Advancements in Cancer Immunotherapy beyond Checkpoint Blockade

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Immunology".

Deadline for manuscript submissions: closed (31 March 2024) | Viewed by 1471

Special Issue Editors

Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, AL, USA
Interests: chronic illness; cancer chemoprevention; UV radiation; DNA damage; immunosuppression; microRNAs; epigenetics
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Guest Editor
Department of Otolaryngology, School of Medicine, Emory University, Atlanta, GA, USA
Interests: head and neck cancer; pancreatic cancer; cancer biology; metalloproteinases; molecular biology

Special Issue Information

Dear Colleagues,

The advent of T-cell checkpoint inhibitors has revolutionized cancer therapy, leading to increased survival rates and even complete remission for numerous cancer patients. Despite their ability to enhance CD8+ T cell responses, other immune cell populations have been identified as potential targets for improving outcomes in cancer patients. Manipulating myeloid cells and other lymphocytes in pre-clinical models has demonstrated promising results in impeding cancer progression. This special issue aims to showcase the latest developments in immunotherapy targets that extend beyond CD8+ T cells.

Therefore, we would like to invite you all to contribute an original paper or a review paper on recent novel concepts based on basic and/or clinical research to understand role of various immune cells for the better management of cancers, a deadliest disease accounting over 10 million deaths worldwide, annually.

Dr. Ram Prasad
Dr. Vikash Kansal
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cells is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • T-cell function in cancer
  • immune checkpoint blockade
  • CD8+ T cell responses
  • myeloid cells
  • immunotherapy targets
  • cancer progression

Published Papers (1 paper)

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22 pages, 2895 KiB  
Review
State of the Art in CAR-T Cell Therapy for Solid Tumors: Is There a Sweeter Future?
by Beatriz Amorós-Pérez, Benigno Rivas-Pardo, Manuel Gómez del Moral, José Luis Subiza and Eduardo Martínez-Naves
Cells 2024, 13(9), 725; https://doi.org/10.3390/cells13090725 - 23 Apr 2024
Viewed by 1119
Abstract
Chimeric antigen receptor (CAR)-T cell therapy has proven to be a powerful treatment for hematological malignancies. The situation is very different in the case of solid tumors, for which no CAR-T-based therapy has yet been approved. There are many factors contributing to the [...] Read more.
Chimeric antigen receptor (CAR)-T cell therapy has proven to be a powerful treatment for hematological malignancies. The situation is very different in the case of solid tumors, for which no CAR-T-based therapy has yet been approved. There are many factors contributing to the absence of response in solid tumors to CAR-T cells, such as the immunosuppressive tumor microenvironment (TME), T cell exhaustion, or the lack of suitable antigen targets, which should have a stable and specific expression on tumor cells. Strategies being developed to improve CAR-T-based therapy for solid tumors include the use of new-generation CARs such as TRUCKs or bi-specific CARs, the combination of CAR therapy with chemo- or radiotherapy, the use of checkpoint inhibitors, and the use of oncolytic viruses. Furthermore, despite the scarcity of targets, a growing number of phase I/II clinical trials are exploring new solid-tumor-associated antigens. Most of these antigens are of a protein nature; however, there is a clear potential in identifying carbohydrate-type antigens associated with tumors, or carbohydrate and proteoglycan antigens that emerge because of aberrant glycosylations occurring in the context of tumor transformation. Full article
(This article belongs to the Special Issue Advancements in Cancer Immunotherapy beyond Checkpoint Blockade)
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