Title |
Engrafted human cells generate adaptive immune responses to Mycobacterium bovis BCG infection in humanized mice
|
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Published in |
BMC Immunology, December 2013
|
DOI | 10.1186/1471-2172-14-53 |
Pubmed ID | |
Authors |
Jinhee Lee, Michael A Brehm, Dale Greiner, Leonard D Shultz, Hardy Kornfeld |
Abstract |
Currently used mouse models fail to fully reflect human immunity to tuberculosis (TB), which hampers progress in research and vaccine development. Bone marrow-liver-thymus (BLT) mice, generated by engrafting human fetal liver, thymus, and hematopoietic stem cells in severely immunodeficient NOD/SCID/IL-2Rγ(-/-) (NSG) mice, have shown potential to model human immunity to infection. We engrafted HLA-A2-positive fetal tissues into NSG mice transgenically expressing human leukocyte antigen (HLA)-A2.1 (NSG-A2) to generate NSG-A2-BLT mice and characterized their human immune response to Mycobacterium bovis bacillus Calmette-Guerin (BCG) infection to assess the utility of this model for investigating human TB. |
X Demographics
Geographical breakdown
Country | Count | As % |
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United Kingdom | 1 | 50% |
Unknown | 1 | 50% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 1 | 50% |
Science communicators (journalists, bloggers, editors) | 1 | 50% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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Germany | 1 | 2% |
Unknown | 56 | 98% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Ph. D. Student | 15 | 26% |
Researcher | 13 | 23% |
Student > Master | 6 | 11% |
Student > Bachelor | 6 | 11% |
Other | 4 | 7% |
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Unknown | 6 | 11% |
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Neuroscience | 3 | 5% |
Other | 7 | 12% |
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