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Series GSE188586 Query DataSets for GSE188586
Status Public on Dec 23, 2021
Title CD4+CCR6+ T cells dominate the BCG-induced transcriptional signature
Organism Homo sapiens
Experiment type Methylation profiling by array
Summary The century-old Mycobacterium bovis Bacillus Calmette-Guerin (BCG) remains the only licensed vaccine against tuberculosis (TB). Despite this, there is still a lot to learn about the immune response induced by BCG, both in terms of phenotype and specificity. Here, we investigated immune responses in adult individuals pre and 8 months post BCG vaccination. We specifically determined changes in gene expression, cell subset composition, DNA methylome, and the TCR repertoire induced in PBMCs and CD4 memory T cells associated with antigen stimulation by either BCG or a Mycobacterium tuberculosis (Mtb)-derived peptide pool. Following BCG vaccination, we observed increased frequencies of CCR6+ CD4 T cells, which includes both Th1* and Th17 subsets, and mucosal associated invariant T cells (MAITs). A large number of immune response genes and pathways were upregulated post BCG vaccination with similar patterns observed in both PBMCs and memory CD4 T cells, thus suggesting a substantial role for CD4 T cells in the cellular response to BCG. These upregulated genes and associated pathways were also reflected in the DNA methylome. We described both qualitative and quantitative changes in the BCG-specific TCR repertoire post vaccination, and importantly found evidence for similar TCR repertoires across different subjects. The immune signatures defined herein can be used to track and further characterize immune responses induced by BCG, and can serve as reference for benchmarking novel vaccination strategies.
 
Overall design 8 sample DNAs were isolated from the PBMC cells using AllPrep DNA/RNA Mini Kit (Qiagen, Germany). DNA concentration was measured by Qubit fluorometer. DNA samples were bisulphite converted, amplified, fragmented and hybridized to an Illumina Infinium Human Methylation EPIC Bead Chip and scanned.
 
Contributor(s) Singhania A, Dubelko P, Chronister WD, Muskat K, Das J, Phillips EJ, Mallal SA, Seumois G, Vijayanand P, Sette A, Lerm M, Peters B, Arlehamn CL
Citation(s) 34902786
Submission date Nov 10, 2021
Last update date Dec 24, 2021
Contact name Jyotirmoy Das
E-mail(s) [email protected]
Organization name Linköping University
Department Department of Biomedical and Clinical Sciences
Lab Lab 1, Floor 12
Street address Sandbäcksgatan
City Linköping
ZIP/Postal code 58183
Country Sweden
 
Platforms (1)
GPL21145 Infinium MethylationEPIC
Samples (8)
GSM5686090 C1-before
GSM5686091 C2-after
GSM5686092 C3-before
Relations
BioProject PRJNA779456

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE188586_RAW.tar 161.2 Mb (http)(custom) TAR
GSE188586_signal_intensities.txt.gz 36.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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