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Michael Quigley

Researcher at Bristol-Myers Squibb

Publications -  26
Citations -  1814

Michael Quigley is an academic researcher from Bristol-Myers Squibb. The author has contributed to research in topics: Immune system & Tumor microenvironment. The author has an hindex of 12, co-authored 25 publications receiving 1350 citations. Previous affiliations of Michael Quigley include Janssen Pharmaceutica.

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Anti-CTLA-4 antibodies of IgG2a isotype enhance antitumor activity through reduction of intratumoral regulatory T cells.

TL;DR: Data suggest that anti-CTLA-4 promotes antitumor activity by a selective reduction of intratumoral Tregs along with concomitant activation of Teffs.
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Preclinical Development of Ipilimumab and Nivolumab Combination Immunotherapy: Mouse Tumor Models, In Vitro Functional Studies, and Cynomolgus Macaque Toxicology

TL;DR: In vitro studies with combined ipilimumab and nivolumab showed enhanced cytokine secretion in superantigen stimulation of human peripheral blood lymphocytes and in mixed lymphocyte response assays, and dose-dependent immune-related gastrointestinal inflammation was observed with the combination therapy; this response had not been observed in previous single agent cynomolgus studies.
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PD-1/PD-L1 interactions contribute to functional T-cell impairment in patients who relapse with cancer after allogeneic stem cell transplantation.

TL;DR: The findings indicate that the PD-1/PD-L pathway can be hijacked as an immune escape mechanism in hematological malignancies and suggest that blocking thePD-1 immune checkpoint offers an appealing immunotherapeutic strategy following alloSCT in patients with recurrent or relapsed disease.
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Combination of CD40 Agonism and CSF-1R Blockade Reconditions Tumor-Associated Macrophages and Drives Potent Antitumor Immunity

TL;DR: It is demonstrated that combining therapeutic approaches may simultaneously remove inhibitory immune populations and sustain endogenous antitumor immune responses to successfully impair cancer progression and provide rationale for the combination of two distinct immunotherapies to improve clinical outcome.