Synergistic innate and adaptive immune response to combination immunotherapy with anti-tumor antigen antibodies and extended serum half-life IL-2.

Synergistic innate and adaptive immune response to combination immunotherapy with anti-tumor antigen antibodies and extended serum half-life IL-2.
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DOI:
10.1016/j.ccell.2015.03.004
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发表时间:
2015-04-13
期刊:
影响因子:
50.3
通讯作者:
Wittrup KD
Wittrup KD
中科院分区:
医学1区
文献类型:
--
作者:
Zhu EF;Gai SA;Opel CF;Kwan BH;Surana R;Mihm MC;Kauke MJ;Moynihan KD;Angelini A;Williams RT;Stephan MT;Kim JS;Yaffe MB;Irvine DJ;Weiner LM;Dranoff G;Wittrup KD

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Cancer immunotherapies under development have generally focused on either stimulating T-cell immunity or driving antibody-directed effector functions of the innate immune system such as antibody-dependent cell-mediated cytotoxicity (ADCC). We find that a combination of an anti-tumor antigen antibody and an untargeted IL-2 fusion protein with delayed systemic clearance induces significant tumor control in aggressive isogenic tumor models via a concerted innate and adaptive response involving neutrophils, NK cells, macrophages, and CD8+ T-cells. This combination therapy induces an intratumoral “cytokine storm” and extensive lymphocyte infiltration. Adoptive transfer of anti-tumor T-cells together with this combination therapy leads to robust cures of established tumors and establishment of immunological memory.
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