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

被引:25
|
作者
Maali, Amirhosein [1 ,2 ]
Gholizadeh, Monireh [1 ,3 ]
Feghhi-Najafabadi, Saba [1 ]
Noei, Ahmad [1 ]
Seyed-Motahari, Seyedeh Sheila [1 ,4 ]
Mansoori, Shafieeh [1 ]
Sharifzadeh, Zahra [1 ]
机构
[1] Pasteur Inst Iran, Dept Immunol, Tehran, Iran
[2] Qazvin Univ Med Sci, Fac Allied Med, Dept Med Biotechnol, Qazvin, Iran
[3] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Biotechnol, Tabriz, Iran
[4] Islamic Azad Univ, Dept Biol, Sci & Res Branch, Tehran, Iran
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
nanobodies; single domain antibodies; cancer immunotherapy; immune cell therapy; CAR; BiTE; BiKE; immune checkpoint; CHIMERIC ANTIGEN RECEPTOR; SINGLE-DOMAIN ANTIBODIES; CAR-T-CELLS; BISPECIFIC ANTIBODY; MEMBRANE ANTIGEN; PANCREATIC-CANCER; TARGETING PD-L1; JURKAT CELLS; ENGAGER BITE; TUMOR;
D O I
10.3389/fimmu.2023.1012841
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页数:19
相关论文
共 50 条
  • [1] Nanobodies: A Game-Changer in Cell-Mediated Immunotherapy for Cancer
    Mustafa, Mujahed I.
    Mohammed, Ahmed
    SLAS DISCOVERY, 2023, 28 (08) : 358 - 364
  • [2] Molecular imaging of cell-mediated cancer immunotherapy
    Lucignani, Giovanni
    Ottobrini, Luisa
    Martelli, Cristina
    Rescigno, Maria
    Clerici, Mario
    TRENDS IN BIOTECHNOLOGY, 2006, 24 (09) : 410 - 418
  • [3] STRATEGIES FOR CELL-MEDIATED IMMUNOTHERAPY OF CANCER - KILLING OR HELP
    FORNI, G
    GIOVARELLI, M
    IMMUNOLOGY TODAY, 1986, 7 (7-8): : 202 - 203
  • [4] Biomaterials Facilitating Dendritic Cell-Mediated Cancer Immunotherapy
    Dong, Heng
    Li, Qiang
    Zhang, Yu
    Ding, Meng
    Teng, Zhaogang
    Mou, Yongbin
    ADVANCED SCIENCE, 2023, 10 (18)
  • [5] A novel cell-mediated immunotherapy for treatment of lung and breast cancer
    Venugopal, Indu
    Gormley, Claire
    McGuire, Michael J.
    Brown, Kathlynn C.
    MOLECULAR CANCER THERAPEUTICS, 2019, 18 (12)
  • [6] microRNAs Shape Myeloid Cell-Mediated Resistance to Cancer Immunotherapy
    Daveri, Elena
    Vergani, Elisabetta
    Shahaj, Eriomina
    Bergamaschi, Laura
    La Magra, Stefano
    Dosi, Michela
    Castelli, Chiara
    Rodolfo, Monica
    Rivoltini, Licia
    Vallacchi, Viviana
    Huber, Veronica
    FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [7] Personalized T cell-mediated cancer immunotherapy: progress and challenges
    Bethune, Michael T.
    Joglekar, Alok V.
    CURRENT OPINION IN BIOTECHNOLOGY, 2017, 48 : 142 - 152
  • [8] CELL-MEDIATED CYTOTOXICITY AND IMMUNOTHERAPY CHEMOTHERAPY IN CANCER-TREATMENT
    DEFILIPPI, R
    BONFINI, TD
    RICCI, F
    NUNZIATA, C
    FUGGETTA, MP
    SCARSI, A
    DEVECCHIS, L
    BONMASSAR, E
    MICROBIOLOGICAL, CHEMOTHERAPEUTICAL AND IMMUNOLOGICAL PROBLEMS IN HIGH RISK PATIENTS, 1989, 61 : 55 - 62
  • [9] Putting the brakes on BTLA in T cell-mediated cancer immunotherapy
    Paulos, Chrystal M.
    June, Carl H.
    JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (01): : 76 - 80
  • [10] Dendritic cell-mediated cancer immunotherapy with Ecklonia cava fucoidan
    Park, Hae-Bin
    Hwang, Juyoung
    Lim, Seong-Min
    Zhang, Wei
    Jin, Jun-O
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 159 : 941 - 947