFT-REJECTION
KYNURENINE PATHWAY
QUINOLINIC ACID
EXPRESSION
ACTIVATION
METABOLISM
Immunology
Medicine, Research & Experimental
Metadata display
Abstract
Background: Acquired immunity is impaired in hemodialysis (HD) patients. Indoleamine 2,3-dioxygenase (IDO) is inducible by inflammation and through tryptophan depletion and generation of kynurenine pathway products suppresses adaptive immune response. In the present study plasma IDO levels were assessed in HD patients. Its effect on response to HBV vaccination program was evaluated. Patients and methods: Sixty-six HD patients and twenty-four healthy volunteers enrolled into the study. All the HD patients were initially vaccinated with four double doses of recombinant HBV vaccine. All doses were repeated in patients who had not responded after complete first vaccination series. Only one boost dose was being administered in patients with initial adequate antibody levels against the HBV surface antigen (anti-HBs > 10 IU/L) who then presented with reduced anti-HBs levels. IDO, CRP, IL-6 and TNF-alpha were measured by means of ELISA. Results: Compared to healthy volunteers, IDO levels were twice higher in HD patients. CRP, IL-6 and TNF-alpha were also much higher in HD patients. IDO levels were almost twice higher in HD patients with inadequate response to HBV vaccination, than in those with adequate immune response. CRP, IL-6 and TNF-alpha did not differ between the two patients' groups. IDO was negatively correlated with all markers of inflammation in HD patients. Conclusion: IDO is increased in HD patients. It is possible that after its initial upregulation due to chronic inflammation, IDO curtails its own provoking agent, i.e., inflammation. Increased IDO suppresses adaptive immunity in HD patients, as it is assessed by the response to HBV vaccination. (C) 2011 Elsevier Ltd. All rights reserved.
URI
http://hdl.handle.net/11615/27320
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