A review of the importance of immune responses in luminal B breast cancer
dc.contributor.author | Nelson, Delia | |
dc.contributor.author | Clark, B. | |
dc.contributor.author | Munyard, K. | |
dc.contributor.author | Williams, V. | |
dc.contributor.author | Groth, David | |
dc.contributor.author | Gill, J. | |
dc.contributor.author | Preston, H. | |
dc.contributor.author | Chan, A. | |
dc.date.accessioned | 2017-11-24T05:25:58Z | |
dc.date.available | 2017-11-24T05:25:58Z | |
dc.date.created | 2017-11-24T04:48:42Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Nelson, D. and Clark, B. and Munyard, K. and Williams, V. and Groth, D. and Gill, J. and Preston, H. et al. 2017. A review of the importance of immune responses in luminal B breast cancer. OncoImmunology. 6 (3). | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/58478 | |
dc.identifier.doi | 10.1080/2162402X.2017.1282590 | |
dc.description.abstract |
© 2017 Taylor & Francis Group, LLC. Historically, the immune environment was not considered an important target for breast cancer treatment. However, the association of lymphocytic infiltrates in triple negative and HER-2 over-amplified breast cancer subtypes with better outcomes, has provoked interest in evaluating the role of the immune system in the luminal B subtype that accounts for 39% of breast cancers and has a poor patient prognosis. It is unknown which immunosuppressive cell types or molecules (e.g., checkpoint molecules) are relevant, or where measurement is most informative. We hypothesize that a profound immunosuppressive tumor and/or lymph node milieu is prognostic and impacts on responses to therapies. | |
dc.publisher | Landes Bioscience | |
dc.title | A review of the importance of immune responses in luminal B breast cancer | |
dc.type | Journal Article | |
dcterms.source.volume | 6 | |
dcterms.source.number | 3 | |
dcterms.source.issn | 2162-4011 | |
dcterms.source.title | OncoImmunology | |
curtin.department | School of Biomedical Sciences | |
curtin.accessStatus | Fulltext not available |
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