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Series GSE215086 Query DataSets for GSE215086
Status Public on Oct 12, 2022
Title Knocking out BATF improves CAR-T cell efficacy by resisting exhaustion and forming central memory cells
Organisms Homo sapiens; Mus musculus
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary Chimeric antigen receptor modified T (CAR-T) cell therapy has limited efficacy against solid tumor, one major challenge is T cell exhaustion. To address this challenge, we performed a candidate gene screen using a hypofunction CAR-T cell model, and found that knocking out BATF improved the performance of CAR-T cells. In different types of CAR-T cells and mouse OT-1 cells, knocking out BATF endows T cells with improved resistance to exhaustion and better tumor eradication efficacy. We find that BATF binds to and up-regulates a subset of exhaustion genes in human CAR-T cells. Furthermore, BATF regulates the expression of genes involved in the development of effector and memory cells, and knocking out BATF shifts the population towards more central memory subset. Therefore, we conclude that BATF is a key factor limiting CAR-T cell function, and its depletion improves CAR-T cells efficacy against solid tumor.
 
Overall design We established an in vitro CAR-T cell hypofunction model and identify that BATF drives exhaustion via binding to and upregulating related genes in CAR-T cells, as well as regulates CAR-T cell subtypes. Knocking out BATF improves CAR-T cells efficacy against solid tumor.

We sorted GFP-positive cells co-cultured with tumor at 0.1:1 E:T ratio at day 7, named as hypofunction M28Z. After being co-cultured with tumor cells for 24h at E: T=2:1 (achieved 90% tumor lysis), GFP-positive CAR-T cells were sorted and named as activated M28Z; CAR-T cells thawed from the cryopreserved stock were sorted as control (fresh M28Z). To further characterize these hypofunction CAR-T cells, we performed RNA-seq on CD8-positive cells isolated from these three groups mentioned above. In addition, to control for the influence of long-term cultivation on CAR-T cells, we sequenced CAR-T cells cultured alone for 7 days (named unstimulated M28Z). To investigate the role of BATF and IRF4 in CAR-T cell exhaustion, we performed RNA-seq analysis of M28Z, M28Z-BKO and IKO cells isolated from the hypofunction model. To further validate the function of BATF in human CAR-T cells, we over-expressed BATF in CAR-T cells (M28Z-BOE) by lentiviral transduction and RNA-seq was performed using M28Z, M28Z-BKO, M28Z-BOE after three rounds of tumor cell challenges. To further dissect the molecular mechanism, we performed ChIP sequencing (ChIP-seq) in M28Z CAR-T cells. To better dissect the role of Batf in primary T cells, RNA-seq was performed using OT-1 cells upon repetitive tumor challenge.
 
Contributor(s) Wang H, Zhang X, Qiao M, Zhang C
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Submission date Oct 08, 2022
Last update date Oct 14, 2022
Contact name Xingying Zhang
E-mail(s) zhangxingying@ioz.ac.cn
Phone 18811104623
Organization name Institute of Zoology, Chinese Academy of Sciences
Street address No. 5, Yard 1, Beichen West Road, Chaoyang District
City Beijing
ZIP/Postal code 100101
Country China
 
Platforms (3)
GPL20795 HiSeq X Ten (Homo sapiens)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (40)
GSM6621043 unstimulated_1
GSM6621044 unstimulated_2
GSM6621045 unstimulated_3
Relations
BioProject PRJNA888383

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Supplementary file Size Download File type/resource
GSE215086_Human_Three_rounds_tumor_challenge_readcounts_FPKM.xlsx 5.9 Mb (ftp)(http) XLSX
GSE215086_Human_lowratio_model_readcounts_FPKM.xlsx 10.0 Mb (ftp)(http) XLSX
GSE215086_Mouse_OT-1_readcounts_FPKM.xlsx 6.1 Mb (ftp)(http) XLSX
GSE215086_RAW.tar 788.2 Mb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record
Processed data provided as supplementary file

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