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pubmed-article:18317964pubmed:abstractTextA transgenic mouse model of autochthonous mammary carcinoma was chosen to study the impact of tumor progression on the immune system over an extended period. We found: i) that splenocyte numbers, particularly myeloid cells, increased concurrently with tumor burden; ii) the percentage of tumor-infiltrating Treg cells was similar to that in human breast cancer; iii) suppressed T cell proliferation and cytokine production and; iv) significantly elevated MCP-1 and TNF-alpha in the sera of tumor-bearing mice. The modified immune status in these tumor-bearing hosts is consistent with a "syndrome" that likely impacts the efficacy of cancer immunosurveillance and response to therapy.lld:pubmed
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pubmed-article:18317964pubmed:articleTitleImmune consequences of protracted host-tumor interactions in a transgenic mouse model of mammary carcinoma.lld:pubmed
pubmed-article:18317964pubmed:affiliationLaboratory of Tumor Immunology and Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.lld:pubmed
pubmed-article:18317964pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18317964pubmed:publicationTypeResearch Support, N.I.H., Intramurallld:pubmed
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