YF17D vaccination rapidly induces master transcription factors upstream of genes involved in multiple arms of the immune response
Gaucher et al. used gene expression arrays (Illumina BeadChips V2) to study gene expression profiles in whole blood 3, 7, 10, 14, and 60 days post YF17D vaccination in 40 healthy individuals. They found significant changes in the expression of 594 genes, which peaked on days 3 and 7 post vaccination. To identify the transcription factors upstream of these genes, independent component analysis followed by gene set enrichment was performed. Interestingly, three major nodes of transcriptional regulation of downstream target genes were identified as early as day 3 post vaccination: interferon regulatory factor (IRF)7, signal transducer and activator of transcription (STAT)1 and v-ets erythroblastosis virus E26 oncogene homolog 2 (avian) (ETS2). Functionally, these transcriptional nodes and many of the identified genes were associated with Toll-like receptor (TLR), interferon-γ induction, complement factors, macrophage/dendritic cell (DC), natural killer (NK)- and B-cell activation. Results were validated by quantitative real-time PCR in a subset of 7 donors.
Upfront stimulation of the innate immune arm: YF17D vaccination activates components of the inflammasome complex upregulating IL-1β production shortly after inoculation
The inflammasome is a cytoplasmic multiprotein complex that activates caspase-1 and - 5, leading to the processing and secretion of the pro-inflammatory cytokines, interleukin(IL)-1β, IL-18, and IL-33 [
18]. Inflammasomes interact with TLR to mediate appropriate responses to pathogenic triggers constituting a substantial part of the innate immune response. Gaucher
et al. showed that caspase-1 and −5 were upregulated at the RNA level as early as 3 days after YF17D vaccination. Moreover, other genes involved in the production of IL-1β, namely IL-1R1 and -1RN, were also modulated by the vaccine. To functionally validate these findings, they incubated DCs with live and UV-inactivated YF17D vaccine and showed a marked increase in IL-1β production confirming that YF17D vaccine activates components of the inflammasome complex, and that viral replication was not required for this activation.
YF17D vaccination induces proliferation and expansion of various leukocyte subsets
Does the up-regulation of genes associated with activation of various leukocyte subsets result in their proliferation? To answer this question, peripheral blood mononuclear cells (PBMCs) from a number of individuals were stained pre- and post vaccination for the proliferation marker Ki67 in addition to lineage and activation specific markers. The frequencies of both the CD4- and CD8-positive lymphocyte subsets increased, along with NK cells, monocytes and B cells. Cell proliferation peaked within 7 to 14 days post vaccination and then declined to baseline. These results confirmed the widespread mobilization of all major cellular subsets early after YF17D vaccination.
A durable activation of the adaptive immune arm: YF17D vaccination induces an early YF-specific mixed Th1/Th2 response that appears early and is persistent
To further define which part of the adaptive immune arm is activated by the vaccine, PBMCs, obtained day 28 or day 60 post vaccination, were activated with YF17D-derived peptide pools. The pattern of cytokine secretion was determined using cytometric bead assays (CBA) and intracellular cytokine staining. Although the cytokine patterns varied substantially among individuals, most had mixed Th1/Th2 responses with high levels of TNF; CD4+ T cells produced IL-2 or IFN-γ, confirming the Th1 component of the immune response. In addition, YF-specific central memory responses could be detected in PBMCs one year post vaccination. Thus, the vaccine not only induced a strong innate immune response early after vaccination, but also brisk and persistent Th1/Th2 adaptive responses.
Recapitulation of the central immune response to YF17D vaccination in vitro
The authors then took advantage of the MIMIC system, which simulates the human immune response in a high-throughput method enabling rapid, clinically relevant predictions about the efficacy of vaccines. This system uses pheresis-derived PBMCs and purified leukocyte sub-populations (monocytes, T cells, and B cells) from healthy donors to simulate vaccination site and lymphoid tissue interactions between cells in response to stimulation with a vaccine of interest. Using this system, Gaucher et al. validated the multi-lineage response to YF17D vaccination (and UV-inactivated vaccine) including Th1/Th2 responses. Moreover, gene expression analysis identified the same central nodes of transcription as those described after vaccination with YF17D in healthy individuals.
Discussion, expert commentary and five-year view
How can we best assess the potency of vaccines? For the systematic development of a successful vaccination strategy, it is mandatory to develop ‘read out systems’ or ‘correlates of immune-mediated protection’ (COP) that would reliably predict immune responses to novel vaccines
in vivo [
19]. Fortunately, there is an expanding knowledge on the molecular mechanisms of immune responses and on the immunological parameters that correlate best with lasting protection [
8]. As expected, this has not been a simple task and COPs have continued to lag behind the development of novel vaccines [
4,
5,
7,
8,
14,
19,
20]. This is exemplified by the development of vaccines for Rotavirus: prompted by the emergence of severe deadly disease, intense work on vaccine development for this virus started in the early 1980’s and since 2006 two vaccines have been licensed in many countries. Nevertheless, to date, in spite of the intense work in this area, COPs for these two vaccines are still not well defined [
21].
Gaucher et al. have used functional genomics and flow cytometric analysis to determine the immune response to the very effective YF17D vaccine. YF17D vaccination resulted in a rapid and transient modulation of a large number of genes linked to activation of several components of the immune system spanning the innate and adaptive arms. Multiple unique interactions between the various effector arms of the immune system were observed, which are most likely responsible for the long-term protective immunity induced by the vaccine. However, it remains elusive which of these events post YF17D vaccination are essential and which ones are dispensable. This might become evident in the future when other vaccines are evaluated using the same approach. Nevertheless, we expect that some of the findings of this study will be either integrated into existing COPs or will facilitate the development of new COPs.
While genomics has been successfully used to identify new vaccine antigens [
22], Gaucher’s
et al. study highlights that genomics is also a promising tool for evaluating vaccine induced immune responses. Is it possible in the future to develop and test vaccines using solely genomics? Most likely not, however genomics will help us to better understand vaccine induced immune responses and might prevent failures like the STEP HIV vaccine trial. Another noteworthy result of the study is that the results of the human vaccine study correlated well with the results obtained using the
in vitro MIMIC system. If confirmed in future studies, the MIMIC system might thus represent an efficient screening system to evaluate vaccines before conducting costly phase I clinical studies in humans.
In summary, Gaucher
et al. used functional genomics to attempt to answer a question that has occupied a central place in the field of vaccine research since its beginning: How can we best evaluate the potency of a vaccine? Their results are encouraging and should entice the field to develop novel vaccine evaluation strategies. To close with Churchill, Gaucher’s
et al. study ‘is not the end. It is not even the beginning of the end. But it is, perhaps, the end of the beginning [
23].’
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