Department of Immunology, Pasteur Institute of Iran, Tehran, Iran.
Department of Medical Biotechnology, Faculty of Allied Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
Front Immunol. 2023 Jan 25;14:1012841. doi: 10.3389/fimmu.2023.1012841. eCollection 2023.
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.
免疫系统对于识别和消除肿瘤细胞至关重要。肿瘤微环境(TME)的独特特征,如异质性、血流减少、缺氧和酸中毒,会降低细胞介导免疫的疗效。癌症免疫疗法的主要目标是修饰免疫细胞或 TME,使免疫系统能够成功消除恶性肿瘤。纳米抗体,也称为单域抗体,是从骆驼科抗体中产生的无重链的抗体片段。纳米抗体的独特性质,包括高稳定性、低免疫原性、增强对实体瘤 TME 的渗透以及易于遗传工程,使其在细胞介导的免疫疗法中具有广阔的应用前景。它们可以通过桥接肿瘤细胞和免疫细胞,或者通过使用免疫细胞结合的纳米抗体靶向癌细胞,直接促进癌症治疗,或者通过阻断抑制性配体/受体间接促进癌症治疗。通过双特异性(双特异性 T 细胞衔接子(BiTEs)和三特异性(三特异性 T 细胞衔接子(TriTEs))和抗 CD3 和抗 4-1BB 纳米抗体可以使 T 细胞激活。此外,纳米抗体可以用作自然杀伤 (NK) 细胞衔接子(BiKEs、TriKEs 和 TetraKEs),在肿瘤和 NK 细胞之间形成免疫突触。通过将针对靶抗原的纳米抗体与嵌合抗原受体 (CAR) 结合,纳米抗体可以将免疫细胞重定向攻击肿瘤细胞。基于纳米抗体的 CAR-T 和 CAR-NK 细胞已针对血液系统恶性肿瘤和实体恶性肿瘤的各种癌症抗原进行了靶向治疗。它们还可以通过阻止免疫检查点的不当抑制来继续对肿瘤细胞进行免疫监视。纳米抗体在细胞介导的癌症免疫疗法中的其他作用包括重编程巨噬细胞以减少转移和血管生成,以及防止细胞介导的免疫疗法中出现严重的副作用。在这里,我们强调了 TME 中各种免疫细胞(包括 T 细胞、NK 细胞和巨噬细胞)的关键功能,并讨论了基于纳米抗体靶向免疫细胞和 TME 的新开发的免疫疗法方法。