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      Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle

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          Abstract

          Triple-negative breast cancer (TNBC) remains difficult to treat, especially due to ineffective immune responses. Current treatments mainly aim at a cytotoxic effect, whereas (stem) cell therapies are being investigated for their immune stimulatory capacities to initiate the anti-tumor immunity. Here, a thoroughly characterized, homogenous and non-tumorigenic mixture of equine mesenchymal stem cells (eMSCs) harvested from horse peripheral blood as innovative xenogeneic immunomodulators were tested in a 4T1-based intraductal mouse model for TNBC. The eMSCs significantly reduced 4T1 progression upon systemic injection, with induction of inflammatory mediators and T-cell influx in primary tumors, already after a single dose. These xenogeneic anti-cancer effects were not restricted to MSCs as systemic treatment with alternative equine epithelial stem cells (eEpSCs) mimicked the reported disease reduction. Mechanistically, effective eMSC treatment did not rely on the spleen as systemic entrapment site, whereas CD4 + and CD8α + T-cell infiltration and activation were critical. These results show that eMSCs and potentially also other equine stem cell types can be a valuable TNBC treatment strategy for further (pre)clinical evaluation.

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          Oncology meets immunology: the cancer-immunity cycle.

          The genetic and cellular alterations that define cancer provide the immune system with the means to generate T cell responses that recognize and eradicate cancer cells. However, elimination of cancer by T cells is only one step in the Cancer-Immunity Cycle, which manages the delicate balance between the recognition of nonself and the prevention of autoimmunity. Identification of cancer cell T cell inhibitory signals, including PD-L1, has prompted the development of a new class of cancer immunotherapy that specifically hinders immune effector inhibition, reinvigorating and potentially expanding preexisting anticancer immune responses. The presence of suppressive factors in the tumor microenvironment may explain the limited activity observed with previous immune-based therapies and why these therapies may be more effective in combination with agents that target other steps of the cycle. Emerging clinical data suggest that cancer immunotherapy is likely to become a key part of the clinical management of cancer. Copyright © 2013 Elsevier Inc. All rights reserved.
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            Elements of cancer immunity and the cancer–immune set point

            Immunotherapy is proving to be an effective therapeutic approach in a variety of cancers. But despite the clinical success of antibodies against the immune regulators CTLA4 and PD-L1/PD-1, only a subset of people exhibit durable responses, suggesting that a broader view of cancer immunity is
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              Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer

              Unresectable locally advanced or metastatic triple-negative (hormone-receptor-negative and human epidermal growth factor receptor 2 [HER2]-negative) breast cancer is an aggressive disease with poor outcomes. Nanoparticle albumin-bound (nab)-paclitaxel may enhance the anticancer activity of atezolizumab.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                20 October 2023
                2023
                : 14
                : 1252374
                Affiliations
                [1] 1 Laboratory of Biochemistry, Department of Veterinary and Biosciences, Faculty of Veterinary Medicine, Ghent University , Merelbeke, Belgium
                [2] 2 Cancer Research Institute Ghent (CRIG) , Ghent, Belgium
                [3] 3 Boehringer Ingelheim Veterinary Medicine Belgium , Evergem, Belgium
                [4] 4 Small Animal Department, Faculty of Veterinary Medicine, Ghent University , Merelbeke, Belgium
                [5] 5 Laboratory of Gene Therapy, Department of Veterinary and Biosciences, Faculty of Veterinary Medicine, Ghent University , Merelbeke, Belgium
                [6] 6 Department of Morphology, Imaging, Orthopedics, Rehabilitation and Nutrition, Faculty of Veterinary Medicine, Ghent University , Merelbeke, Belgium
                [7] 7 Boehringer-Ingelheim Animal Health USA , Athens, GA, United States
                Author notes

                Edited by: Sina Naserian, Hôpital Paul Brousse, France

                Reviewed by: Concha Herrera, Hospital Reina Sofía de Córdoba, Spain; Amira Bouzidi, ScreenCell, France

                *Correspondence: Jonas Steenbrugge, Jonas.Steenbrugge@ 123456ugent.be

                †These authors share last authorship

                Article
                10.3389/fimmu.2023.1252374
                10623058
                19f05a63-4758-4f37-af3e-11ffaed06877
                Copyright © 2023 Steenbrugge, Pauwelyn, Demeyere, Devriendt, de Rooster, Sanders, Spaas and Meyer

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 03 July 2023
                : 03 October 2023
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 59, Pages: 14, Words: 7525
                Funding
                This work was in part supported by a junior postdoctoral fellowship from the Research Foundation Flanders (FWO, 12Y3122N) awarded to JS, a grant from the Fund Suzanne Duchesne (managed by the King Baudouin Foundation) awarded to JS and a grant from the Research Foundation Flanders (FWO, G.0621.10) awarded to NNS.
                Categories
                Immunology
                Original Research
                Custom metadata
                Cancer Immunity and Immunotherapy

                Immunology
                triple-negative breast cancer,intraductal model,immunotherapy,xenogeneic,equine stem cells

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