A comparison of chimeric antigen receptors containing CD28 versus 4-1BB costimulatory domains

KM Cappell, JN Kochenderfer - Nature reviews Clinical oncology, 2021 - nature.com
Chimeric antigen receptors (CARs) are engineered proteins designed to target T cells to
cancer cells. To effectively activate the T cells in which they are expressed, CARs must …

Dendritic cells in cancer immunology and immunotherapy

SK Wculek, FJ Cueto, AM Mujal, I Melero… - Nature Reviews …, 2020 - nature.com
Dendritic cells (DCs) are a diverse group of specialized antigen-presenting cells with key
roles in the initiation and regulation of innate and adaptive immune responses. As such …

A genome-scale screen for synthetic drivers of T cell proliferation

M Legut, Z Gajic, M Guarino, Z Daniloski, JA Rahman… - Nature, 2022 - nature.com
The engineering of autologous patient T cells for adoptive cell therapies has revolutionized
the treatment of several types of cancer. However, further improvements are needed to …

Fundamental mechanisms of immune checkpoint blockade therapy

SC Wei, CR Duffy, JP Allison - Cancer discovery, 2018 - AACR
Immune checkpoint blockade is able to induce durable responses across multiple types of
cancer, which has enabled the oncology community to begin to envision potentially curative …

Immunotherapy targeting 4-1BB: mechanistic rationale, clinical results, and future strategies

C Chester, MF Sanmamed, J Wang… - Blood, The Journal of …, 2018 - ashpublications.org
4-1BB (CD137, tumor necrosis factor receptor superfamily 9) is an inducible costimulatory
receptor expressed on activated T and natural killer (NK) cells. 4-1BB ligation on T cells …

Selecting costimulatory domains for chimeric antigen receptors: functional and clinical considerations

R Weinkove, P George, N Dasyam… - Clinical & translational …, 2019 - Wiley Online Library
Costimulatory signals are required to achieve robust chimeric antigen receptor (CAR) T cell
expansion, function, persistence and antitumor activity. These can be provided by …

Structural design of engineered costimulation determines tumor rejection kinetics and persistence of CAR T cells

Z Zhao, M Condomines, SJC van der Stegen, F Perna… - Cancer cell, 2015 - cell.com
T cell engineering is a powerful means to rapidly generate anti-tumor T cells. The
costimulatory properties of second-generation chimeric antigen receptors (CARs) determine …

The pharmacology of second-generation chimeric antigen receptors

SJC Van Der Stegen, M Hamieh… - Nature reviews Drug …, 2015 - nature.com
Second-generation chimeric antigen receptors (CARs) retarget and reprogramme T cells to
augment their antitumour efficacy. The combined activating and co-stimulatory domains …

Tumor-targeted 4-1BB agonists for combination with T cell bispecific antibodies as off-the-shelf therapy

C Claus, C Ferrara, W Xu, J Sam, S Lang… - Science translational …, 2019 - science.org
Endogenous costimulatory molecules on T cells such as 4-1BB (CD137) can be leveraged
for cancer immunotherapy. Systemic administration of agonistic anti–4-1BB antibodies …

Chimeric antigen receptor designed to prevent ubiquitination and downregulation showed durable antitumor efficacy

W Li, S Qiu, J Chen, S Jiang, W Chen, J Jiang, F Wang… - Immunity, 2020 - cell.com
Clinical evidence suggests that poor persistence of chimeric antigen receptor-T cells (CAR-
T) in patients limits therapeutic efficacy. Here, we designed a CAR with recyclable capability …