6 research outputs found

    A Prosecutor\u27s Perspective

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    4 - A Prosecutor\u27s Perspective

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    Michael R. Juviler writes about Terry v Ohio from the perspective of a litigator preparing for the Supreme Court as well as from the perspective of a trial judge who has been applying the Terry case and the cases decided after it

    4 - A Prosecutor\u27s Perspective

    No full text
    Michael R. Juviler writes about Terry v Ohio from the perspective of a litigator preparing for the Supreme Court as well as from the perspective of a trial judge who has been applying the Terry case and the cases decided after it

    A Prosecutor\u27s Perspective

    No full text

    GM-CSF drives myelopoiesis, recruitment and polarisation of tumour-associated macrophages in cholangiocarcinoma and systemic blockade facilitates antitumour immunity.

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    OBJECTIVE: Intrahepatic cholangiocarcinoma (iCCA) is rising in incidence, and at present, there are limited effective systemic therapies. iCCA tumours are infiltrated by stromal cells, with high prevalence of suppressive myeloid populations including tumour-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs). Here, we show that tumour-derived granulocyte-macrophage colony-stimulating factor (GM-CSF) and the host bone marrow is central for monopoiesis and potentiation of TAMs, and abrogation of this signalling axis facilitates antitumour immunity in a novel model of iCCA. METHODS: Blood and tumours were analysed from iCCA patients and controls. Treatment and correlative studies were performed in mice with autochthonous and established orthotopic iCCA tumours treated with anti-GM-CSF monoclonal antibody. RESULTS: Systemic elevation in circulating myeloid cells correlates with poor prognosis in patients with iCCA, and patients who undergo resection have a worse overall survival if tumours are more infiltrated with CD68 CONCLUSIONS: iCCA uses the GM-CSF-bone marrow axis to establish an immunosuppressive tumour microenvironment. Blockade of the GM-CSF axis promotes antitumour T cell immunity
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