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Series GSE188879 Query DataSets for GSE188879
Status Public on Jan 06, 2023
Title ATAC-seq profiling in CD14+ cells isolated from rhesus macaques vaccinated with V1-deleted DNA/ALVAC/gp120 vaccine [study 2]
Organism Macaca mulatta
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary We analyzed innate and adaptive immune responses elicited by the V1-deleted DNA/ALVAC/gp120/alum vaccine in non-human primates. Following SIVmac251 challenge exposure, we observed reduced risk of SIV acquisition comparing vaccinated animals to controls, confirming th ability of this vaccine strategy in decreasing the risk of SIV acquisition against vaginal exposure. Transcriptome and chromatin accessibility in CD14+ cells were analyzed by RNA-seq and ATAC-seq. Epigenetic reprogramming in CD14+ cells of the cyclic AMP/CREB pathway correlated with vaccine efficacy. The efficacy of V1-delted DNA/ALVAC/gp120/alum vaccine, based on V2-specific antibodies mediating apoptosis of infected cells (V2-ADCC), is complemented by efferocytosis, a cyclic AMP (cAMP)-dependent antiphlogistic engulfment of apoptotic cells by CD14+ monocytes. Our data support the protective role for CREB1 expression in monocytes and posit that efferocytosis, through the prompt and effective removal of apoptotic infected cells, contributes to vaccine efficacy by decreasing inflammation and maintaining tissue homeostasis.
 
Overall design Twelve juvenile (average age 3.91 years, 0.155 SD), female macaques were enrolled in the study. All twelve macaques were immunized twice with V1-deleted DNA-SIV at weeks 0 and 4. At weeks 8 and 12 all macaques were boosted with intramuscular inoculations of 10^8 Plaque Forming Units (PFU) of recombinant ALVAC (vCP2432). At week 12, vaccinated macaques also received 400 μg of v1-delted SIVmac251–M766 protein formulated in alum Alhydrogel. The isolation of CD14+ cells was performed from freshly isolated PBMCs collected at weeks 13. The chromatin accessibility of monocyte population was assessed by Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq).
 
Contributor(s) Bissa M, Kim S, Moles R, Fujiwara S, Hager GL, Franchini G
Citation(s) 36732510
Submission date Nov 15, 2021
Last update date Apr 11, 2023
Contact name Massimiliano Bissa
E-mail(s) massimiliano.bissa@nih.gov
Phone 2407606578
Organization name National Institutes of Health
Department NCI/CCR
Lab AMRVS
Street address 9000 Rockville Pike, bldg 41/ room c303
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platforms (1)
GPL27943 Illumina NovaSeq 6000 (Macaca mulatta)
Samples (24)
GSM5691410 BM228_06BA_V1-deleted-DNA/DNA/ALVAC/ALVAC+gp120_Week 13
GSM5691411 BM232_T63_V1-deleted-DNA/DNA/ALVAC/ALVAC+gp120_Week 13
GSM5691412 BM247_T96_V1-deleted-DNA/DNA/ALVAC/ALVAC+gp120_Week 13
Relations
BioProject PRJNA780552
SRA SRP346215

Download family Format
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Supplementary file Size Download File type/resource
GSE188879_RAW.tar 44.6 Mb (http)(custom) TAR (of NARROWPEAK)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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