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Links from GEO DataSets

Items: 20

1.

RNA expression of memory NK subsets

(Submitter supplied) we compared and reported RNA expression difference in memory and non-memory NK cell subsets
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: XLS
Series
Accession:
GSE124321
ID:
200124321
2.

Expression data from WT and Klrc1-/- CD8+ T cells

(Submitter supplied) CD8+ T cells and NK cells protect from viral infections by killing virally-infected cells and secreting interferon-g. Several inhibitory receptors limit the magnitude and duration of these anti-viral responses. We used microarrays to assess the transcriptome of ectromelia virus (ECTV) specific CD8+ T cells that genetically lack one such receptor, NKG2A, which is encoded by Klrc1.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
15 Samples
Download data: CEL, TXT
Series
Accession:
GSE74780
ID:
200074780
3.

Expression arrays of inflammatory Ly6C+ monocytes in mice primary or secondary challenged with Listeria monocytogenes

(Submitter supplied) In this study we investigated the mechanisms involved in memory T-cell mediated protection using mice vaccinated with the intracellular bacterium Listeria monocytogenes. Our working hypothesis was that rapid activation of cells of the innate immune system, in particular inflammatory Ly6C+ monocytes, were essential in effective protection, in a memory T cell-dependent manner. Thus we generated a comprehensive comparison of the genetic program of activated Ly6C+ monocytes during a primary or a secondary infection with Listeria monocytogenes, at 8 hours post challenge infection. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE58014
ID:
200058014
4.

Exploration of human lung resident immunity and response to respiratory viral infection in a humanized mouse model

(Submitter supplied) There is an urgent need for humanized mouse models of viral respiratory diseases to study immunopathogenesis and therapeutic interventions. Although mice with a functional human immune system (HIS) permit analysis in real time of human immune responses in vivo, evolutionary divergences preclude their usefulness for studies of respiratory viruses that do not infect mouse lungs. Here, we sought to use HIS mice with human lung tissue xenografts (referred to as HISL mice) to address this issue. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
2 Samples
Download data: TXT
Series
Accession:
GSE152563
ID:
200152563
5.

Expression data from primary and secondary CD4 T cell effectors responding towards influenza A virus infection

(Submitter supplied) How secondary CD4 T cell effectors, derived from resting memory cells, differ from primary cells, derived from naïve precursors, and how such differences impact recall responses to pathogens is unknown. We used microarrays to detail the global programme of gene expression underlying differences between primary and secondary CD4 T cell effectors purified from the spleen, dLN, and lung on day 7 following A/PR8/34 influenza infection.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
15 Samples
Download data: CEL
Series
Accession:
GSE40230
ID:
200040230
6.

Multi-tissue Single-Cell Analysis Deconstructs the Complexities of Mouse NK-ILC1 Programs

(Submitter supplied) Natural killer (NK) cells and type 1 innate lymphoid cells (ILC1s) are a heterogenous group of T-bet+ innate cells that produce IFN-γ and are broadly defined as lineage–NK1.1+NKp46+ cells in mice. ILC1s definition primarily stems from studies on liver-resident and small intestinal populations. However, ILC1s in many anatomical sites, including visceral adipose tissue, salivary glands, and uterus, exhibit non-uniform programs that do not adequately overlap with those of liver or gut ILC1s or NK cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
130 Samples
Download data: TXT
Series
Accession:
GSE158547
ID:
200158547
7.

Lung dendritic cells migrate to the spleen to prime long-lived memory CD8+ T cell precursors after influenza virus infection

(Submitter supplied) CD8+ T cell responses to pulmonary challenges are primed by lung-migratory dendritic cells (mDCs), which capture antigens in the lung and migrate to the lung-draining mediastinal lymph node (med-LNs) to activate T cells. Notably, the lung and the spleen are not connected by the lymphatic vasculature. Thus, the current paradigm suggests that the med-LN is the only site for T cell priming to viruses that are restricted to the respiratory tract. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
9 Samples
Download data: TXT
Series
Accession:
GSE179995
ID:
200179995
8.

The PD-1 pathway regulates development and function of memory CD8+ T cells following respiratory viral infection

(Submitter supplied) The PD-1:PD-L co-inhibitory pathway regulates dysfunctional T cells in chronic viral infection and cancer, but the role of this pathway in effector and memory responses following acute infection or vaccination remains less clear. Here we demonstrated that in the absence of signals from the PD-1 pathway, cell intrinsic alterations during initial CD8+ T cell priming resulted in excessive early CD8+ T cell expansion, but increased CD8+ T cell contraction and aberrant effector to memory CD8+ T cell transition. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8321
12 Samples
Download data: CEL
Series
Accession:
GSE149425
ID:
200149425
9.

Gene profiling of naive and Listeria monocytogenes-induced memory CD8 T lymphocytes in homeostatic condition and after stimulation.

(Submitter supplied) Transcriptome analysis comparing naive and Listeria monocytogenes-induced spleen memory CD8 T lymphocytes were conducted to identify key functions associated with memory CD8-mediated immune protection. Gene expression analysis was performed on quiescent and re-stimulated CD8 T cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL22408
22 Samples
Download data: CEL
Series
Accession:
GSE86601
ID:
200086601
10.

Gene profiling of naive, virus-induced and inflammatory-induced memory CD8 T lymphocytes in homeostatic condition and after stimulation.

(Submitter supplied) Transcriptome analysis comparing naive, protective and non-protective spleen memory CD8 T lymphocytes were conducted to identify key functions associated with memory CD8-mediated immune protection. Memory CD8 T cells generated in response to influenza or vaccinia infection (Flu-memory and VV-memory) were compared to inflammatory memory cells (TIM) that were generated by peptide in inflammatory context. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL20681
40 Samples
Download data: CEL
Series
Accession:
GSE70763
ID:
200070763
11.

Single cell RNA sequencing of naive and memory B cells

(Submitter supplied) The goal of this study is to compare the transcriptomes of memory and naïve B cells, and provide a resource for single cell analysis of murine B cells during influenza infection.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21626
4 Samples
Download data: FASTA, MTX, TSV
Series
Accession:
GSE181009
ID:
200181009
12.

Control of nutrient uptake by IRF4 orchestrates innate immune memory

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
6 Samples
Download data: CSV, H5AD
Series
Accession:
GSE236556
ID:
200236556
13.

Control of nutrient uptake by IRF4 orchestrates innate immune memory - scRNA-seq

(Submitter supplied) Natural Killer (NK) cells are innate cytotoxic lymphocytes with adaptive immune features, including antigen-specificity, clonal expansion, and memory. As such, NK cells share many transcriptional and epigenetic programs with their adaptive CD8+ T cell siblings. Various signals ranging from antigen, co-stimulation, and proinflammatory cytokines are required for optimal NK cell responses in mice and humans during virus infection; however, the integration of these signals remains unclear. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
2 Samples
Download data: CSV, H5AD
Series
Accession:
GSE236555
ID:
200236555
14.

Control of nutrient uptake by IRF4 orchestrates innate immune memory - ChIP-seq

(Submitter supplied) Natural Killer (NK) cells are innate cytotoxic lymphocytes with adaptive immune features, including antigen-specificity, clonal expansion, and memory. As such, NK cells share many transcriptional and epigenetic programs with their adaptive CD8+ T cell siblings. Various signals ranging from antigen, co-stimulation, and proinflammatory cytokines are required for optimal NK cell responses in mice and humans during virus infection; however, the integration of these signals remains unclear. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: BED
Series
Accession:
GSE235064
ID:
200235064
15.

IFNAR1 Signaling in NK Cells Promotes Persistent Virus Infection

(Submitter supplied) Inhibition of IFN-I signaling promotes the control of persistent virus infection, but the underlying mechanisms remain poorly understood. Here we report that genetic ablation of IFNAR1 specifically in NK cells led to elevated numbers of T follicular helper cells, germinal center B cells, and plasma cells, resulting in hastened virus clearance comparable to IFNAR1 blockade by an IFNAR1 neutralizing antibody. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
8 Samples
Download data: CSV
Series
Accession:
GSE147330
ID:
200147330
16.

SARS-CoV-2 viral persistence in lung alveolar macrophages is controlled by IFN-g and NK cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca fascicularis
Type:
Expression profiling by array
Platform:
GPL29936
65 Samples
Download data: RCC
Series
Accession:
GSE243734
ID:
200243734
17.

SARS-CoV-2 viral persistence in lung alveolar macrophages is controlled by IFN-g and NK cells [BALF_BloodNK_SARSWu_NHP]

(Submitter supplied) SARS-CoV-2 RNA generally becomes undetectable in upper airways after a few days or weeks post-infection. It is unclear however if the virus persists in other parts of the body and which mechanism(s) regulate SARS-CoV-2 persistence. We addressed this question in the macaque model. Replication-competent virus was detected in bronchioalveolar lavages (BAL) macrophages beyond 6 months post-infection. SARS-CoV-2 propagated in BAL macrophages from cell-to-cell. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by array
Platform:
GPL29936
24 Samples
Download data: RCC, TXT
Series
Accession:
GSE243733
ID:
200243733
18.

SARS-CoV-2 viral persistence in lung alveolar macrophages is controlled by IFN-g and NK cells [BALF_NK_SARSWu_NHP]

(Submitter supplied) SARS-CoV-2 RNA generally becomes undetectable in upper airways after a few days or weeks post-infection. It is unclear however if the virus persists in other parts of the body and which mechanism(s) regulate SARS-CoV-2 persistence. We addressed this question in the macaque model. Replication-competent virus was detected in bronchioalveolar lavages (BAL) macrophages beyond 6 months post-infection. SARS-CoV-2 propagated in BAL macrophages from cell-to-cell. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by array
Platform:
GPL29936
20 Samples
Download data: RCC, TXT
Series
Accession:
GSE243732
ID:
200243732
19.

SARS-CoV-2 viral persistence in lung alveolar macrophages is controlled by IFN-g and NK cells [BALF_Macro_SARS_NHP]

(Submitter supplied) SARS-CoV-2 RNA generally becomes undetectable in upper airways after a few days or weeks post-infection. It is unclear however if the virus persists in other parts of the body and which mechanism(s) regulate SARS-CoV-2 persistence. We addressed this question in the macaque model. Replication-competent virus was detected in bronchioalveolar lavages (BAL) macrophages beyond 6 months post-infection. SARS-CoV-2 propagated in BAL macrophages from cell-to-cell. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by array
Platform:
GPL29936
21 Samples
Download data: RCC
Series
Accession:
GSE243731
ID:
200243731
20.

Transcriptional profile of human memory B cells isolated from lung, lung-draining lymph node and PBMCs

(Submitter supplied) RNAseq was performed on human memory B cells isolated from lung, lung-draining lymph nodes and PBMCs to identify differentially expressed genes underpinning tissue localisation.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30209
13 Samples
Download data: CSV, TXT
Series
Accession:
GSE186010
ID:
200186010
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