Simultaneous, cell-intrinsic downregulation of PD-1 and TIGIT enhances the effector function of CD19-targeting CAR T cells and promotes an early-memory phenotype

التفاصيل البيبلوغرافية
العنوان: Simultaneous, cell-intrinsic downregulation of PD-1 and TIGIT enhances the effector function of CD19-targeting CAR T cells and promotes an early-memory phenotype
المؤلفون: Seok Jin Kim, Yujean Lee, Oded Singer, Xinxin Wang, Won Seog Kim, Young-Ho Lee, Su Kyung Nam, Hyeong Ji Lee, Chan Hyuk Kim, Hyung Cheol Kim, Youngil Koh, Inkyung Jung, Cedric Hupperetz, Jennifer S. Y. Ma
بيانات النشر: Cold Spring Harbor Laboratory, 2020.
سنة النشر: 2020
مصطلحات موضوعية: LAG3, biology, Chemistry, Chimeric antigen receptor, Immune checkpoint, CD19, medicine.anatomical_structure, TIGIT, Downregulation and upregulation, Antigen, medicine, Cancer research, biology.protein, B cell
الوصف: CD19-targeting chimeric antigen receptor (CAR) T cells have become an important therapeutic option for patients with relapsed and refractory B cell malignancies. However, recent clinical data indicate that a significant portion of patients still do not benefit from the therapy owing to various resistance mechanisms, including high expression of multiple inhibitory immune checkpoint receptors on activated CAR T cells. Here, we report a lentiviral two-in-one CAR T approach in which two checkpoint receptors are downregulated simultaneously by a dual short-hairpin RNA (shRNA) cassette integrated into a CAR vector. Using this system, we evaluated CD19-targeting CAR T cells in the context of four different checkpoint combinations—PD-1/TIM-3, PD-1/LAG-3, PD-1/CTLA-4 and PD-1/TIGIT—and found that CAR T cells with PD-1/TIGIT downregulation uniquely exerted synergistic antitumor effects in mouse xenograft models compared with PD-1 single downregulation, and maintained cytolytic and proliferative capacity upon repeated antigen exposure. Importantly, functional and phenotypic analyses of CAR T cells as well as analyses of transcriptomic profiles suggested that downregulation of PD-1 enhances short-term effector function, whereas downregulation of TIGIT is primarily responsible for maintaining a less-differentiated/exhausted state, providing a potential mechanism for the observed synergy. The PD-1/TIGIT–downregulated CAR T cells generated from diffuse large B-cell lymphoma patient-derived T cells using a clinically applicable manufacturing process also showed robust antitumor activity and significantly improved persistence in vivo compared with conventional CD19-targeting CAR T cells. Overall, our results demonstrate that the cell-intrinsic PD-1/TIGIT dual downregulation strategy may prove effective in overcoming immune checkpoint-mediated resistance in CAR T therapy.
DOI: 10.1101/2020.11.07.372334
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::696d445b016ce35b1d47e02fb9738d8d
https://doi.org/10.1101/2020.11.07.372334
Rights: OPEN
رقم الانضمام: edsair.doi...........696d445b016ce35b1d47e02fb9738d8d
قاعدة البيانات: OpenAIRE
الوصف
DOI:10.1101/2020.11.07.372334