Association between common Toll-like receptor 4 mutations and severe respiratory syncytial virus disease
G Tal, A Mandelberg, I Dalal, K Cesar… - The Journal of …, 2004 - academic.oup.com
G Tal, A Mandelberg, I Dalal, K Cesar, E Somekh, A Tal, A Oron, S Itskovich, A Ballin…
The Journal of infectious diseases, 2004•academic.oup.comBackground. The clinical spectrum of respiratory syncytial virus (RSV) bronchiolitis in
previously healthy infants is extremely variable. Thus, it is likely that factors such as genetic
heterogeneity contribute to disease severity. Toll-like receptor 4 (TLR4) and CD14 are part
of a receptor complex involved in the innate immune response to RSV. Methods. The
association of the TLR4 mutations (Asp299Gly and Thr399Ile) and the CD14/− 159
polymorphism were analyzed in 99 infants hospitalized with severe RSV bronchiolitis (group …
previously healthy infants is extremely variable. Thus, it is likely that factors such as genetic
heterogeneity contribute to disease severity. Toll-like receptor 4 (TLR4) and CD14 are part
of a receptor complex involved in the innate immune response to RSV. Methods. The
association of the TLR4 mutations (Asp299Gly and Thr399Ile) and the CD14/− 159
polymorphism were analyzed in 99 infants hospitalized with severe RSV bronchiolitis (group …
Abstract
Background . The clinical spectrum of respiratory syncytial virus (RSV) bronchiolitis in previously healthy infants is extremely variable. Thus, it is likely that factors such as genetic heterogeneity contribute to disease severity. Toll-like receptor 4 (TLR4) and CD14 are part of a receptor complex involved in the innate immune response to RSV.
Methods . The association of the TLR4 mutations (Asp299Gly and Thr399Ile) and the CD14/−159 polymorphism were analyzed in 99 infants hospitalized with severe RSV bronchiolitis (group I). Eighty-two ambulatory infants with mild RSV bronchiolitis (group II) and 90 healthy adults (group III) composed the 2 control groups. The TLR4 mutations and the CD14/−159 polymorphism were genotyped by use of reverse-transcriptase polymerase chain reaction and restriction fragment-length polymorphism analysis, respectively.
Results . Each of the TLR4 mutations, either alone or in cosegregation, were associated with severe RSV bronchiolitis: the Asp299Gly and Thr399Ile mutations were significantly overrepresented in group I, compared with groups II and III. No association between the CD14/−159 polymorphism and RSV bronchiolitis was found.
Conclusions . These findings suggest that TLR4 mutations, but not the CD14/−159 polymorphism, are associated with an increased risk of severe RSV bronchiolitis in previously healthy infants.
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