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Series GSE253538 Query DataSets for GSE253538
Status Public on Mar 29, 2024
Title Cynomolgus macaques as a translational model of human immune responses to yellow fever 17D vaccination
Organism Macaca fascicularis
Experiment type Expression profiling by high throughput sequencing
Summary The non-human primate (NHP) model (specifically rhesus and cynomolgus macaques) has facilitated our understanding of the pathogenic mechanisms of yellow fever (YF) disease and allowed evaluation of safety and efficacy of YF-17D vaccines. However, the accuracy of this model in mimicking vaccine-induced immunity in humans remains to be fully determined. We used a system biology approach to compare hematological, biochemical, transcriptomic, innate and antibody-mediated immune responses in cynomolgus macaques and human participants following YF-17D vaccination. Immune response progression in cynomolgus macaques followed a similar course as in adult humans, but with slightly earlier onset. Yellow fever virus neutralizing antibody responses occurred earlier in cynomolgus macaques (by Day 7 [D7]), but titers >10 were reached in both species by D14 post-vaccination and were not significantly different by D28 (PRNT50 titers 3.6 Log vs 3.5 Log in cynomolgus macaques and human participants, respectively; p = 0.821). Changes in neutrophils, NK cells, monocytes, T and B cell frequency were higher in cynomolgus macaques and persisted for four weeks versus less than two weeks in humans. Low levels of systemic inflammatory cytokines (IL-1Ra, IL-8, MIP-1α, IP-10, MCP-1 or VEGF) were detected in either or both species, but with no or only slight changes versus baseline. Similar changes in gene expression profiles were elicited in both species. These included enriched and up-regulated type I IFN-associated viral sensing, antiviral innate response, and dendritic cell activation pathways D3–D7 post-vaccination in both species. Hematological and blood biochemical parameters remained relatively unchanged versus baseline in both species. Low level YF-17D viremia (RNAemia) was transiently detected in some cynomolgus macaques (28% [5/18]) but generally absent in humans (except one participant [5%; 1/20]). Importance: Cynomolgus macaques were confirmed as a valid surrogate model for replicating YF-17D vaccine-induced responses in humans, and suggest a key role for type I IFN.
 
Overall design Whole blood from 12 male cynomolgus macaques (Macaca fascicularis; Noveprim, Mauritius) aged 2.7 to 5.4 years was collected before vaccination at D –21, and after vaccination at D1, D3, D7, D14 and D28.
 
Contributor(s) Chautard E, Mantel N, Piras F, Courtois V, Raynal F
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Submission date Jan 18, 2024
Last update date Mar 29, 2024
Contact name Emilie Chautard
E-mail(s) emilie.chautard@sanofi.com
Organization name Sanofi
Street address 1541 Avenue Marcel Mérieux
City Marcy L'Etoile
ZIP/Postal code 69280
Country France
 
Platforms (1)
GPL22523 Illumina NextSeq 500 (Macaca fascicularis)
Samples (81)
GSM8022718 CCA034, YF-17D vaccination, day 1, rep 1
GSM8022719 CCA034, YF-17D vaccination, day -21, rep 1
GSM8022720 CCA034, YF-17D vaccination, day 3, rep 1
Relations
BioProject PRJNA1066246

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE253538_Count_Annotation.txt.gz 1.1 Mb (ftp)(http) TXT
GSE253538_raw_counts.txt.gz 2.5 Mb (ftp)(http) TXT
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Raw data are available in SRA

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