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Links from GEO DataSets

Items: 18

1.

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
2.
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
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.

Early SIV infection and effects of pathogenic and commensal enteric bacteria on expression in ileum tissue

(Submitter supplied) We used the ileal loop model to assess the effects of enteric bacteria organisms on host gene expression in intestinal tissue independent of and following early SIV infection. SIV infection in the gut causes rapid and severe immune dysfunction and damage to the intestinal structure, this may alter the intimate interaction with lumenal organisms. This study was performed to determine whether early SIV infection, prior to the depletion of CD4+ T cells, can alter interaction of the host with pathogenic Salmonella serovar Typhimurium (ST) or commensal Lactobacillus plantarum (LP), and to further understand the earliest changes to the intestinal mucosa following SIV infection. more...
Organism:
Macaca mulatta
Type:
Expression profiling by array
Platform:
GPL3535
28 Samples
Download data: CEL
Series
Accession:
GSE52589
ID:
200052589
5.

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
6.

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
7.

Host-microbe interactions following L. plantarum administration in SIV-infected and uninfected rhesus macaques

(Submitter supplied) We used microarrays to detail the global gene expression changes in the ileum of SIV-infected and uninfected macaques following administration of L. plantarum.
Organism:
Macaca mulatta
Type:
Expression profiling by array
Platform:
GPL3535
12 Samples
Download data: CEL
Series
Accession:
GSE139271
ID:
200139271
8.

Expression data from rhesus macaque jejunum

(Submitter supplied) The mucosa that lines the gastrointestinal (GI) tracts is an important portal of entry for pathogens and provides the frontline of immune defense against HIV infection. Epithelial barrier dysfunction during HIV infection has largely been attributed to the rapid and severe depletion of CD4 T cells in the gastrointestinal (GI) tract. In this study, the poential role of small non-coding microRNA (miRNA) to contribute to epithelial dysfunction was investigated in the non-human primate SIV model and microarrays were utilized to determine changes in mucosal gene expression (non-miRNA) that could be correlated to miRNA modulatiolns. more...
Organism:
Macaca mulatta
Type:
Expression profiling by array
Platform:
GPL3535
6 Samples
Download data: CEL
Series
Accession:
GSE55359
ID:
200055359
9.

Type I IFN responses in rhesus macaques prevent SIV transmission and slow disease progression

(Submitter supplied) In acute HIV infection immune activation may provide target cells and drive virus replication, which innate immunity may limit. Thus, the net effects of inflammatory mediators, including type I interferon (IFN-I), are unclear. Here, we block IFN-I signaling during pathogenic acute SIV infection with an IFN-I receptor antagonist. Delayed antiviral gene expression, increased SIV reservoir, increased CD4 T cell depletion and accelerated progression to AIDS and death ensue despite decreased T cell activation. more...
Organism:
Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL14954
203 Samples
Download data: TXT
Series
Accession:
GSE53690
ID:
200053690
10.

Cytomegalovirus-mediated expansion of IL-15-responsive innate-memory cells with SIV killing function

(Submitter supplied) We investigated the effects of rhesus CMV (RhCMV) on composition and function of the immune system in young macaques. Within months of infection, RhCMV was associated with impressive changes in antigen presenting cells, T cells, and NK cells—and marked expansion of innate-memory CD8+ T cells. These cells express high levels of NKG2A/C and the IL-2- and IL-15-receptor beta chain, CD122. IL-15 was sufficient to drive differentiation of the cells in vitro and in vivo. more...
Organism:
Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23949
42 Samples
Download data: CSV
Series
Accession:
GSE171978
ID:
200171978
11.

Hallmarks of primate lentiviral immunodeficiency infection recapitulate loss of innate lymphoid cells

(Submitter supplied) Innate lymphoid cells (ILCs) play critical roles in mucosal barrier defense and tissue homeostasis. While ILCs are depleted in HIV-1 infection, this phenomenon is not a generalized feature of all viral infections. Here we show in untreated SIV-infected rhesus macaques (RMs) that ILC3s are lost rapidly in mesenteric lymph nodes (MLN) yet preserved in SIV+ RMs with pharmacologic or natural control of viremia. more...
Organism:
Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19129
11 Samples
Download data: CSV
Series
Accession:
GSE116013
ID:
200116013
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
15.

Gut germinal center regeneration and enhanced anti-viral immunity by mesenchymal stem/stromal (MSC) cells in SIV infection

(Submitter supplied) We performed RNAseq on whole ileum extracts to investigate the underlying gene expression changes associated with MSC administration during chronic SIV infection.
Organism:
Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23949
15 Samples
Download data: TAB
Series
Accession:
GSE171635
ID:
200171635
16.

The Transcriptome of HIV-1 Infected Intestinal CD4+ T cells Exposed to Enteric Bacteria

(Submitter supplied) The gastrointestinal tract is a major site of early HIV-1 replication and death of CD4+ T cells. As HIV-1 replicates in the gut, the protective epithelial barrier gets disrupted, leading to the entry of bacteria into the underlying tissue and the bloodstream, leading to inflammation and clinical complications even in HIV-1-infected patients taking antiviral drugs. Counteracting these pathogenic processes may require in-depth understanding of the molecular pathways that HIV-1 and microbes utilize to infect, functionally alter and/or kill CD4+ T cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
24 Samples
Download data: CEL
Series
Accession:
GSE86404
ID:
200086404
17.

Single cell RNAseq was conducted on mice with TIPE protein knockout to identify the effect of TIPE proteins on immune response [Lung]

(Submitter supplied) Mucosal surfaces are continuously exposed to, and challenged by, numerous commensal and pathogenic organisms. To guard against infections, a majority of the thymus-derived T lymphocytes are deployed at the mucosa. Although chemokines are known to be involved in the mucosal lymphocyte deployment, it is not clear whether lymphocytes enter the mucosa through directed migration or enhanced random migration. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
3 Samples
Download data: CSV, MTX, TSV
Series
Accession:
GSE185256
ID:
200185256
18.

High-dimensional transcriptional analyses of UC Colon comparing RNALater to DMSO collection method

(Submitter supplied) Simultaneous analyses of peripheral and mucosal immune compartments can yield insight into the pathogenesis of mucosal-associated diseases. Although methods to preserve peripheral immune cells are well established, studies involving mucosal immune cells have been hampered by lack of simple storage techniques. We provide a cryopreservation protocol allowing for storage of gastrointestinal (GI) tissue with preservation of viability and functionality of both immune and epithelial cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
72 Samples
Download data: TXT
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