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Pyogenic bacterial infections in humans with MyD88 deficiency
Authors:von Bernuth Horst  Picard Capucine  Jin Zhongbo  Pankla Rungnapa  Xiao Hui  Ku Cheng-Lung  Chrabieh Maya  Mustapha Imen Ben  Ghandil Pegah  Camcioglu Yildiz  Vasconcelos Júlia  Sirvent Nicolas  Guedes Margarida  Vitor Artur Bonito  Herrero-Mata María José  Aróstegui Juan Ignacio  Rodrigo Carlos  Alsina Laia  Ruiz-Ortiz Estibaliz  Juan Manel  Fortuny Claudia  Yagüe Jordi  Antón Jordi  Pascal Mariona  Chang Huey-Hsuan  Janniere Lucile  Rose Yoann  Garty Ben-Zion  Chapel Helen  Issekutz Andrew  Maródi László  Rodriguez-Gallego Carlos  Banchereau Jacques  Abel Laurent  Li Xiaoxia  Chaussabel Damien  Puel Anne  Casanova Jean-Laurent
Institution:Human Genetics of Infectious Diseases, INSERM U550, Paris, France.
Abstract:MyD88 is a key downstream adapter for most Toll-like receptors (TLRs) and interleukin-1 receptors (IL-1Rs). MyD88 deficiency in mice leads to susceptibility to a broad range of pathogens in experimental settings of infection. We describe a distinct situation in a natural setting of human infection. Nine children with autosomal recessive MyD88 deficiency suffered from life-threatening, often recurrent pyogenic bacterial infections, including invasive pneumococcal disease. However, these patients were otherwise healthy, with normal resistance to other microbes. Their clinical status improved with age, but not due to any cellular leakiness in MyD88 deficiency. The MyD88-dependent TLRs and IL-1Rs are therefore essential for protective immunity to a small number of pyogenic bacteria, but redundant for host defense to most natural infections.
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