Recent advances in mRNA cancer vaccines: meeting challenges and embracing opportunities

被引:73
作者
Wang, Bolin [1 ,2 ,4 ]
Pei, Jinli [2 ,4 ]
Xu, Shengnan [2 ,4 ]
Liu, Jie [2 ,3 ,4 ]
Yu, Jinming [2 ,3 ,4 ]
机构
[1] Sichuan Univ, West China Hosp, Lung Canc Ctr, Chengdu, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Dept Radiat Oncol, Shandong Canc Hosp & Inst, Jinan, Shandong, Peoples R China
[3] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp Inst, Shandong Prov Key Lab Radiat Oncol, Jinan, Shandong, Peoples R China
[4] Chinese Acad Med Sci, Res Unit Radiat Oncol, Jinan, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
mRNA cancer vaccines; cancer; cancer vaccine; personalized vaccine; cancer therapy; immunotherapy; IMMUNE-RESPONSES; GENE-TRANSFER; CELLS; ANTIGENS; IMMUNOTHERAPY; HETEROGENEITY; ELISPOT;
D O I
10.3389/fimmu.2023.1246682
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since the successful application of messenger RNA (mRNA) vaccines in preventing COVID-19, researchers have been striving to develop mRNA vaccines for clinical use, including those exploited for anti-tumor therapy. mRNA cancer vaccines have emerged as a promising novel approach to cancer immunotherapy, offering high specificity, better efficacy, and fewer side effects compared to traditional treatments. Multiple therapeutic mRNA cancer vaccines are being evaluated in preclinical and clinical trials, with promising early-phase results. However, the development of these vaccines faces various challenges, such as tumor heterogeneity, an immunosuppressive tumor microenvironment, and practical obstacles like vaccine administration methods and evaluation systems for clinical application. To address these challenges, we highlight recent advances from preclinical studies and clinical trials that provide insight into identifying obstacles associated with mRNA cancer vaccines and discuss potential strategies to overcome them. In the future, it is crucial to approach the development of mRNA cancer vaccines with caution and diligence while promoting innovation to overcome existing barriers. A delicate balance between opportunities and challenges will help guide the progress of this promising field towards its full potential.
引用
收藏
页数:15
相关论文
共 101 条
[1]   Genetic variegation of clonal architecture and propagating cells in leukaemia [J].
Anderson, Kristina ;
Lutz, Christoph ;
van Delft, Frederik W. ;
Bateman, Caroline M. ;
Guo, Yanping ;
Colman, Susan M. ;
Kempski, Helena ;
Moorman, Anthony V. ;
Titley, Ian ;
Swansbury, John ;
Kearney, Lyndal ;
Enver, Tariq ;
Greaves, Mel .
NATURE, 2011, 469 (7330) :356-+
[2]   Strong Immune Responses Induced by Direct Local Injections of Modified mRNA-Lipid Nanocomplexes [J].
Arya, Smriti ;
Lin, Qiubin ;
Zhou, Nan ;
Gao, Xiang ;
Huang, Jian-Dong .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2020, 19 :1098-1109
[3]   Intravenous nanoparticle vaccination generates stem-like TCF1+ neoantigen-specific CD8+ T cells [J].
Baharom, Faezzah ;
Ramirez-Valdez, Ramiro A. ;
Tobin, Kennedy K. S. ;
Yamane, Hidehiro ;
Dutertre, Charles-Antoine ;
Khalilnezhad, Ahad ;
Reynoso, Glennys, V ;
Coble, Vincent L. ;
Lynn, Geoffrey M. ;
Mule, Matthew P. ;
Martins, Andrew J. ;
Finnigan, John P. ;
Zhang, Xiao Meng ;
Hamerman, Jessica A. ;
Bhardwaj, Nina ;
Tsang, John S. ;
Hickman, Heather D. ;
Ginhoux, Florent ;
Ishizuka, Andrew S. ;
Seder, Robert A. .
NATURE IMMUNOLOGY, 2021, 22 (01) :41-52
[4]  
Balachandran VP, 2022, J CLIN ONCOL, V40
[5]   The clinical progress of mRNA vaccines and immunotherapies [J].
Barbier, Ann J. ;
Jiang, Allen Yujie ;
Zhang, Peng ;
Wooster, Richard ;
Anderson, Daniel G. .
NATURE BIOTECHNOLOGY, 2022, 40 (06) :840-854
[6]   Abscopal effects of radiotherapy and combined mRNA-based immunotherapy in a syngeneic, OVA-expressing thymoma mouse model [J].
Basler, Lucas ;
Kowalczyk, Aleksandra ;
Heidenreich, Regina ;
Fotin-Mleczek, Mariola ;
Tsitsekidis, Savas ;
Zips, Daniel ;
Eckert, Franziska ;
Huber, Stephan M. .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2018, 67 (04) :653-662
[7]   mRNA therapeutics in cancer immunotherapy [J].
Beck, Jan D. ;
Reidenbach, Daniel ;
Salomon, Nadja ;
Sahin, Ugur ;
Tureci, Ozlem ;
Vormehr, Mathias ;
Kranz, Lena M. .
MOLECULAR CANCER, 2021, 20 (01)
[8]   Tumour heterogeneity in the clinic [J].
Bedard, Philippe L. ;
Hansen, Aaron R. ;
Ratain, Mark J. ;
Siu, Lillian L. .
NATURE, 2013, 501 (7467) :355-364
[9]   mRNA-LNP vaccines tuned for systemic immunization induce strong antitumor immunity by engaging splenic immune cells [J].
Bevers, Sanne ;
Kooijmans, Sander A. A. ;
Van de Velde, Elien ;
Evers, Martijn J. W. ;
Seghers, Sofie ;
Gitz-Francois, Jerney J. J. M. ;
van Kronenburg, Nicky C. H. ;
Fens, Marcel H. A. M. ;
Mastrobattista, Enrico ;
Hassler, Lucie ;
Sork, Helena ;
Lehto, Taavi ;
Ahmed, Kariem E. ;
El Andaloussi, Samir ;
Fiedler, Katja ;
Breckpot, Karine ;
Maes, Michael ;
Van Hoorick, Diane ;
Bastogne, Thierry ;
Schiffelers, Raymond M. ;
De Koker, Stefaan .
MOLECULAR THERAPY, 2022, 30 (09) :3078-3094
[10]   A TCR-like CAR Promotes Sensitive Antigen Recognition and Controlled T-cell Expansion Upon mRNA Vaccination [J].
Birtel, Matthias ;
Voss, Ralf-Holger ;
Reinhard, Katharina ;
Rengstl, Benjamin ;
Ouchan, Yasmina ;
Michel, Kristina ;
Hayduk, Nina ;
Tillmann, Bodo ;
Becker, Rene ;
Suchan, Martin ;
Theobald, Matthias ;
Oehm, Petra ;
Tuereci, Oezlem ;
Sahin, Ugur .
CANCER RESEARCH COMMUNICATIONS, 2022, 2 (08) :827-841