Ulf Yrlid Göteborgs universitet
Ulf Yrlid Göteborgs universitet
Image captured at the NIAID Integrated Research Facility (IRF) in Fort Detrick, Maryland. Introduction: CD47 is an anti-phagocytic ('don't eat me') signal overexpressed in many malignant diseases. It acts as myeloid immune checkpoint and thus has prognostic and therapeutic implications. Methods: A novel peptide pep-20, specifically targeting CD47 and blocking CD47/SIRPα interaction, was identified via high-throughput phage display library bio-panning. The capability to enhance the macrophage-mediated phagocytosis activities and antitumor effects of pep-20 were investigated. CD47, a ‘marker-of-self’ protein that is overexpressed broadly across tumor types, is emerging as a novel potent macrophage immune checkpoint for cancer immunotherapy. Recently, CD47 blockade by Hu5F9-G4 has shown promise combined with Rituximab in non-Hodgkin’s lymphoma.
Inhibitors of the CD47-SIRPα interaction improve antitumor antibody responses by enhancing antibody-dependent cellular p … The role of CD47-SIRPα immune checkpoint in tumor immune evasion and innate immunotherapy As a transmembrane protein, CD47 plays an important role in mediating cell proliferation, migration, phagocytosis, apoptosis, immune homeostasis, inhibition of NO signal transduction and other related reactions. Immunohistochemistry and flow cytometry were used to measure CD47 ("don't eat me signal") expression on tumor cells and characterize macrophages in the tumor microenvironment. In vitro engulfment assays and mouse experiments were performed with CD47-blocking antibodies to assess macrophage engulfment of tumor cells, progression of micrometastases in the liver and mouse survival. As important innate immune cells, macrophages play important roles in maintaining homeostasis, preventing pathogen invasion, resisting tumor cells and promoting adaptive immune response. CD47 is found to be overexpressed on tumor cells and act as a don't eat me' signal, which contributes to immune evasion.
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Anti-SIRP alpha antibodies as a potential new tool for cancer immunotherapy Furthermore, an anti-SIRP alpha Ab that blocks the interaction with CD47 Cell indexvärdet från brunnar med CD47-CAR T-celler ensamt Weiskopf, K. Cancer immunotherapy targeting the CD47/SIRPalpha axis. regulated PD-1/PD-L1 immune checkpoint blockade immunotherapy in colon and macrophages via inflammatory mediators and CD47 promotes tumour cell då man prövat interleukin 2, onkolytiska virus, ”checkpoint”-blockad, TGF-beta-inhibitorer, neoantigenvacciner och CD47-blockad3.
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Mar 6, 2020 The gut microbiome modulates gut immunity and affects the host response to cancer immunotherapy, but how microbiota influence the tumor Moreover, MM cells had remarkably higher CD47 expression than other cell that macrophage checkpoint immunotherapy by blocking the CD47 “don't eat me” Jul 26, 2019 The CD47/SIRPα axis is therefore a known major pathway for immune evasion by tumor cells, and is being investigated as an immunotherapy Oct 31, 2018 Anti-CD47 cancer therapy safe, shows promise in small clinical trial. An immunotherapy conceived at Stanford appeared safe in an early Sep 9, 2020 the latest in a string of large biopharma companies making moves into the emerging space of cancer immunotherapy drugs targeting CD47. Aug 28, 2018 Tumor immunotherapy targeting CD47/SIRPα axis has been one hotspot in cancer therapy. Here, we summarize the preclinical evidence and Apr 18, 2018 The CD47 immune checkpoint represents a potentially effective and widely applicable target for cancer immunotherapy, and therefore a Sep 19, 2017 Inhibitors of the CD47–SIRPα interaction improve antitumor antibody responses The success of combination immunotherapy involving CD47 Sep 22, 2020 Scholars have clarified the mechanism of action of CD47-SIRPα, and macrophage-mediated tumor immunotherapy has gained increasing Sep 4, 2020 The cancer protein CD47 is a hot target for drug developers, but it's not immunotherapy developer and its lead CD47 inhibitor, magrolimab.
Mar 6, 2020 The gut microbiome modulates gut immunity and affects the host response to cancer immunotherapy, but how microbiota influence the tumor
Moreover, MM cells had remarkably higher CD47 expression than other cell that macrophage checkpoint immunotherapy by blocking the CD47 “don't eat me”
Jul 26, 2019 The CD47/SIRPα axis is therefore a known major pathway for immune evasion by tumor cells, and is being investigated as an immunotherapy
Oct 31, 2018 Anti-CD47 cancer therapy safe, shows promise in small clinical trial.
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CD47, a multi-facetted target for cancer immunotherapy.
1/2 inhibitors, BCL-2 inhibitors, and CD47 antibodies—are being investigated to Stephen V. Liu, MD / Bhavesh Shah, RPh, BCOP - Immunotherapy in the
CD47 promotes neuronal development through Src- and FRG/Vav2-mediated Anti-human SIRP antibody is a new tool for cancer immunotherapy2018Ingår i:
CD47 expression CD47, the expression of which is ubiquitous, The goal of immunotherapy is to re-educate the immune system and to
A possible immunotherapy in acute myeloid leukemia via combination of "drugs" in cancer cell migration by macrophage derived factors via CD47 and EGFR.
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Anti-SIRP alpha antibodies as a potential new tool for cancer
CD-47 acts as a don't eat me signal to macrophages of the immune system The CD47 gene is located on chromosome 3q13 and encodes an integrin-associated protein. CD47 is an important “self-labeling” molecule in the immunoglobulin superfamily that contains an immunoglobulin variable-like amino-terminal domain, five transmembrane … 2018-03-15 2019-04-18 Wiersma VR, van Bommel PE, de Bruyn M, et al. CD47, a multi-facetted target for cancer immunotherapy. Atlas of Genetics and Cytogenetics in Oncology and Haematology website. http ancer immune responses. Here, we treated carcinogen-induced or transplantable mouse models of cancer by a CD47 blocking antibody that was at least as efficient as chemotherapy and that could be favorably combined with the anthracycline mitoxantrone in the context of carcinogen-induced ortho- 2021-03-01 2021-03-17 2019-03-14 2018-08-28 Multiple myeloma (MM) remains to be incurable despite recent therapeutic advances.
Immunterapi mot cancer - Cancer immunotherapy - qaz.wiki
CD47, a multi-facetted target for cancer immunotherapy. Atlas of Genetics and Cytogenetics in Oncology and Haematology website. http 2018-12-11 · Monotherapy by CD47 blockade led to a reduction in tumor growth and an increase in overall survival. Of note, this treatment lead to a moderate depletion of M2 macrophages as well as close-to-complete elimination of regulatory T cells from the tumor bed, suggesting a strong favorable impact of CD47 blockade on the tumor microenvironment. The suppressive effect of macrophages was enhanced by blocking CD47 on pancreatic cancer cells, leading to decreased metastatic burden and prolonged survival. This work supports a clinical trial of CD47 blockade as an adjuvant immunotherapy for pancreatic cancer. 2019-03-14 · Targeting CD47 or CD274 (PD-L1) is very commonly used in immune checkpoint therapy.
2020-10-01 The CD47/signal regulatory protein alpha (SIRPα) axis is a critical regulator of myeloid cell activation and serves a broader role as a myeloid-specific immune checkpoint. CD47 is highly expressed on many different types of cancer, and it transduces inhibitory signals through SIRPα on … PDF | On Apr 1, 2017, Valerie R Wiersma and others published CD47, a multi-facetted target for cancer immunotherapy | Find, read and cite all the research you need on ResearchGate 2019-12-11 CD47 antibody retards the growth of spontaneous tumors. Medroxyprogesterone acetate (MPA) pellets (50 mg, 90-day release) were implanted subcutaneously into the interscapular area of However, immunotherapies related to innate responses such as CD47 blockade rely on the rapid immune responses within the tumor microenvironment.