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Brain Advance Access originally published online on April 28, 2004
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Brain, Vol. 127, No. 6, 1437-1445, 2004
© 2004 Guarantors of Brain
doi: 10.1093/brain/awh171

MyD88 is required for mounting a robust host immune response to Streptococcus pneumoniae in the CNS

Uwe Koedel1, Tobias Rupprecht1, Barbara Angele1, Juergen Heesemann2, Hermann Wagner3, Hans-Walter Pfister1 and Carsten J. Kirschning3

1 Department of Neurology, Klinikum Grosshadern, 2 Max von Pettenkofer Institute for Hygiene and Microbiology, Ludwig Maximilians University and 3 Institute of Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany

Correspondence to: Professor Hans-Walter Pfister, Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians-University, Marchioninistrasse 15, D-81377 Munich, Germany. E-mail: pfister{at}nefo.med.uni-muenchen.de

Myeloid differentiation factor 88 (MyD88) is an essential intracellular signal transducer in Toll-like receptor (TLR) and interleukin (IL)-1 receptor family member-mediated cell activation. In order to characterize the role of MyD88 in pneumococcal meningitis we used gene-targeted mice lacking functional MyD88 expression. At 24 h after intracisternal infection, MyD88- deficient mice displayed a markedly diminished inflammatory host response in the CNS, as evidenced by reduced CSF pleocytosis and expression of cytokines, chemokines and complement factors. The reduced CNS inflammation was paralleled by a marked reduction in the prognostic relevant CNS complications, such as brain oedema formation. Nevertheless, MyD88 deficiency was associated with a worsening of disease which seemed to be attributable to severe bacteraemia. This notion was supported by the unexpected observation that infected MyD88-deficient mice displayed enhanced mRNA expression of inflammatory mediators [such as the proinflammatory cytokine tumour necrosis factor {alpha} (TNF-{alpha}) and the CXC chemokine macrophage inflammatory protein (MIP-2)] in the lung and consequently increased cell influx in the bronchoalveolar lavage fluid, compared with infected wild-type mice. Thus, the present study demonstrated for the first time an important role of MyD88 in immune activation to bacterial pathogens within the CNS. The role played by MyD88 in mounting an immune response to Streptococcus pneumoniae, however, seems to be dependent on the anatomical compartment involved.

Key Words: brain; lung; complement; inflammation; innate immunity

Abbreviations: BAL = bronchoalveolar lavage; BBB = blood–brain barrier; Crry = complement receptor-related protein y; ELISA = enzyme-linked immunosorbent assay; ICP = intracranial pressure; Ig = immunoglobulin; IL = interleukin; KC = keratinocyte-derived cytokine; MIP = macrophage inflammatory protein; MyD88 = myeloid differentiation factor 88; PBS = phosphate-buffered saline; TLR = Toll-like receptor; TNF = tumour necrosis factor

Received November 14, 2003. Revised February 3, 2004. Accepted February 14, 2004.


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