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Status |
Public on May 15, 2024 |
Title |
IL-18-secreting multi-antigen targeting CAR T-cells eliminate antigen-low myeloma in an immunocompetent mouse model [in vitro] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Multiple myeloma is a plasma cell malignancy that is currently incurable with conventional therapies. Following the success of CD19-targeted chimeric antigen receptor (CAR) T-cells in leukemia and lymphoma, CAR T-cells targeting B-cell maturation antigen (BCMA) more recently demonstrated impressive activity in relapsed and refractory myeloma patients. However, BCMA-directed therapy can fail due to low expression of BCMA on myeloma cells, suggesting that novel approaches to better address antigen-low disease may improve patient outcomes. We hypothesized that engineered secretion of the pro-inflammatory cytokine interleukin-18 (IL-18) and multi-antigen targeting could improve CAR T-cell activity against BCMA-low myeloma. In a syngeneic murine model of myeloma, CAR T-cells targeting the myeloma-associated antigens BCMA and B-cell activating factor (BAFF-R) failed to eliminate myeloma when these antigens were weakly expressed. In contrast, IL-18-secreting CAR T-cells targeting these antigens promoted myeloma clearance. IL-18-secreting CAR T-cells developed an effector-like T-cell phenotype, promoted interferon-gamma production, reprogrammed the myeloma bone marrow microenvironment through type I and II interferon signaling, and utilized macrophages to mediate anti-myeloma activity. Simultaneous targeting of weakly expressed BCMA and BAFF-R with dual-CAR T-cells enhanced T-cell:target cell avidity, increased overall CAR signal strength, and stimulated anti-myeloma activity. Dual-antigen targeting augmented CAR T-cell secretion of engineered IL-18 and facilitated elimination of larger myeloma burdens in vivo. Our results demonstrate that combination of engineered IL-18 secretion and multi-antigen targeting can eliminate myeloma with weak antigen expression through distinct mechanisms.
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Overall design |
scRNA of APRIL CAR T cells +/- engineered IL-18 secretion following stimulation with MOPC315.BM.
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Web link |
https://www.sciencedirect.com/science/article/pii/S0006497124009376?via%3Dihub
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Contributor(s) |
Ng BD, Rajagopalan A, Kousa AI, Fischman JS, Chen S, Massa A, Manuele D, Elias HK, Galiano M, Lemarquis AL, Boardman AP, DeWolf S, Pierce J, Bogen B, James SE, van den Brink MM |
Citation(s) |
38579288 |
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Submission date |
Mar 18, 2024 |
Last update date |
May 15, 2024 |
Contact name |
Brandon Ng |
E-mail(s) |
ngb@mskcc.org
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Organization name |
Memorial Sloan Kettering Cancer Center
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Department |
Immunology
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Lab |
van den Brink
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Street address |
417 E 68th Street, Z1419
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City |
New York |
State/province |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (4)
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GSM8153070 |
APRIL CAR T cells +/- IL-18 replicate 1, GEX |
GSM8153071 |
APRIL CAR T cells +/- IL-18 replicate 1, HTO |
GSM8153072 |
APRIL CAR T cells +/- IL-18 replicate 2, GEX |
GSM8153073 |
APRIL CAR T cells +/- IL-18 replicate 2, HTO |
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Relations |
BioProject |
PRJNA1089207 |
Supplementary file |
Size |
Download |
File type/resource |
GSE261852_APRIL_28_18_spl1_sample_filtered_feature_bc_matrix.h5 |
15.4 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_28_18_spl2_sample_filtered_feature_bc_matrix.h5 |
9.2 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_28_spl1_sample_filtered_feature_bc_matrix.h5 |
11.6 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_28_spl2_sample_filtered_feature_bc_matrix.h5 |
8.5 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_BB_18_spl1_sample_filtered_feature_bc_matrix.h5 |
12.3 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_BB_18_spl2_sample_filtered_feature_bc_matrix.h5 |
7.8 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_BB_spl1_sample_filtered_feature_bc_matrix.h5 |
1.9 Mb |
(ftp)(http) |
H5 |
GSE261852_APRIL_BB_spl2_sample_filtered_feature_bc_matrix.h5 |
8.6 Mb |
(ftp)(http) |
H5 |
GSE261852_CI82_spl1_filtered_barcodes.tsv.gz |
72.6 Kb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl1_filtered_feature_bc_matrix.h5 |
52.1 Mb |
(ftp)(http) |
H5 |
GSE261852_CI82_spl1_filtered_features.tsv.gz |
284.1 Kb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl1_filtered_matrix.mtx.gz |
137.9 Mb |
(ftp)(http) |
MTX |
GSE261852_CI82_spl1_raw_barcodes.tsv.gz |
6.6 Mb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl1_raw_feature_bc_matrix.h5 |
89.8 Mb |
(ftp)(http) |
H5 |
GSE261852_CI82_spl1_raw_features.tsv.gz |
254.1 Kb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl1_raw_matrix.mtx.gz |
207.1 Mb |
(ftp)(http) |
MTX |
GSE261852_CI82_spl2_filtered_barcodes.tsv.gz |
58.6 Kb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl2_filtered_feature_bc_matrix.h5 |
41.3 Mb |
(ftp)(http) |
H5 |
GSE261852_CI82_spl2_filtered_features.tsv.gz |
284.1 Kb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl2_filtered_matrix.mtx.gz |
109.0 Mb |
(ftp)(http) |
MTX |
GSE261852_CI82_spl2_raw_barcodes.tsv.gz |
6.0 Mb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl2_raw_feature_bc_matrix.h5 |
70.6 Mb |
(ftp)(http) |
H5 |
GSE261852_CI82_spl2_raw_features.tsv.gz |
254.1 Kb |
(ftp)(http) |
TSV |
GSE261852_CI82_spl2_raw_matrix.mtx.gz |
160.1 Mb |
(ftp)(http) |
MTX |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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