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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Associations of ABO, D, and Lewis blood groups and HLA Class I and Class II alleles with West Nile virus Lineage 2 disease outcome in Greece, 2010 to 2013

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Συγγραφέας
Politis C., Parara M., Kremastinou J., Hasapopoulou E., Iniotaki A., Siorenta A., Richardson C., Papa A., Kavallierou L., Asariotou M., Katsarou O., Mougiou A., Dadiotis L., Alexandropoulou Z., Megalou A., Magoula E., Papadopoulou M., Pervanidou D., Baka A., Hadjichristodoulou C.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1111/trf.13667
Λέξη-κλειδί
HLA antigen class 1
HLA antigen class 2
HLA C antigen
HLA DQB1 antigen
HLA DRB1 antigen
adult
aged
Article
blood group ABO system
blood group Lewis system
cohort analysis
controlled study
female
gene frequency
Greece
HLA typing
human
major clinical study
male
morbidity
outcome assessment
risk factor
virus infection
West Nile virus
Blackwell Publishing Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
BACKGROUND: West Nile virus (WNV) infection, commonly asymptomatic, may cause mild West Nile fever (WNF) or potentially fatal neuroinvasive disease (WNND). An outbreak of 262 cases of the new Lineage 2 strain in Greece in 2010 continued with high mortality (17%) in WNND. The objective was to investigate ABO, D, and Lewis blood groups, as well as HLA Class I and Class II alleles, in relation to WNV Lineage 2 disease morbidity. STUDY DESIGN AND METHODS: A cohort of 132 Greek WNV cases in 2010 to 2013 (65% male; mean age 64 years; 41% WNF, 59% WNND) was compared to 51,339 healthy WNV-negative blood donors and 246 healthy subjects. RESULTS: Blood group A was more common in WNV cases (51%) than blood donors (39%) and group O less common (32% vs. 42%). D negativity within group A was higher in WNV than in blood donors (18% vs. 10%, p = 0.044). The frequency of secretors (Lewis(a–b+)) was 60% in WNV and 68% in donors (p = 0.16). HLA alleles C*08, DRB1*O4:O5, and DQB1*O2 occurred significantly less frequently in WNV than controls (p < 0.05 unadjusted for multiple testing) and DRB1*10:O1 more frequently (p = 0.039). CONCLUSION: This first study of symptomatic WNV Lineage 2 suggests A/D negativity as a new risk factor associated with WNV infection and level of morbidity. Further studies are required of the possibility that HLA C*08, DRB1*O4:O5, and DQB1*O2 are protective alleles and DRB1*10:O1 a “susceptible” allele to WNV infection and the role of secretor status in relation to WNV infection. © 2016 AABB
URI
http://hdl.handle.net/11615/78293
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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