📢Travel Grant Opportunity for #ECRs
🙌Proud to announce that #EFIS, together with the @eurjimmunol.bsky.social, is offering 5 travel grants (€1,000 each) to support attendance at the GRC!
💡Grants will be awarded based on scientific merit, career stage + inclusion criteria.
⏰Deadline: 1 May 2026
Posts by Iannacone Lab
With @hiroshi-ichise.bsky.social, closing the @ccii-kyoto.bsky.social workshop on advanced imaging and image analysis in Kyoto.
Thanks to Guolan Lu (Stanford), @iannaconelab.bsky.social, Andrea Radtke (Leica), Yuki Sugiura (CCII), and Johanne T. Jacobsen for great lectures and practicals!
Matteo Iannacone @iannaconelab.bsky.social gave a tour de force presentation on liver immunity, hosted by @hiroshi-ichise.bsky.social as part of the CCII workshop on Advanced Tissue Imaging & Image Analysis
#Immunology #TissueImmunity
www.ccii.med.kyoto-u.ac.jp/en/event/eve...
Review @natrevimmunol.nature.com @gustaveroussy.fr @iannaconelab.bsky.social
Kupffer cells in liver homeostasis and disease: from immune sentinels to metabolic gatekeepers
www.nature.com/articles/s41...
Great fun to write this review on Kupffer cells with Florent Ginhoux and Paul Kubes, covering origin, diversity and roles in immunity and metabolism, now out in @natrevimmunol.nature.com. Huge credit to Bruna Araujo David, Francesco Andreata and Camille Blériot for driving this work. t.co/rGpmTMRddV
This calls for a shift in vaccine design:
• target early, conserved viral proteins
• build tissue-resident immunity
• combine antibodies and T cells
Great collaboration with
Leo Swadling, Valeria Fumagalli and Mala K. Maini
Implications:
• T cells can act at inception, not just during clearance
• Standard readouts (serology/PCR) miss these events
• True exposure and immunity are likely underestimated
→ We need to measure what T cells actually do
What is abortive infection?
Virus enters cells → limited early replication →
🛑 Pre-existing memory T cells eliminate infected cells
Before there is:
• detectable viral load (PCR)
• antibody induction (seroconversion)
• clinical disease
→ infection is stopped “below the radar”
Neutralizing antibodies are not the whole story.
In our Comment in Nature Reviews Immunology, we highlight an alternative mode of protection:
👉 T cells can eliminate infection at its earliest stage — before it becomes detectable
We term this “abortive infection”
🔗 rdcu.be/fbq8p
Thread 1/4
Excited to organize @keystoneSymposia.bsky.social Tissue and Spatial Immunology with @leilaakkari.bsky.social and Hai Qi in February 2027! Join us to explore emerging research in Banff! keysym.us/KSSpatialImmune27 #KSSpatialImmune27
Join us for the 2026 GRC Immunochemistry and Immunobiology "Immune Circuitry and Molecular Pathways in Tissue Homeostasis, Infection, and Disease" in beautiful Barcelona. June 28 - July 3, 2026. Great lineup of speakers! www.grc.org/immunochemis...
Don't miss the 2026 Global Immunotalks!
📢Want to speak at the #CancerImmuno conference?
Good news! The chairs have released additional short talk slots and extended the submission deadline to 26 February 2026!
Submit your abstract for a chance to present your work alongside leading researchers in the field.
👉 Register now: bit.ly/3NRB7Iu
📩 Submit the paper link + short statement (≤250 words) to ejied@wiley.com by 15 April 2026.
The winner will be selected by EJI editors together with @yefis-immunology.bsky.social representatives.
#Immunology #ImmunoSky #AcademicSky #EarlyCareerResearchers #ECR
@efis-immunology.bsky.social
🏆Nominations are OPEN for the 2026 EJI-EFIS Prize for the ECR Article of the Year!
Best paper published in EJI (2025) by an early-career researcher wins €5,000 + travel grant to ECI 2027 (Florence)✈️
🔗 Details & eligibility: bit.ly/41GeiMi
🫵 Self-nominations encouraged!
Great story from the Nieswandt lab in Science: uncovering a non-classical platelet mechanism that drives inflammation via integrin- and tetraspanin-rich tethers. A fresh angle on thrombo-inflammation. Happy to be part of this work!
www.science.org/doi/10.1126/...
Thanks to Chiara Perucchini and Chiara Vespari for their critical contribution
9/ Read the paper here 👉 onlinelibrary.wiley.com/doi/10.1002/...
And stay tuned — exciting new discoveries on liver Tregs are coming soon 👀🧬
7/ Bottom line: this work reframes ARTC2 blockade from a default reagent to a rational, cost-effective experimental choice.
8/ Proud of the team — led by Caitlin Abbott, with Violette Mouro and colleagues — for turning a technical challenge into actionable guidance for the field.
6/ Practical takeaway 💡
• Studying activated/eTregs at steady state? ARTC2 blockade may be optional.
• Profiling CD44^mid Tregs or working in inflammatory settings? ARTC2 blockade is essential.
5/ Key insight: hepatic Treg subsets are not equally sensitive to ARTC2–P2RX7 activation.
Less-activated, tissue-resident Tregs are preferentially lost or skewed without protection.
4/ During liver inflammation, ARTC2 blockade becomes critical: it boosts overall Treg yield and prevents phenotypic distortion — again with the strongest effect on CD44^mid Tregs.
3/ At steady state, ARTC2 blockade has a selective benefit: it markedly improves recovery and preserves phenotype of CD44^mid (less-activated) Tregs, while having minimal impact on effector-like eTregs.
1/ New from our lab 🧪
ARTC2 blockade is widely used to protect tissue Tregs — but when is it truly essential, and for which subsets?
2/ In this @eurjimmunol.bsky.social update, we dissect the subset-specific and context-dependent effects of ARTC2 blockade on hepatic Treg recovery.
Thrilled to contribute to this landmark consensus effort led by Dave Masopust and Rafi Ahmed. A major step toward clearer, shared T cell nomenclature for the field. www.nature.com/articles/s41...
Honoured to see our @natimmunol.nature.com study highlighted in a thoughtful @jhepatology.bsky.social commentary on the IL-27/Kupffer cell axis in chronic HBV — a great summary of why tissue immunity matters and of our work.
Paper: tinyurl.com/yt652mxa
Commentary: tinyurl.com/56pke5x5
New review out! 😊 20 years after it’s discovery, with @iannaconelab.bsky.social we decided to bring together what we currently know about this cytokine and how it shapes CD8 T cell responses. A small contribution to make sense of a field that is moving fast 🌈 @cp-trendsimmuno.bsky.social
New review out in @cp-trendsimmuno.bsky.social! With @valentinavenzin.bsky.social, we revisit IL-27 as a central regulator of CD8⁺ T cell fate — integrating insights from infection, cancer, and autoimmunity, and outlining its therapeutic potential. www.sciencedirect.com/science/arti...
#CancerImmuno speaker list is live!📢
Join us in sunny Lisbon, July 2026. Register now and submit your talk to share your research.
Early Bird Deadline: 15 Jan 2026
👉 Click here to register: bit.ly/4qZVqmd
#FusionImmunology #FusionCancerResearch
🎤 Our next episode it out!
We chat with Professor Matteo Iannacone ( @iannaconelab.bsky.social ) from @@unisr.bsky.socialabout his work understanding the generation of dysfunctional adaptive immune cells in chronic #HepatitisBVirus infection.
🎧 Listen now: https://bit.ly/4o2W8xa