Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells
Vito et al. investigated the effects of combination therapy in a TNBC tumor model and reported increased tumor-infiltrating lymphocytes that contributed to an improved response to immune checkpoint blockade. By depletion of circulating B cells prior to therapy, the authors showed a loss of therapeut...
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Nature Portfolio
2021
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oai:doaj.org-article:05222c9ff4534f789861496bd23f86ca2021-12-02T18:30:44ZImmune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells10.1038/s42003-021-02375-92399-3642https://doaj.org/article/05222c9ff4534f789861496bd23f86ca2021-07-01T00:00:00Zhttps://doi.org/10.1038/s42003-021-02375-9https://doaj.org/toc/2399-3642Vito et al. investigated the effects of combination therapy in a TNBC tumor model and reported increased tumor-infiltrating lymphocytes that contributed to an improved response to immune checkpoint blockade. By depletion of circulating B cells prior to therapy, the authors showed a loss of therapeutic efficacy and simultaneous expansion of myeloid-derived suppressor cells.Alyssa VitoOmar SalemNader El-SayesIan P. MacFawnAna L. PortilloKaty MilneDanielle HarringtonAli A. AshkarYonghong WanSamuel T. WorkenheBrad H. NelsonTullia C. BrunoKaren L. MossmanNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 4, Iss 1, Pp 1-19 (2021) |
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DOAJ |
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DOAJ |
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EN |
topic |
Biology (General) QH301-705.5 |
spellingShingle |
Biology (General) QH301-705.5 Alyssa Vito Omar Salem Nader El-Sayes Ian P. MacFawn Ana L. Portillo Katy Milne Danielle Harrington Ali A. Ashkar Yonghong Wan Samuel T. Workenhe Brad H. Nelson Tullia C. Bruno Karen L. Mossman Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells |
description |
Vito et al. investigated the effects of combination therapy in a TNBC tumor model and reported increased tumor-infiltrating lymphocytes that contributed to an improved response to immune checkpoint blockade. By depletion of circulating B cells prior to therapy, the authors showed a loss of therapeutic efficacy and simultaneous expansion of myeloid-derived suppressor cells. |
format |
article |
author |
Alyssa Vito Omar Salem Nader El-Sayes Ian P. MacFawn Ana L. Portillo Katy Milne Danielle Harrington Ali A. Ashkar Yonghong Wan Samuel T. Workenhe Brad H. Nelson Tullia C. Bruno Karen L. Mossman |
author_facet |
Alyssa Vito Omar Salem Nader El-Sayes Ian P. MacFawn Ana L. Portillo Katy Milne Danielle Harrington Ali A. Ashkar Yonghong Wan Samuel T. Workenhe Brad H. Nelson Tullia C. Bruno Karen L. Mossman |
author_sort |
Alyssa Vito |
title |
Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells |
title_short |
Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells |
title_full |
Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells |
title_fullStr |
Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells |
title_full_unstemmed |
Immune checkpoint blockade in triple negative breast cancer influenced by B cells through myeloid-derived suppressor cells |
title_sort |
immune checkpoint blockade in triple negative breast cancer influenced by b cells through myeloid-derived suppressor cells |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/05222c9ff4534f789861496bd23f86ca |
work_keys_str_mv |
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