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      Nanodrugs Targeting T Cells in Tumor Therapy

      review-article

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          Abstract

          In contrast to conventional anti-tumor agents, nano-carriers allow co-delivery of distinct drugs in a cell type-specific manner. So far, many nanodrug-based immunotherapeutic approaches aim to target and kill tumor cells directly or to address antigen presenting cells (APC) like dendritic cells (DC) in order to elicit tumor antigen-specific T cell responses. Regulatory T cells (Treg) constitute a major obstacle in tumor therapy by inducing a pro-tolerogenic state in APC and inhibiting T cell activation and T effector cell activity. This review aims to summarize nanodrug-based strategies that aim to address and reprogram Treg to overcome their immunomodulatory activity and to revert the exhaustive state of T effector cells. Further, we will also discuss nano-carrier-based approaches to introduce tumor antigen-specific chimeric antigen receptors (CAR) into T cells for CAR-T cell therapy which constitutes a complementary approach to DC-focused vaccination.

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          Most cited references186

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          Axicabtagene Ciloleucel CAR T-Cell Therapy in Refractory Large B-Cell Lymphoma

          In a phase 1 trial, axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy, showed efficacy in patients with refractory large B-cell lymphoma after the failure of conventional therapy.
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            Combined Nivolumab and Ipilimumab or Monotherapy in Untreated Melanoma

            New England Journal of Medicine, 373(1), 23-34
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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
                25 May 2022
                2022
                : 13
                : 912594
                Affiliations
                [1]University Medical Center Mainz, Department of Dermatology , Mainz, Germany
                Author notes

                Edited by: Robert Zeiser, University of Freiburg, Germany

                Reviewed by: Rebecca Kesselring, University of Freiburg Medical Center, Germany; Tifeng Jiao, Yanshan University, China

                *Correspondence: Matthias Bros, mbros@ 123456uni-mainz.de

                This article was submitted to Vaccines and Molecular Therapeutics, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2022.912594
                9174908
                35693776
                7a65de65-78ea-4ab5-8686-4fac00189e87
                Copyright © 2022 Haist, Mailänder and Bros

                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
                : 05 April 2022
                : 27 April 2022
                Page count
                Figures: 2, Tables: 1, Equations: 0, References: 186, Pages: 21, Words: 11785
                Categories
                Immunology
                Review

                Immunology
                nanodrug,nanoparticle,t cell,regulatory t cell,immunotherapy,car-t cell,mrna,melanoma
                Immunology
                nanodrug, nanoparticle, t cell, regulatory t cell, immunotherapy, car-t cell, mrna, melanoma

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