Pyogenic bacterial infections in humans with MyD88 deficiency
Date
2008Author
Issekutz, Andrew
Camcioglu, Yildiz
Casanova, Jean-Laurent
Anton, Jordi
Pascal, Mariona
Chang, Huey-Hsuan
Janniere, Lucile
Rose, Yoann
Garty, Ben-Zion
Chapel, Helen
Marodi, Laszlo
Puel, Anne
Chaussabel, Damien
Li, Xiaoxia
Abel, Laurent
Banchereau, Jacques
Rodriguez-Gallego, Carlos
von Bernuth, Horst
Picard, Capucine
Jin, Zhongbo
Pankla, Rungnapa
Xiao, Hui
Ku, Cheng-Lung
Chrabieh, Maya
Ben Mustapha, Imen
Ghandil, Pegah
Vasconcelos, Julia
Sirvent, Nicolas
Guedes, Margarida
Vitor, Artur Bonito
Herrero-Mata, Maria Jose
Arostegui, Juan Ignacio
Rodrigo, Carlos
Alsina, Laia
Ruiz-Ortiz, Estibaliz
Juan, Manel
Fortuny, Claudia
Yague, Jordi
Metadata
Show full item recordAbstract
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.
Collections
- Makale [92796]