Abstract
PD-1 blockade therapy activates T cells by blocking the interaction between PD-1 and PD-L1 and promotes IFN-γ and Th1 cytokine production. In turn, IFN-γ and Th1 cytokines produced by activated T cells promote TF synthesis in monocytes/macrophages, which results in hypercoagulability leading to thrombosis.
Keywords:
Immune checkpoint blockade; Immune-related adverse event; Lung cancer; Tissue factor; Trousseau's syndrome.
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Case Reports
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Letter
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Research Support, Non-U.S. Gov't
MeSH terms
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Antibodies, Monoclonal, Humanized / adverse effects*
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Antibodies, Monoclonal, Humanized / therapeutic use
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Antineoplastic Agents, Immunological / adverse effects
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Antineoplastic Agents, Immunological / therapeutic use
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Blood Coagulation Disorders / chemically induced*
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Brain / diagnostic imaging
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Brain / pathology
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Carcinoma, Non-Small-Cell Lung / complications*
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Carcinoma, Non-Small-Cell Lung / therapy*
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Cerebral Infarction / chemically induced
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Cytokines / immunology
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Genes, cdc
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Humans
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Lymphocyte Activation
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Magnetic Resonance Imaging
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Male
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Middle Aged
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Neoplasm Metastasis
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Programmed Cell Death 1 Receptor / antagonists & inhibitors
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Thrombosis / diagnosis
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Thrombosis / etiology
Substances
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents, Immunological
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Cytokines
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PDCD1 protein, human
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Programmed Cell Death 1 Receptor
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pembrolizumab