Association of severe respiratory syncytial virus bronchiolitis with interleukin-4 and interleukin-4 receptor α polymorphisms

被引:154
作者
Hoebee, B
Rietveld, E
Bont, L
van Oosten, M
Hodemaekers, HM
Nagelkerke, NJD
Neijens, HJ
Kimpen, JLL
Kimman, TG
机构
[1] Natl Inst Publ Hlth & Environm, Hlth Effects Res Lab, NL-3720 BA Bilthoven, Netherlands
[2] Natl Inst Publ Hlth & Environm, Res Lab Infect Dis, NL-3720 BA Bilthoven, Netherlands
[3] Natl Inst Publ Hlth & Environm, Computerizat & Methodol Consultancy Unit, NL-3720 BA Bilthoven, Netherlands
[4] Univ Med Ctr Utrecht, Wilhelmina Childresn Hosp, Utrecht, Netherlands
[5] Sophia Childrens Univ Hosp, Erasmus MC, Dept Pediat, Rotterdam, Netherlands
关键词
D O I
10.1086/345859
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The association of variants of genes encoding interleukin (IL)-4 and the IL-4 receptor alpha chain (IL-4Ralpha) with respiratory syncytial virus (RSV) bronchiolitis was examined in hospitalized infants. Polymorphisms in IL-4 (C-590T) and IL-4Ralpha (I50V and Q551R) were genotyped by restriction fragment-length polymorphism analysis. Control subjects included parents of the hospitalized children (for the transmission/ disequilibrium test), and a random population sample (for the case-control study). Results were also analyzed in a combination of these 2 tests, using Fisher's method. The IL-4 590T allele was found more frequently among children hospitalized with RSV than expected in the case-control (odds ratio [OR], 1.43; P = .04) and combination (OR, 1.41; P = .02) tests. Among children who were >6 months old when they were hospitalized, compared with the control group or with the <6 months old who were hospitalized for RSV infection, higher frequencies of both the IL-4 590T allele and the IL-4R alpha R551 allele were found. These results indicate that gain-of-function variants of T helper type 2 cytokine genes may play a role in increasing the severity of RSV disease, which appears more pronounced after the first half-year of life.
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页码:2 / 11
页数:10
相关论文
共 91 条
[41]   RESPIRATORY SYNCYTIAL VIRUS DISEASE IN INFANTS DESPITE PRIOR ADMINISTRATION OF ANTIGENIC INACTIVATED VACCINE [J].
KIM, HW ;
CANCHOLA, JG ;
BRANDT, CD ;
PYLES, G ;
CHANOCK, RM ;
JENSEN, K ;
PARROTT, RH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1969, 89 (04) :422-+
[42]   SHARING OF THE IL-2 RECEPTOR-GAMMA CHAIN WITH THE FUNCTIONAL IL-9 RECEPTOR COMPLEX [J].
KIMURA, Y ;
TAKESHITA, T ;
KONDO, M ;
ISHII, N ;
NAKAMURA, M ;
VANSNICK, J ;
SUGAMURA, K .
INTERNATIONAL IMMUNOLOGY, 1995, 7 (01) :115-120
[43]   An IL-13 promoter polymorphism associated with increased risk of allergic asthma [J].
Kraan, TCTMV ;
van Veen, A ;
Boeije, LCM ;
van Tuyl, SAP ;
de Groot, ER ;
Stapel, SO ;
Bakker, A ;
Verweij, CL ;
Aarden, LA ;
van der Zee, JS .
GENES AND IMMUNITY, 1999, 1 (01) :61-65
[44]  
Kruse S, 1999, IMMUNOLOGY, V96, P365
[45]   Association between surfactant protein A gene locus and severe respiratory syncytial virus infection in infants [J].
Löfgren, J ;
Rämet, M ;
Renko, M ;
Marttila, R ;
Hallman, M .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (03) :283-289
[46]   Respiratory syncytial virus predisposes mice to augmented allergic airway responses via IL-13-mediated mechanisms [J].
Lukacs, NW ;
Tekkanat, KK ;
Berlin, A ;
Hogaboam, CM ;
Miller, A ;
Evanoff, H ;
Lincoln, P ;
Maassab, H .
JOURNAL OF IMMUNOLOGY, 2001, 167 (02) :1060-1065
[47]   RESPIRATORY SYNCYTIAL VIRAL-INFECTION IN INFANTS WITH CONGENITAL HEART-DISEASE [J].
MACDONALD, NE ;
HALL, CB ;
SUFFIN, SC ;
ALEXSON, C ;
HARRIS, PJ ;
MANNING, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (07) :397-400
[48]   LINKAGE ANALYSIS OF IL4 AND OTHER CHROMOSOME 5Q31.1 MARKERS AND TOTAL SERUM IMMUNOGLOBULIN-E CONCENTRATIONS [J].
MARSH, DG ;
NEELY, JD ;
BREAZEALE, DR ;
GHOSH, B ;
FREIDHOFF, LR ;
EHRLICHKAUTZKY, E ;
SCHOU, C ;
KRISHNASWAMY, G ;
BEATY, TH .
SCIENCE, 1994, 264 (5162) :1152-1156
[49]  
MEULENBELT I, 1995, AM J HUM GENET, V57, P1252
[50]   Ile50Val variant of IL4Rα upregulates IgE synthesis and associates with atopic asthma [J].
Mitsuyasu, H ;
Izuhara, K ;
Mao, XQ ;
Gao, PS ;
Arinobu, Y ;
Enomoto, T ;
Kawai, M ;
Sasaki, S ;
Dake, Y ;
Hamasaki, N ;
Shirakawa, T ;
Hopkin, JM .
NATURE GENETICS, 1998, 19 (02) :119-120