|
Status |
Public on Jul 29, 2024 |
Title |
TCR-T-TIL-6 |
Sample type |
SRA |
|
|
Source name |
tumor
|
Organism |
Homo sapiens |
Characteristics |
tissue: tumor cell line: primary cells cell type: TCR-engineered human T cells genotype: NY-ESO-1 TCR expression treatment: PBS
|
Treatment protocol |
i.p. injection of PBS or orthogonal human IL-2
|
Growth protocol |
Tumor infiltrating T cells
|
Extracted molecule |
genomic DNA |
Extraction protocol |
NSG mice were inoculated s.c. with A375 cells (1 × 106) and received i.v. adoptive cell transfer of 3 × 106 NY-ESO-1 TCR-T cells (WT NY-ESO-1 TCR-T cells, or ho22R, or hoGCSFR expressing NY-ESO-1 TCR-T cells) on day 10 post-tumor inoculation followed by i.p. administration of MSA-hoIL-2 (2.5 × 104 unit × 3 doses, 2.5 × 104 unit × 3 doses) or PBS control every other day until day 20. On day 21, mice were sacrificed, tumors were minced and dissociated using a human tumor dissociation kit (Miltenyi Biotec) and a gentleMACS Octo Dissociator (Miltenyi Biotec). Tumor-infiltrating lymphocytes (TILs) were first enriched by density gradient centrifugation against Percoll (GE healthcare), and then stained with surface markers and DAPI (Sigma-Aldrich). CD3+ EGFR+ or CD3+ EGFR+YFP+ T cells were sorted using an Aria II sorter (BD Biosciences) at the Stanford Share FACS Facility for ATAC sequencing ATAC-seq library was generateded using Active Motif ATAC-Seq Kit
|
|
|
Library strategy |
ATAC-seq |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina NovaSeq X |
|
|
Description |
Omni-ATAC-seq
|
Data processing |
ATAC-seq reads were mapped onto the reference genome (hg19) using RSubread (version 2.18.0) in the “DNA” mode The aligned reads were then subjected to peak calling with MACS3 Assembly: hg19 Supplementary files format and content: ATACSeq_DESeq2_rsubread.rds, summarized peak count data
|
|
|
Submission date |
Jul 16, 2024 |
Last update date |
Jul 29, 2024 |
Contact name |
Yang Zhao |
E-mail(s) |
yannzhao@stanford.edu
|
Phone |
6505058145
|
Organization name |
Stanford University
|
Department |
MCP
|
Lab |
Garcia lab
|
Street address |
Beckman B169B, 279 Campus Drive
|
City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
|
|
Platform ID |
GPL34281 |
Series (1) |
GSE272385 |
Natural and non-natural cytokine receptors generate diverse cell states to enhance T cell therapy |
|
Relations |
BioSample |
SAMN42537151 |
SRA |
SRX25346687 |