机构:
Univ British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, CanadaUniv British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, Canada
Hestvik, ALK
[1
]
Hmama, Z
论文数: 0引用数: 0
h-index: 0
机构:
Univ British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, CanadaUniv British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, Canada
Hmama, Z
[1
]
Av-Gay, Y
论文数: 0引用数: 0
h-index: 0
机构:
Univ British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, CanadaUniv British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, Canada
Av-Gay, Y
[1
]
机构:
[1] Univ British Columbia, Dept Med, Div Infect Dis, Vancouver, BC V5Z 3J5, Canada
Phagosome biogenesis, the process by which macrophages neutralize ingested pathogens and initiate antigen presentation, has entered the field of cellular mycobacteriology research largely owing to the discovery 30 years ago that phagosomes harboring mycobacteria are refractory to fusion with lysosomes. In the past decade, the use of molecular genetics and biology in different model systems to study phagosome biogenesis have made significant advances in understanding subtle mechanisms by which mycobacteria inhibit the maturation of its phagosome. Thus, we are beginning to appreciate the extent to which these pathogens are able to interfere with innate immune responses and manipulate defense mechanisms to enhance their survival within the human host cell. Here, we summarize current knowledge about phagosome maturation arrest in infected macrophages and the subsequent attenuation of the macrophave-initiated adaptive anti-mycobacterial immune defenses. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.