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Fate of Mycobacterium tuberculosis within Murine Dendritic Cells

Open access
Bodnar, Kendra A., Serbina, Natalya V., Flynn, JoAnne L.·2001·Infection and Immunity

Abstract

The interaction of microbes with dendritic cells (DCs) is likely to have an enormous impact on the initiation of the immune response against a pathogen. In this study, we compared the interaction of Mycobacterium tuberculosis with murine bone marrow-derived DCs and macrophages (Mφ) in vitro.M. tuberculosis grew equally well within nonactivated DCs and Mφ. Activation of DCs and Mφ with gamma interferon and lipopolysaccharide inhibited the growth of the intracellular bacteria in a nitric oxide synthase-dependent fashion. However, while this activation enabled Mφ to kill the intracellular bacteria, the M. tuberculosis bacilli within activated DCs were not killed. Thus, DCs could restrict the growth of the intracellular mycobacteria but were less efficient than Mφ at eliminating the infection. These results may have implications for priming immune responses to M. tuberculosis. In addition, they suggest that DCs may serve as a reservoir for M. tuberculosis in tissues, including the lymph nodes and lungs.

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Metadata

Authors
Bodnar, K. A., Serbina, N. V., & Flynn, J. L.
Venue
Infection and Immunity
Published
2001-02
Volume
69
Issue
2
Pages
800-809
ISSN
  • 0019-9567 (ISSN-L)
  • 1098-5522
OpenAlex
W2130615964
Cited by
213
References
0
FWCI
13.57
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Fate of Mycobacterium tuberculosis within Murine Dendritic Cells. https://app.cochat.ai/papers/10.1128/iai.69.2.800-809.2001
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Bodnar, K. A., Serbina, N. V., & Flynn, J. L. (2001). Fate of Mycobacterium tuberculosis within Murine Dendritic Cells. Infection and Immunity. https://doi.org/10.1128/iai.69.2.800-809.2001

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.