TY - JOUR
T1 - Host single-nucleotide polymorphisms and altered responses to inactivated influenza vaccine
AU - Tang, Yi Wei
AU - Li, Haijing
AU - Wu, Huiyun
AU - Shyr, Yu
AU - Edwards, Kathryn M.
N1 - Funding Information:
Received 29 March 2007; accepted 9 May 2007; electronically published 29 August 2007. Potential conflicts of interest: none reported. Financial support: National Institutes of Health (grants AI-54174 and AI-52594); Connaught. Reprints or correspondence: Dr. Yi-Wei Tang, Molecular Infectious Disease Laboratory, Vanderbilt University Hospital, 4605 TVC, Nashville, TN 37232-5310 (yiwei.tang@ vanderbilt.edu).
PY - 2007
Y1 - 2007
N2 - We analyzed the relationship between host gene polymorphisms and responses in recipients of inactivated influenza vaccine, who were classified into poor, normal, or adverse response groups. The frequency of the mannose-binding lectin-2 codon 54 allele was significantly different among the 3 types of responders, with a decreased odds ratio for the development of poor or adverse responses (P = .033). There was no statistical relationship between responses and either tumor necrosis factor-α or interleukin (IL)-10 promoter polymorphisms among the 3 response groups. When poor and normal responses were combined, the -1082 A allele in the IL-10 promoter conferred a significantly decreased risk of the development of adverse responses (P = .041). These data indicate that host polymorphisms play a role in determining responses to influenza vaccine.
AB - We analyzed the relationship between host gene polymorphisms and responses in recipients of inactivated influenza vaccine, who were classified into poor, normal, or adverse response groups. The frequency of the mannose-binding lectin-2 codon 54 allele was significantly different among the 3 types of responders, with a decreased odds ratio for the development of poor or adverse responses (P = .033). There was no statistical relationship between responses and either tumor necrosis factor-α or interleukin (IL)-10 promoter polymorphisms among the 3 response groups. When poor and normal responses were combined, the -1082 A allele in the IL-10 promoter conferred a significantly decreased risk of the development of adverse responses (P = .041). These data indicate that host polymorphisms play a role in determining responses to influenza vaccine.
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U2 - 10.1086/521370
DO - 10.1086/521370
M3 - Article
C2 - 17763324
AN - SCOPUS:35348870991
SN - 0022-1899
VL - 196
SP - 1021
EP - 1025
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 7
ER -