Jennifer Juno
@jenjuno.viralvaxlab.com
1K followers 320 following 23 posts
🇨🇦 in 🇦🇺 Scientist. Geek. Feminist. She/her. Lab head (viralvaxlab.com) at the Doherty Institute and University of Melbourne, interested in all things CD4/TFH/vaccine and virus-related. I stare at dots a lot.
Posts Media Videos Starter Packs
Reposted by Jennifer Juno
angierasmussen.bsky.social
I am always so impressed by @marioskoutsakos.viralvaxlab.com’s elegant work on influenza B virus vaccines. Congratulations, Marios, on your Early Career Researcher Award! #19vaccinecongress
Reposted by Jennifer Juno
msmacrophage.bsky.social
Publication alert: "No evidence of immune exhaustion after repeated SARS-CoV-2 vaccination in vulnerable and healthy populations" ‪@natcomms.nature.com‬ The backstory is particularly interesting-it's a tale of the conflicting needs of scientists & decision makers in times of disinformation ....1/n
No evidence of immune exhaustion after repeated SARS-CoV-2 vaccination in vulnerable and healthy populations
Nature Communications - Repeated vaccination is needed to maintain high levels of SARS-CoV-2 immunity in vulnerable populations, but there is concern that it could lead to immune exhaustion. Here,...
rdcu.be
Reposted by Jennifer Juno
groomlab.bsky.social
Excited to have our latest research published in @jem.org this week and also highlighted by @natrevimmunol.nature.com
@wehi-research.bsky.social @benjbroom.bsky.social
jenjuno.viralvaxlab.com
Fantastic work from @labphan.bsky.social and @mlmunier.bsky.social combining mouse models and clinical studies to understand B cell recall following booster vaccination. Check out the paper and thread below! ⤵️
jenjuno.viralvaxlab.com
Happy to report that Mitchell's paper on CD4 T cells and AIM assays is now available online at Science Advances!

www.science.org/doi/10.1126/...

Thanks to all our collaborators in @viralvaxlab.bsky.social and @thedohertyinst.bsky.social, including @assocprofashhaque.bsky.social lab
jenjuno.viralvaxlab.com
Great new story exploring how B cells can recognise glycans (and still get T cell help!) from @precisionvaxlab.bsky.social and team!
precisionvaxlab.bsky.social
New preprint alert 🚨

My team and I are pleased to share our most recent story about how bacterial pathogen (Streptococcus pyogenes, Strep A) exposure induces antibody responses against glycan and protein antigens.

For paper: SSRN ssrn.com/abstract=519...
biorxiv : doi: doi.org/10.1101/2025...
jenjuno.viralvaxlab.com
What do you need them for, Julie? We might have other lines that would work for your experiments.
Reposted by Jennifer Juno
insight.jci.org
Should you get the COVID mRNA and flu vaccines in the same or opposite arms?

Randomised trial by Lee, Selva, et al. suggests it is preferable to administer the vaccines at different sites. buff.ly/3D4gX95
jenjuno.viralvaxlab.com
Unfortunately, Melbourne isn't going to be quite as seamless of an experience...
Reposted by Jennifer Juno
labliston.bsky.social
If any American immunologists want to write an op-ed for @immunolcellbiol.bsky.social on the impact of the new executive orders, please contact me
jenjuno.viralvaxlab.com
9/9 Thanks to all our collaborators who helped out with the study, and congrats to Mitchell, who persevered through a lot of possible activation marker combinations!
jenjuno.viralvaxlab.com
8/9 In short, we suggest in vitro stimulation activates ag-specific T cells, which secrete cytokines and activate Treg and Th17/22 cells. Without careful phenotyping, all of these cells can get picked up as AIM+, accounting for the Th17-like memory cells found in many virus-specific AIM datasets.
jenjuno.viralvaxlab.com
7/9 Mitch sorted tetramer-specific cells, labelled them, and added them back into PBMC before stimulating with the relevant peptide.

He was able to show that ag-specific CD4 cells downregulate CXCR4 while upregulating 4-1BB/CD137, giving us a more accurate way to define antigen specificity.
jenjuno.viralvaxlab.com
6/9 Unfortunately, these cytokine-activated cells upregulated almost all of the AIM markers we normally use.

One difference, however, appeared to be CXCR4. TCR-mediated activation efficiently downregulates CXCR4 expression, while cytokine-mediated activation has much less of an impact.
jenjuno.viralvaxlab.com
5/9 Using RNAseq and confirmatory FACS, Mitch showed that CD39+ Tregs and Th17/Th22 cells expressing CCR6 and high levels of CD26 were being activated through the transwell via a mechanism involving IL-2.

These same subsets are also found during standard peptide-based AIM assays.
jenjuno.viralvaxlab.com
4/9 Possibly!

In a transwell assay, anti-CD3/CD28 stimulation can drive T cells in an adjacent chamber to express common activation markers (CD25, OX-40, 4-1BB, CD40L).

All of these responding cells had a memory phenotype, and were strongly enriched for CCR6 expression.
jenjuno.viralvaxlab.com
3/9 Mitch ruled out a few options: CD4 cells don’t upregulate CCR6 during peptide stimulation, and the AIM+ CCR6+ cells don’t usually contain clonally expanded TCRs.

Does that mean that AIM assays might be picking up cases of TCR-independent activation?
jenjuno.viralvaxlab.com
2/9 Recently, though, we’ve been bothered by something we couldn’t explain: we find a lot of Th17-like, CCR6+ SARS-CoV-2 spike-specific CD4 T cells in our AIM assays, but we never see these cells when we use spike-specific class II tetramers.

Why?