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Links from GEO DataSets

Items: 14

1.

Deep transcriptional sequencing of mucosal challenge compartment from rhesus macaques acutely infected with simian immunodeficiency virus implicates loss of cell adhesion preceding immune activation

(Submitter supplied) Recent studies of nonhuman primates (NHPs) have suggested that during the acute phase of infection, antiviral mucosal immunity is restricting viral replication in the primary infection compartment. These studies imply that HIV achieves systemic infection as a consequence of a failure in host antiviral immunity. Here, we used high-dose intrarectal inoculation of rhesus macaques with SIVmac251 to examine how the mucosal immune system is overcome by SIV during acute infection. more...
Organism:
Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13766
23 Samples
Download data: TXT
Series
Accession:
GSE56845
ID:
200056845
2.

miRNA expression changes in small intestinal lamina propria leukocyte samples during the course of SIV infection of rhesus macaques

(Submitter supplied) This study describes differential miRNA expression in small intestinal lamina propria leukocyte samples longitudinally during the course of SIV infection of rhesus macaques. Notably, the T-cell activation associated miR-15b, miR-142-3p, miR-142-5p and miR-150 expression was significantly downregulated at 90 and 180DPI. Further, reporter and overexpression assays validated IRAK1 as a direct miR-150 target. more...
Organism:
Homo sapiens; Macaca mulatta
Type:
Expression profiling by RT-PCR
Platform:
GPL17797
25 Samples
Download data: TXT
Series
Accession:
GSE77134
ID:
200077134
3.

Reduced chronic lymphocyte activation following Interferon-α blockade in the acute phase of SIV infection in rhesus macaques

(Submitter supplied) Pathogenic HIV/SIV infection of humans and rhesus macaques (RMs) induces persistently high production of type-I interferon (IFN-I) which is thought to contribute to disease progression. To elucidate the specific role of IFN in SIV pathogenesis, 12 RMs were treated prior to i.v. SIVmac239 infection with a high or a low dose of an antibody (AGS-009) that neutralizes most IFN subtypes, and compared with six mock-infused, SIV-infected controls. more...
Organism:
Macaca mulatta; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
107 Samples
Download data: TXT
Series
Accession:
GSE110617
ID:
200110617
4.

Expression data from rhesus macaque colon, jejunum, and lung

(Submitter supplied) The mucosa that lines the respiratory and gastrointestinal (GI) tracts is an important portal of entry for pathogens and provides the frontline of immune defense against HIV infection. Using the simian immunodeficiency virus (SIV) rhesus macaque model, we have performed a comparative analysis of host gene expression in the lung and GI mucosa in response to SIV infection and antiretroviral therapy. Microarrays were used to characterize changes in gene expression in the colonic, jejunal, and pulmonary (lung) mucosa that occur during chronic SIV infection in the presence or absence of antiretroviral therapy.
Organism:
Macaca mulatta
Type:
Expression profiling by array
Dataset:
GDS4993
Platform:
GPL3535
32 Samples
Download data: CEL
Series
Accession:
GSE51615
ID:
200051615
5.
Full record GDS4993

Chronic simian immunodeficiency virus infection: colon, jejunum and lung

Analysis of colon, jejunum and lung from therapy-naïve, SIV-infected males. Gut and lung mucosa are important entry portals for pathogens and provide innate immune defense against infection. Results provide insight into molecular mechanisms underlying mucosal immune response during SIV infection.
Organism:
Macaca mulatta
Type:
Expression profiling by array, count, 2 infection, 3 tissue sets
Platform:
GPL3535
Series:
GSE51615
23 Samples
Download data: CEL
6.

Cannabinoid attenuation of intestinal inflammation in chronic SIV-infected rhesus macaques involves differential modulation of pro-inflammatory microRNA/gene expression and T-cell activation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca mulatta; Homo sapiens
Type:
Expression profiling by array; Expression profiling by RT-PCR
Platforms:
GPL17837 GPL16027
39 Samples
Download data: TXT
Series
Accession:
GSE121441
ID:
200121441
7.

MicroRNA profiling of colon tissue samples following chronic Delta-9-Tetrahydrocannabinol (THC) treatment to chronically SIV-infected rhesus macaques

(Submitter supplied) The study describes miRNA expression in colon tissue following delta 9 tetrahydrocannabinol (Δ9-THC) administration to chronically SIV-infected rhesus macaques. To identify the underlying molecular mechanisms underlying its anti-inflammatory effects, we simultaneously profiled miRNA and mRNA expression in colon of chronically simian immunodeficiency virus (SIV)-infected rhesus macaques (RMs) administered either vehicle (VEH/SIV; n=9) or Δ9- tetrahydrocannabinol (THC; THC/SIV; n=8). more...
Organism:
Homo sapiens; Macaca mulatta
Type:
Expression profiling by RT-PCR
Platform:
GPL17837
23 Samples
Download data: XLSX
Series
Accession:
GSE121440
ID:
200121440
8.

Cannabinoid attenuation of intestinal inflammation in chronic simian immunodeficiency virus (SIV)-infected rhesus macaques involves differential modulation of pro-inflammatory microRNA/gene expression and T-cell activation

(Submitter supplied) We profiled and characterized mRNA expression in colon of 12 chronically SIV-infected rhesus macaques (RMs) receiving vehicle (n=7) or delta-9-tetrahydrocannabinol (THC) and 4 uninfected control macaques. Further analysis identified significant downregulation of genes associated with ion transport, epithelial barrier integrity/function, protection against oxidative injury, double stranded DNA damage repair and autophagy. more...
Organism:
Macaca mulatta
Type:
Expression profiling by array
Platform:
GPL16027
16 Samples
Download data: TXT
Series
Accession:
GSE121439
ID:
200121439
9.

miRNA profiling of Macaca mulatta intact colon samples during acute SIV infection

(Submitter supplied) This study describes differential miRNA expression in intact colon tissue during acute SIV infection of rhesus macaques. Nine miRNAs were found to be significantly affected by infection, with 5 down-regulated and 4 up-regulated miRNAs. The expression of one upregulated miRNA was further characterized and found to be significantly elevated specifically in response to SIV replication and not immune activation/inflammation accompanying SIV infection.
Organism:
Macaca mulatta; Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL17797
15 Samples
Download data: TXT
Series
Accession:
GSE56624
ID:
200056624
10.

Plasma Cell Niche

(Submitter supplied) Sorted cells from bone marrow and rectal mucosa of SIV-infected rhesus macaques were analyzed for expression of factors associated with plasma cell recruitment, adhesion, or maintenance mRNA expression anaylsis was performed on 16 CD2-CD19-CD20-HLA-DR+ and 16 CD2-CD19-CD20-HLA-DR- bone marrow cells, and 7 CD2-CD19-CD20-HLA-DR+ and 3 CD2-CD19-CD20-HLA-DR- rectal cells using a custom CodeSet produced by NanoString Technologies containing 44 niche factor genes of interst, 12 cell-type specific genes, and 9 reference genes identified in Genevestigator.
Organism:
Macaca mulatta
Type:
Expression profiling by array
Platform:
GPL21884
42 Samples
Download data: RCC
Series
Accession:
GSE81609
ID:
200081609
11.

miRNA profiling of Macaca mulatta intact duodenum samples following chronic Delta9 Tetrahydrocannabinol (Δ9-THC) treatment to SIV infected rhesus macaques

(Submitter supplied) The study describes miRNA expression in intact duodenum following chronic delta 9 tetrahydrocannabinol (Δ9-THC) administration to SIV-infected rhesus macaques. Chronic Δ9-THC administration to uninfected macaques significantly and positively modulated intestinal miRNA expression by increasing the total number of differentially expressed miRNAs from 14 to 60 days post infection (DPI). At 60DPI, ~28% of miRNAs showed decreased expression in VEH/SIV compared to none in the THC/SIV group. more...
Organism:
Macaca mulatta; Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL17837
44 Samples
Download data: XLS
Series
Accession:
GSE61654
ID:
200061654
12.

Wound healing mechanisms in pathogenesis control in natural SIV host species

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca mulatta; Chlorocebus aethiops
Type:
Expression profiling by high throughput sequencing
4 related Platforms
124 Samples
Download data
Series
Accession:
GSE111234
ID:
200111234
13.

Wound healing mechanisms in pathogenesis control in natural SIV host species [monocytes]

(Submitter supplied) We devised a systems biology approach to investigate the early host response to high-dose rectal SIV transmission, by transcriptomic comparative analysis of a natural reservoir host SIV model species, African green monkeys (AGMs – Chlorocebus sabaeus, N=28) and a pathogenic model, rhesus macaques (RMs - Macaca mulatta, N=24).on rectal tissues for both AGMs and RMs.
Organism:
Chlorocebus aethiops; Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21120 GPL22096
45 Samples
Download data: TXT
Series
Accession:
GSE111233
ID:
200111233
14.

Wound healing mechanisms in pathogenesis control in natural SIV host species [rectal tissue]

(Submitter supplied) We devised a systems biology approach to investigate the early host response to high-dose rectal SIV transmission, by transcriptomic comparative analysis of a natural reservoir host SIV model species, African green monkeys (AGMs – Chlorocebus sabaeus, N=28) and a pathogenic model, rhesus macaques (RMs - Macaca mulatta, N=24).on rectal tissues for both AGMs and RMs.
Organism:
Chlorocebus aethiops; Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24584 GPL14954
79 Samples
Download data: TXT
Series
Accession:
GSE111077
ID:
200111077
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Supplemental Content

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