Innate and Non-Classical Immune Cells in Cancer Immunotherapy
Mar 24–28, 2019 | Keystone Resort, Keystone, CO, United States
Scientific Organizers:
Nicholas D. Huntington, Eric Vivier, Caroline Robert and Lewis L. Lanier
In Person
Mar 24–28, 2019 | Keystone Resort, Keystone, CO, United States
Scientific Organizers:
Nicholas D. Huntington, Eric Vivier, Caroline Robert and Lewis L. Lanier
Available Formats:
Supported by the Directors' Fund
In Person
Important Deadlines
Early Registration Deadline:
January 23, 2019
Scholarship Deadline:
December 4, 2018
Global Health Award Deadline:
Deadlines not yet available for this meeting.
Short Talk Abstract Deadline:
Deadlines not yet available for this meeting.
Poster Abstract Deadline:
December 4, 2018
Meeting Summary
# Cancer
# Immunology
Immunotherapy has revolutionized the treatment of many cancer types over the past five years. T cell checkpoint inhibitors have led the way and are the focus of most immunotherapy trials. However innate and non-classical T cells contribute extensively to the tumor infiltrate and significantly impact on the tumor immune response in both the tumor microenvironment and in circulation. This symposium aims to bring together academic and industry opinion leaders in the fields of innate immune cells, natural killer cells, tumor microenvironment, tumor immune suppression, novel immunotherapeutic strategies and clinical cancer immunotherapy to define the next wave of immunotherapy breakthroughs that reach beyond the current T cell checkpoints. The conference offers a unique opportunity for an audience of diverse immunology and cancer research backgrounds to come together and share cutting edge insights into cancer immunology and rational approaches for therapeutic intervention that could be used as be standalone therapy or in combination with T cell checkpoint therapies. A key aim is to bring together experts with complementary interest in cancer immunotherapy that would not normally be drawn to common symposia and foster new dynamic collaborations to advance our understanding of tumor immunity.
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KEYSTONE SYMPOSIA THANKS THESE DONOR(S) FOR GENEROUSLY SUPPORTING THIS MEETING:
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GRANT RECOGNITION:
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