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John J. Engelhardt

Researcher at Bristol-Myers Squibb

Publications -  20
Citations -  1757

John J. Engelhardt is an academic researcher from Bristol-Myers Squibb. The author has contributed to research in topics: Antibody & Immune system. The author has an hindex of 8, co-authored 19 publications receiving 1381 citations. Previous affiliations of John J. Engelhardt include University of California, San Francisco.

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Journal ArticleDOI

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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Marginating Dendritic Cells of the Tumor Microenvironment Cross-present Tumor Antigens and Stably Engage Tumor-Specific T cells

TL;DR: It is determined that infiltrating tumor-specific T cells engage in long-lived interactions with bone-marrow-derived cells, proximal to the tumor, and spatiotemporal dynamics revealed here implicate nonproductive interactions between T-cells and antigen-presenting cells on the tumor margin.
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FcγRs Modulate the Anti-tumor Activity of Antibodies Targeting the PD-1/PD-L1 Axis

TL;DR: It is revealed that distinct Fcγ receptor (FcγRs) dependency and mechanisms account for the in vivo activity of anti- PD-1 versus anti-PD-L1 Abs, which show augmented anti-tumor activity when activating F cγR binding is introduced into the molecules.
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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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Antitumor activity of concurrent blockade of immune checkpoint molecules CTLA-4 and PD-1 in preclinical models.

TL;DR: The evaluation of concurrent treatment with anti-PD-1 and anti-CTLA-4 mAbs in preclinical models results in synergistic antitumor activity whereas efficacy with sequential dosing wa...