Bacteria remain a major cause of human disease and a formidable foe of the mammalian immune system. Bacter-ial entry into normally sterile compartments has long been recognized as a potential calamity for the mammalian host, in the most extreme circumstances resulting in circulatory collapse and multiorgan failure. In contrast to viruses, most bacteria are self-sufficient, producing their own lipid membranes, cell walls, nucleic acids, and proteins. Although many synthetic pathways used by bacteria and mammals are similar, others are subtly different and some are completely distinct. The mammalian immune system has evolved an array of mechanisms to recognize and respond to these distinct bacterial products upon infection. While it has been appreciated for over a century that the mammalian immune system uses receptors to specifically recognize bacterial products and initiate inflammatory defenses upon infection, the last decade has witnessed...
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Commentary|
May 21 2001
Cd8 T Cell Detection of Bacterial Infection: Sniffing for Formyl Peptides Derived from Mycobacterium tuberculosis
Gregoire Lauvau,
Gregoire Lauvau
aInfectious Disease Service, Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021
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Eric G. Pamer
Eric G. Pamer
aInfectious Disease Service, Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021
Search for other works by this author on:
Gregoire Lauvau
,
Eric G. Pamer
aInfectious Disease Service, Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021
Received:
April 16 2001
Accepted:
April 23 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 193 (10): F35–F40.
Article history
Received:
April 16 2001
Accepted:
April 23 2001
Citation
Gregoire Lauvau, Eric G. Pamer; Cd8 T Cell Detection of Bacterial Infection: Sniffing for Formyl Peptides Derived from Mycobacterium tuberculosis. J Exp Med 21 May 2001; 193 (10): F35–F40. doi: https://doi.org/10.1084/jem.193.10.F35
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