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Nanobodies in cell-mediated immunotherapy: On the road to fight cancer

The immune system is essential in recognizing and eliminating tumor cells. The unique characteristics of the tumor microenvironment (TME), such as heterogeneity, reduced blood flow, hypoxia, and acidity, can reduce the efficacy of cell-mediated immunity. The primary goal of cancer immunotherapy is t...

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Autores principales: Maali, Amirhosein, Gholizadeh, Monireh, Feghhi-Najafabadi, Saba, Noei, Ahmad, Seyed-Motahari, Seyedeh Sheila, Mansoori, Shafieeh, Sharifzadeh, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905824/
https://www.ncbi.nlm.nih.gov/pubmed/36761751
http://dx.doi.org/10.3389/fimmu.2023.1012841
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author Maali, Amirhosein
Gholizadeh, Monireh
Feghhi-Najafabadi, Saba
Noei, Ahmad
Seyed-Motahari, Seyedeh Sheila
Mansoori, Shafieeh
Sharifzadeh, Zahra
author_facet Maali, Amirhosein
Gholizadeh, Monireh
Feghhi-Najafabadi, Saba
Noei, Ahmad
Seyed-Motahari, Seyedeh Sheila
Mansoori, Shafieeh
Sharifzadeh, Zahra
author_sort Maali, Amirhosein
collection PubMed
description The immune system is essential in recognizing and eliminating tumor cells. The unique characteristics of the tumor microenvironment (TME), such as heterogeneity, reduced blood flow, hypoxia, and acidity, can reduce the efficacy of cell-mediated immunity. The primary goal of cancer immunotherapy is to modify the immune cells or the TME to enable the immune system to eliminate malignancies successfully. Nanobodies, known as single-domain antibodies, are light chain-free antibody fragments produced from Camelidae antibodies. The unique properties of nanobodies, including high stability, reduced immunogenicity, enhanced infiltration into the TME of solid tumors and facile genetic engineering have led to their promising application in cell-mediated immunotherapy. They can promote the cancer therapy either directly by bridging between tumor cells and immune cells and by targeting cancer cells using immune cell-bound nanobodies or indirectly by blocking the inhibitory ligands/receptors. The T-cell activation can be engaged through anti-CD3 and anti-4-1BB nanobodies in the bispecific (bispecific T-cell engagers (BiTEs)) and trispecific (trispecific T-cell engager (TriTEs)) manners. Also, nanobodies can be used as natural killer (NK) cell engagers (BiKEs, TriKEs, and TetraKEs) to create an immune synapse between the tumor and NK cells. Nanobodies can redirect immune cells to attack tumor cells through a chimeric antigen receptor (CAR) incorporating a nanobody against the target antigen. Various cancer antigens have been targeted by nanobody-based CAR-T and CAR-NK cells for treating both hematological and solid malignancies. They can also cause the continuation of immune surveillance against tumor cells by stopping inappropriate inhibition of immune checkpoints. Other roles of nanobodies in cell-mediated cancer immunotherapy include reprogramming macrophages to reduce metastasis and angiogenesis, as well as preventing the severe side effects occurring in cell-mediated immunotherapy. Here, we highlight the critical functions of various immune cells, including T cells, NK cells, and macrophages in the TME, and discuss newly developed immunotherapy methods based on the targeted manipulation of immune cells and TME with nanobodies.
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spelling pubmed-99058242023-02-08 Nanobodies in cell-mediated immunotherapy: On the road to fight cancer Maali, Amirhosein Gholizadeh, Monireh Feghhi-Najafabadi, Saba Noei, Ahmad Seyed-Motahari, Seyedeh Sheila Mansoori, Shafieeh Sharifzadeh, Zahra Front Immunol Immunology The immune system is essential in recognizing and eliminating tumor cells. The unique characteristics of the tumor microenvironment (TME), such as heterogeneity, reduced blood flow, hypoxia, and acidity, can reduce the efficacy of cell-mediated immunity. The primary goal of cancer immunotherapy is to modify the immune cells or the TME to enable the immune system to eliminate malignancies successfully. Nanobodies, known as single-domain antibodies, are light chain-free antibody fragments produced from Camelidae antibodies. The unique properties of nanobodies, including high stability, reduced immunogenicity, enhanced infiltration into the TME of solid tumors and facile genetic engineering have led to their promising application in cell-mediated immunotherapy. They can promote the cancer therapy either directly by bridging between tumor cells and immune cells and by targeting cancer cells using immune cell-bound nanobodies or indirectly by blocking the inhibitory ligands/receptors. The T-cell activation can be engaged through anti-CD3 and anti-4-1BB nanobodies in the bispecific (bispecific T-cell engagers (BiTEs)) and trispecific (trispecific T-cell engager (TriTEs)) manners. Also, nanobodies can be used as natural killer (NK) cell engagers (BiKEs, TriKEs, and TetraKEs) to create an immune synapse between the tumor and NK cells. Nanobodies can redirect immune cells to attack tumor cells through a chimeric antigen receptor (CAR) incorporating a nanobody against the target antigen. Various cancer antigens have been targeted by nanobody-based CAR-T and CAR-NK cells for treating both hematological and solid malignancies. They can also cause the continuation of immune surveillance against tumor cells by stopping inappropriate inhibition of immune checkpoints. Other roles of nanobodies in cell-mediated cancer immunotherapy include reprogramming macrophages to reduce metastasis and angiogenesis, as well as preventing the severe side effects occurring in cell-mediated immunotherapy. Here, we highlight the critical functions of various immune cells, including T cells, NK cells, and macrophages in the TME, and discuss newly developed immunotherapy methods based on the targeted manipulation of immune cells and TME with nanobodies. Frontiers Media S.A. 2023-01-25 /pmc/articles/PMC9905824/ /pubmed/36761751 http://dx.doi.org/10.3389/fimmu.2023.1012841 Text en Copyright © 2023 Maali, Gholizadeh, Feghhi-Najafabadi, Noei, Seyed-Motahari, Mansoori and Sharifzadeh https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Immunology
Maali, Amirhosein
Gholizadeh, Monireh
Feghhi-Najafabadi, Saba
Noei, Ahmad
Seyed-Motahari, Seyedeh Sheila
Mansoori, Shafieeh
Sharifzadeh, Zahra
Nanobodies in cell-mediated immunotherapy: On the road to fight cancer
title Nanobodies in cell-mediated immunotherapy: On the road to fight cancer
title_full Nanobodies in cell-mediated immunotherapy: On the road to fight cancer
title_fullStr Nanobodies in cell-mediated immunotherapy: On the road to fight cancer
title_full_unstemmed Nanobodies in cell-mediated immunotherapy: On the road to fight cancer
title_short Nanobodies in cell-mediated immunotherapy: On the road to fight cancer
title_sort nanobodies in cell-mediated immunotherapy: on the road to fight cancer
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905824/
https://www.ncbi.nlm.nih.gov/pubmed/36761751
http://dx.doi.org/10.3389/fimmu.2023.1012841
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