𝗔𝘅𝗼𝗹𝗼𝘁𝗹𝘀 𝗿𝗲𝗴𝗿𝗼𝘄 𝗮 𝘁𝗵𝘆𝗺𝘂𝘀 𝗳𝗿𝗼𝗺 𝘀𝗰𝗿𝗮𝘁𝗰𝗵


🧠 𝗔 𝗽𝗮𝗽𝗲𝗿 𝗮 𝗱𝗮𝘆 𝗸𝗲𝗲𝗽𝘀 𝗯𝗿𝗮𝗶𝗻 𝗱𝗲𝗰𝗮𝘆 𝗮𝘄𝗮𝘆 🧠
Tuesday 30 December 2025

𝘛𝘩𝘪𝘴 𝘴𝘵𝘶𝘥𝘺 𝘴𝘩𝘰𝘸𝘴 𝘵𝘩𝘢𝘵 𝘢𝘹𝘰𝘭𝘰𝘵𝘭𝘴 𝘤𝘢𝘯 𝘧𝘶𝘭𝘭𝘺 𝘳𝘦𝘨𝘦𝘯𝘦𝘳𝘢𝘵𝘦 𝘢 𝘧𝘶𝘯𝘤𝘵𝘪𝘰𝘯𝘢𝘭 𝘵𝘩𝘺𝘮𝘶𝘴 𝘢𝘧𝘵𝘦𝘳 𝘤𝘰𝘮𝘱𝘭𝘦𝘵𝘦 𝘳𝘦𝘮𝘰𝘷𝘢𝘭, 𝘳𝘦𝘷𝘦𝘢𝘭𝘪𝘯𝘨 𝘢 𝘮𝘪𝘥𝘬𝘪𝘯𝘦-𝘥𝘳𝘪𝘷𝘦𝘯 𝘱𝘳𝘰𝘨𝘳𝘢𝘮 𝘵𝘩𝘢𝘵 𝘳𝘦𝘣𝘶𝘪𝘭𝘥𝘴 𝘵𝘩𝘺𝘮𝘪𝘤 𝘴𝘵𝘳𝘰𝘮𝘢 𝘢𝘯𝘥 𝘱𝘰𝘪𝘯𝘵𝘴 𝘵𝘰 𝘯𝘦𝘸 𝘸𝘢𝘺𝘴 𝘵𝘰 𝘳𝘦𝘴𝘵𝘰𝘳𝘦 𝘵𝘩𝘺𝘮𝘪𝘤 𝘧𝘶𝘯𝘤𝘵𝘪𝘰𝘯 𝘢𝘧𝘵𝘦𝘳 𝘥𝘢𝘮𝘢𝘨𝘦 𝘰𝘳 𝘢𝘨𝘪𝘯𝘨.

💡𝗧𝗮𝗸𝗲 𝗵𝗼𝗺𝗲 𝗺𝗲𝘀𝘀𝗮𝗴𝗲
 • Juvenile axolotl regenerates thymus de novo after complete thymectomy, restoring nodule morphology by 35 days post-thymectomy.
 • Single-cell RNA sequencing shows regenerated thymus reconstitutes thymic epithelial cells, T cells, and stromal niches; transplantation proves renewed hematopoietic progenitor cell homing and thymopoiesis.
 • FOXN1 is essential for thymus size and T cell output, yet dispensable for rudiment initiation; MDK (midkine–protein tyrosine phosphatase receptor type Z1) signaling is an early regeneration trigger.

🔥𝗜𝗺𝗽𝗮𝗰𝘁
 • Defines a regeneration-specific midkine axis that could be harnessed to rebuild thymic epithelial niches after thymectomy or involution.

❓𝗢𝗽𝗲𝗻 𝗾𝘂𝗲𝘀𝘁𝗶𝗼𝗻𝘀
 • What is the lineage source of de novo thymic epithelial cells?
 • Can midkine activation restore mammalian thymus after complete ablation?
 • How is self-tolerance enforced without clear corticomedullary architecture?

𝗠𝗼𝗹𝗲𝗰𝘂𝗹𝗮𝗿 𝗯𝗮𝘀𝗶𝘀 𝗳𝗼𝗿 𝗱𝗲 𝗻𝗼𝘃𝗼 𝘁𝗵𝘆𝗺𝘂𝘀 𝗿𝗲𝗴𝗲𝗻𝗲𝗿𝗮𝘁𝗶𝗼𝗻 𝗶𝗻 𝗮 𝘃𝗲𝗿𝘁𝗲𝗯𝗿𝗮𝘁𝗲, 𝘁𝗵𝗲 𝗮𝘅𝗼𝗹𝗼𝘁𝗹
Anna Czarkwiani, Macrina Lobo, Lizbeth Bolaños-Castro, Ph.D. et al.
Science Immunology, December 2025
Corresponding author(s): Rene Maehr, Max H Yun

🔗 𝘓𝘪𝘯𝘬 𝘵𝘰 𝘵𝘩𝘦 𝘱𝘢𝘱𝘦𝘳 𝘪𝘯 𝘤𝘰𝘮𝘮𝘦𝘯𝘵𝘴
🧩 𝘐𝘭𝘭𝘶𝘴𝘵𝘳𝘢𝘵𝘪𝘰𝘯 𝘢𝘥𝘢𝘱𝘵𝘦𝘥 𝘧𝘳𝘰𝘮 𝘵𝘩𝘦 𝘱𝘢𝘱𝘦𝘳 + 𝘚𝘤𝘪𝘦𝘯𝘤𝘦 𝘐𝘮𝘮𝘶𝘯𝘰𝘭𝘰𝘨𝘺 𝘤𝘰𝘷𝘦𝘳 + 𝘮𝘺 𝘤𝘩𝘪𝘭𝘥𝘳𝘦𝘯'𝘴 𝘧𝘢𝘷𝘰𝘶𝘳𝘪𝘵𝘦 #𝘮𝘪𝘯𝘦𝘤𝘳𝘢𝘧𝘵 𝘤𝘩𝘢𝘳𝘢𝘤𝘵𝘦𝘳!

One of the most clinically useful aging markers is hiding in plain sight.
And it isn’t found in your genome.

At the Geneva Longevity Summit, I sat beside two pioneers Steve Horvath and Gordan Lauc, whose work has reshaped how we think about biological time.

The discussion made something very clear:

We are entering the era of immune-aging clocks, and IgG glycans are leading the way.

For decades, we assumed the genome held the answers to lifespan and disease risk.
But the data tells a different story.

Genetics explains only 10-30% of the variance in chronic disease and longevity. The rest comes from the biological systems that change in response to life: epigenetics, metabolism, immune signaling, and inflammation.

That’s where glycans come in.

Glycans are complex sugar structures attached to proteins. They regulate immunity, inflammation, and communication between cells. And because most plasma proteins (including IgG) are glycosylated, the IgG glycome becomes a real-time map of immune aging.

Here is why this matters clinically:

• IgG glycans shift predictably with age.
• This remodeling contributes directly to inflammaging.
• Pro-inflammatory patterns rise. Anti-inflammatory patterns fall.
• Women experience an accelerated shift during perimenopause due to estrogen loss.
• GlycanAge correlates strongly with frailty, metabolic dysfunction, and cardiovascular risk.

And unlike genetics, glycan profiles are reversible.

Lifestyle, sleep, exercise, nutrition, stress load, and hormone therapy, especially estradiol in menopausal women, can all modify glycan age.

Glycans reflect immune balance over weeks to months, are stable enough for clinical decisions, and responsive enough for intervention tracking.

Multiple clinics are piloting GlycanAge alongside lipid panels and HbA1c.

What would you do with a clearer window into your own immune age?

References:
Glycosylation: mechanisms, biological functions and clinical implications. (2024) 
Recent advances in N-glycan biomarker discovery among human diseases. (2024). 
| 25 comments on LinkedIn

Architecture of the neutrophil compartment

- Millions of neutrophils are produced every day by the bone marrow through a well-defined series of differentiation steps before their release into the circulation as terminally differentiated, non-proliferative cells that eventually infiltrate most tissues.

- Neutrophils exhibit remarkable phenotypic and functional diversity across tissues and disease, yet the lack of understanding of how this immune compartment is globally organized challenges translation to the clinic.

- Here the authors performed single-cell transcriptional profiling of neutrophils spanning 47 anatomical, physiological and pathological scenarios to generate an integrated map of the global neutrophil compartment in mice which was named NeuMap.

- NeuMap reveals that neutrophils organize in a finite number of functional hubs that distribute sequentially during maturation to then branch out into interferon-responsive and immunosuppressive states, as well as a functionally silent state that dominates in the healthy circulation.

- TGFβ, IFNβ and GM-CSF push neutrophils along the different trajectories, while transcription factor JUNB controls angiogenic and immunosuppressive states and promotes tissue revascularization.

- The architecture of NeuMap appears to be conserved across sex, environmental and genetic backgrounds, as well as in humans.

- Limitation of the study: relatively small number of pathophysiological conditions analysed. Perturbations associated with allergy, autoimmunity, mucosal inflammation or diseases associated with old age as well as developmental processes remain uncharted in NeuMap.

-  This study delineates the global architecture of the neutrophil compartment and establishes a framework for exploration and exploitation of neutrophil biology.

https://lnkd.in/eh-hw66V

#immunology #science #singlecell #omics

Stanford scientists have discovered that cancer cells don’t just use one trick to hide from the immune system—they use two separate “don’t-eat-me” signals to stop macrophages from killing them.

The first signal, CD47, was already famous for acting like an invisibility cloak that tells macrophages to back off, and blocking it with an anti-CD47 antibody is already in human trials.

In the Nature Immunology paper, the same Stanford team also found that tumors use MHC class I as a second stop signal by binding to a macrophage receptor called LILRB1, which suppresses the macrophage’s ability to engulf and destroy the cancer.

When researchers blocked both CD47 and LILRB1 in mice, tumors rapidly filled with immune cells, shrank significantly, and became far easier for the body to clear.

This shows that many cancers survive by running two overlapping escape systems, and turning off both “don’t-eat-me” pathways at once may dramatically boost the immune system’s ability to attack and eliminate tumors. | 17 comments on LinkedIn

Epigenetic and metabolic programming of innate immune cells shapes host defense and disease susceptibility.

Venez découvrir en avant première notre Livret d'Immunologie sur notre stand, ouvrage à destination des élèves en primaire. Il sera bientôt disponible sur notre site internet et sera distribué gratuitement aux enfants par les ambassadeurs de l'immunologie, qui présentent notre belle discipline, à l'occasion de la journée de l'immuno (qui est le 29 avril).

SFI Société Française d'Immunologie
#Immunologie
#vulgarisation
#science
#livre
#systèmeimmunitaire

TIMC Lab
Université Grenoble Alpes | 18 comments on LinkedIn

Immunometabolism, the intersection of cellular metabolism and immune function, has revolutionized our understanding of T cell biology. Changes in cellular metabolism help guide the development of thymocytes and the transition of T cells from naive to effector, memory and tissue-resident states. Innate-like T cells are a unique group of T cells with special characteristics. They respond rapidly, reside mainly in tissues and express T cell receptors with limited diversity that recognize non-peptide antigens. This group includes invariant natural killer T (iNKT) cells, mucosal-associated invariant T (MAIT) cells and some populations of γδ T cells. Different subsets of innate-like T cells rely on specific metabolic pathways that influence their differentiation and function and distinguish them from conventional CD4+ and CD8+ T cells. Although there are differences between innate-like T cell types, they share metabolic and functional features. In this Review, we highlight recent research in this emerging field. Understanding how metabolic programmes differ between innate-like T cells and other T cells may open opportunities for tailoring innate-like T cell responses and adoptive T cell therapies for use in cancer, metabolic and autoimmune diseases. Functional and metabolic properties of innate-like T cells — namely, iNKT cells, MAIT cells and some γδ T cells — differ from those of conventional T cells. This Review describes how metabolic pathways support innate-like T cell properties such as acquisition of effector capability in the thymus, rapid responsiveness, tissue persistence, antigen adaptation and functional flexibility.

The Nobel Prize in Physiology or Medicine 2025 was awarded to Mary E. Brunkow, Fred Ramsdell and Shimon Sakaguchi “for their discoveries concerning peripheral immune tolerance.”

Since the discovery of the segmented shape of the neutrophil nucleus, scientists have pondered its physiological relevance. Yet, to this day, neither the functional relevance nor the molecular mechanisms underlying the segmentation of the neutrophil nucleus are fully understood. Some experimental evidence supports a role of nuclear segmentation in efficient neutrophil migration but its impact on key neutrophil functions, such as phagocytosis, degranulation or production of reactive oxygen species, remains unclear. Nonetheless, the role of nuclear shape in remodelling chromatin and regulating gene expression has high potential for biological and translational relevance. This Review aims to compile and connect the current studies on the neutrophil nucleus, while also discussing studies in other cell types that could inform us about the relevance or mechanisms of nuclear segmentation. In this Review, the authors consider a long-standing immunological conundrum — why do neutrophils have a segmented nucleus? They discuss the mechanisms that may underlie segmentation of the neutrophil nucleus and explain how nuclear segmentation may affect neutrophil functions, including migration and phagocytosis.

The process of phagocytosis creates intracellular compartments (organelles known as phagosomes) that are central hubs for innate immune sensing of potentially dangerous microorganisms, cells, cellular debris and foreign objects. Receptors, enzymes and signalling molecules are specifically enriched in these compartments, wherein they learn everything they can about the phagocytosed material and signal for the cell to mount appropriate responses. The phagosome organelle is also a compartment that facilitates nutrient and metabolite harvesting from internalized materials. This Review explores recent developments in our understanding of phagocytosis as a specific mechanism of innate immune sensing. We discuss efforts to identify the catalogue of proteins that are enriched in different types of phagosomes to learn how these molecules work together to tailor inflammatory and antimicrobial immune responses. In this Review, Li and Underhill discuss recent advances in understanding the process of phagocytosis. The authors highlight how phagocytosis is integral for innate immune sensing and explain how the phagocytosed material itself shapes the phagocytosis process.

🚀 New preprint: A single-cell cytokine dictionary of human peripheral blood

Excited to share our new preprint, “A single-cell cytokine dictionary of human peripheral blood”.

In this work, we generated the Human Cytokine Dictionary:
👉 9.7 million single-cell transcriptomes across
👉 12 human PBMC donors and
👉 90 individual cytokine stimulations,
👉 by far the largest single-cell perturbation dataset from primary human immune cells to date.

This dataset lets us systematically map how human immune cell types respond to cytokines, uncover cell type–specific activities, donor-specific vs consensus responses, cytokine similarity groups, and higher-order cytokine-cytokine and cell-cell communication networks. A particularly interesting story is the IL-32-β–initiated cascade that rewires myeloid programs from antiviral/Th1-type responses towards a neutrophil-driven, IL-10–modulated inflammatory state.

To make this resource broadly usable, we also introduce huCIRA (Human Cytokine Immune Response Analysis), a Python package that
• exposes cytokine-induced gene and program signatures, and
• allows researchers to decode cytokine activity in their own single-cell and spatial transcriptomic datasets.
We showcase this on datasets from systemic lupus erythematosus, multiple sclerosis, and NSCLC.

Huge congratulations and thanks to our four co–first authors Lukas Oesinghaus, Sören Becker, Larsen Vornholz and Efi Papalexi,👏 for driving this enormous effort.

This project was only possible thanks to a fantastic collaboration with Parse Biosciences, leveraging their GigaLab platform to reach this unprecedented data scale, and to the Seelig lab for a truly inspiring and fun partnership across engineering, computation, and immunology.

I also want to thank Nir Hacohen and colleagues for their pioneering mouse Immune Dictionary (Cui et al., Nature 2024), which provided a key conceptual and analytical reference point for our human cytokine dictionary.

You can read the preprint here:
🔗 https://lnkd.in/gFB3NAdC

Looking ahead, I hope this work can serve as a blueprint for analyzing the many large-scale perturbation datasets to come - as both a biological reference and a testbed for virtual cell models of cytokine biology.
🔧 Code & huCIRA package: https://lnkd.in/g7cMPic3
🧰 For broader single-cell perturbation analysis, also check out pertpy in the scverse ecosystem: https://lnkd.in/g_7cpUfH

Looking forward to feedback, reuse of the Human Cytokine Dictionary and huCIRA by the community. | 13 comments on LinkedIn

Immunology is the most human—and the most beautiful—of disciplines. Thanks to B Andrade and M Araujo-Pereira for this very pertinent parallel.

This recent PNAS paper is making headlines. Why? Because it focuses on something extremely familiar - Tattoos!

Researchers explored how tattoo ink interacts with the immune and lymphatic systems and clearly demonstrated that its effects do not occur only at the tattoo's site. Instead, it can have a significant, long-term impact on the draining lymph nodes, which affect immune responses to events like vaccines and potentially many other situations as well.

Particularly relevant in a world where nearly 1 in 3 people is likely to have at least a tattoo. And a great example of how science can talk so directly to the general public when it feels familiar. 

If you want to even begin to really understand how cells work, you need to watch this video first; and then reread all the static imagery text books of biochemistry & molecular biology again with fresh eyes. Excellent video Simon Reid.
#highereducation

A roadmap for defining “extrafollicular” B cell responses

Long-lived plasma cells (LLPCs), which continuously secrete antibodies, play a central role in humoral immunity and form the foundation of effective vaccin