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identifier: SDY1108
description:
A systems approach reveals that engagement of systemic immunity is critical to the process of tumor rejection following immunotherapy. Using a spontaneous model of triple-negative breast cancer, we assessed immune cell dynamics across the organism during tumor rejection
aggregation:
instance of dataset
refinement:
2 - Complete set of descriptive data and results, as ascertained by ImmPort.
availability:
available with registration
primaryPublications: 28111070
isAbout:
By using mass CyTOF to systematically characterizing diverse cell subsets and their activation states simultaneously under different treatment conitions in a spontaneous mouse model of triple-negative breast cancer. To assess immune cell dynamics across the organism during tumor rejection, the lab developed intuitive models for visualizing single-cell data with statistical inference. To conduct validations on the hypothesis generated from the global analysis results.
clinical trial:
study category: Oncology
study type: Interventional
subject species: Mus musculus
biosample type: Bone Marrow
Lymph node
Other
Spleen
Whole blood
subject gender: Both
assay type: CyTOF
name:
cancer immunotherapy
fullName:
Matthew Spitzer
Garry Nolan
Edgar Engleman
affiliations:
UCSF+Stanford University
Stanford University
roles:
principal investigator
name:
Systemic Immunity for Cancer Immunotherapy
size:
13
output:
Mass CyTOF, Scaffold maps, Cell population profiles in MMTV models, BP melanoma models, and metastatic melanoma patients on clinical trial, Adoptive T Cell Transfer study, and Statistical Scaffold in R. The highlighted results: System-wide models reveal coordinated anti-tumor immunity across the organism, Tumor eradication requires immune activation in the periphery, Network analysis identifies CD4 T cells sufficient to initiate immune responses, PD-L1 upregulation early post-therapy protects distal tumors from systemic immunity
studyGroups:
MMTV_UnTreated_Day3: no treatment to MMTV mice,a spontaneous model of triple-negative breast cancer, sample collected at day3
MMTV_UnTreated_Day8: no treatment to MMTV mice, sample collected at day8 (matched to treatment group)
MMTV_B6Antibodies_Day3: effective tumor-binding antibody therapy, B6-alloIgG + anti-CD40 + IFNg, priming phase
MMTV_B6Antibodies_Day8: effective tumor-binding antibody therapy, B6-alloIgG + anti-CD40 + IFNg, rejection phase
MMTV_CD1Antibodies_Day3: effective tumor-binding antibody therapy, CD-1-alloIgG + anti-CD40 + IFNg, priming phase
MMTV_CD1Antibodies_Day8: effective tumor-binding antibody therapy, CD-1-alloIgG + anti-CD40 + IFNg, rejection phase
MMTV_antiPD1_Day3: ineffective therapy, anti-PD-1, priming phase
MMTV_antiPD1_Day8: ineffective therapy, anti-PD-1, rejection phase
MMTV_CD4_Tcell_transfer: therapy of effective CD4 T cells transfer to naive MMTV mice, time series assay
BP_ineffective: ineffctive therapy in the inducible mouse model of melanoma driven by Braf^V600E and loss of Pten
BP_effective: effective therapy in the inducible mouse model of melanoma driven by Braf^V600E and loss of Pten
MMTV_vehicle: vehicle control to MMTV mice with multi-focal disease after tumor-binding antibody therapy
MMTV_antiPD-L1: antiPD-L1 therapy combined with tumor-binding antibody therapy to MMTV mice with multi-focal disease
hum_responder: metastatic melanoma patients responded to the therapy of anti-CTLA-4 antibodies (Ipilimumab) in combination with GM-CSF
hum_non-responders: metastatic melanoma patients patients did not respond to the therapy of anti-CTLA-4 antibodies (Ipilimumab) in combination with GM-CSF
description:
A systems approach reveals that engagement of systemic immunity is critical to the process of tumor rejection following immunotherapy. Using a spontaneous model of triple-negative breast cancer, we assessed immune cell dynamics across the organism during tumor rejection
identifier:
10.21430/M3L410EFMQ
startDate:
2015-01-01
name:
ImmPort
identifier:
SCR:012804
homePage: http://www.immport.org