A Toll‐like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease

Summary Despite adequate immunization and penicillin prophylaxis, bacterial infections remain a leading cause of morbidity and mortality in patients with sickle cell disease (SCD). Besides hyposplenism, inflammatory and genetic factors might modulate their susceptibility to bacterial infections. We...

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Veröffentlicht in:British journal of haematology 2019-06, Vol.185 (5), p.918-924
Hauptverfasser: Tozatto‐Maio, Karina, Girot, Robert, Ly, Indou D., Rocha, Vanderson, Silva Pinto, Ana C., Diagne, Ibrahima, Benzerara, Yahia, Dinardo, Carla L., Kashima, Simone, Leston‐Araujo, Itauá, Kenzey, Chantal, Fonseca, Guilherme H. H., Rodrigues, Evandra S., Volt, Fernanda, Jarduli, Luciana R., Ruggeri, Annalisa, Mariaselvam, Christina M., Gualandro, Sandra F. M., Elayoubi, Hanadi, Cunha, Renato, Cappelli, Barbara, Malmegrim, Kelen C. R., Simões, Belinda P., Gluckman, Eliane, Tamouza, Ryad
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Sprache:eng
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Zusammenfassung:Summary Despite adequate immunization and penicillin prophylaxis, bacterial infections remain a leading cause of morbidity and mortality in patients with sickle cell disease (SCD). Besides hyposplenism, inflammatory and genetic factors might modulate their susceptibility to bacterial infections. We performed a candidate gene association of single nucleotide polymorphisms (SNPs) located in Toll‐like receptor (TLR) genes, encoding prominent molecules for innate immune responses, with the occurrence of bacterial infections in patients with SCD. A cohort followed in centres in Brazil, France and Senegal (n = 430) was divided in two groups: patients who presented at least one episode of bacterial infection (n = 235) and patients who never had bacterial infections (n = 195). There were no differences in gender or age distribution among the groups. The frequency of the TLR2 rs4696480 TA genotype was significantly lower in the infected group (50% vs. 67%, odds ratio [OR] = 0·50, 95% confidence interval [CI] 0·34–0·75, P 
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.15875