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10.1158/2326-6066.CIR-16-0221

http://scihub22266oqcxt.onion/10.1158/2326-6066.CIR-16-0221
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C5510552!5510552!28533311
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suck abstract from ncbi


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pmid28533311      Cancer+Immunol+Res 2017 ; 5 (7): 560-70
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  • Converting lymphoma cells into potent antigen-presenting cells for interferon-induced tumor regression #MMPMID28533311
  • Liao J; Luan Y; Ren Z; Liu X; Xue D; Xu H; Sun Z; Yang K; Peng H; Fu YX
  • Cancer Immunol Res 2017[Jul]; 5 (7): 560-70 PMID28533311show ga
  • Anti-hCD20 is a therapeutic monoclonal antibody (mAb) that is clinically used to treat B-cell lymphoma. Some lymphomas are resistant to anti-hCD20; others relapse after treatment with anti-hCD20. Using a syngeneic immunocompetent mouse model, we observed that targeting lymphoma with interferon-? (IFN?) abolished resistance of B-cell lymphoma to anti-CD20 while limiting interferon (IFN)-associated systemic toxicity in the host. Control of tumors by a fusion of anti-CD20 and IFN? (anti-CD20-IFN?) depended on existing tumor-infiltrating CD8+ T cells. Although lymphomas were resistant to IFN-directed killing, IFN-exposed tumor cells became the dominant antigen-presenting cells (APCs) for the reactivation of tumor-infiltrating CD8+ T cells that then controlled those lymphomas. Anti-CD20-IFN? also abolished checkpoint blockade resistance in advanced B-cell lymphoma. Our findings indicate that anti-CD20-IFN? eradicates B-cell lymphoma by employing tumor cells as APCs to reactivate tumor-infiltrating CD8+ T cells and synergizing with anti-PD-L1 treatment.
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