Maximilian Heeg
@maximilian.heeg.io
120 followers 61 following 17 posts
Assistant Investigator at @alleninstitute.bsky.social | Former postdoc @GoldrathLab | Pediatrician | Interested in tissue resident memory T cells and Immunodeficiencies | Mountain enthusiast ⛰ | 🐕 #immunology Personal website: www.heeg.io
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maximilian.heeg.io
So proud to be a co-author on this study and absolutely loved the beautiful thread by @marionpepper.bsky.social — high recommended 👇
marionpepper.bsky.social
Asthma is a chronic disease characterized by acute, intermittent, recurrent episodes of airway inflammation. A decade of work developing the tools, techniques and collaborations needed to figure out how CD4+ T cells in the lungs propagate disease can be found here:
www.biorxiv.org/content/10.1...
Tertiary lymphoid structures support the development of allergen-specific progenitor CD4+ T cells
Tissue-resident memory CD4+ T cells (TRM) are key sentinels of the adaptive immune response that provide a rapid, robust inflammatory response upon reactivation in non-lymphoid tissues. While CD4+ TRM...
www.biorxiv.org
Reposted by Maximilian Heeg
labwaggoner.bsky.social
@biorxivpreprint.bsky.social Tertiary lymphoid structures support the development of allergen-specific progenitor CD4+ T cells @marionpepper.bsky.social
www.biorxiv.org/content/10.1...
Reposted by Maximilian Heeg
marionpepper.bsky.social
More coming on what this means but this was one of those stories that took almost a decade to come together but was well worth the time. Also check out a companion piece on @biorxiv by Patrick Brennan!
labwaggoner.bsky.social
@biorxivpreprint.bsky.social Tertiary lymphoid structures support the development of allergen-specific progenitor CD4+ T cells @marionpepper.bsky.social
www.biorxiv.org/content/10.1...
maximilian.heeg.io
📢 Join our team at @alleninstitute.bsky.social! We're hiring a Bioinformatics Scientist II for spatial transcriptomics in immunology.
Our latest work in Nature shows how tissue architecture shapes immune cell diversity. Now we're expanding our team!
Learn more: alleninstitute.org/careers/jobs...
Jobs
We are working to solve the biggest mysteries in bioscience.
alleninstitute.org
maximilian.heeg.io
Yes. The colors in the final row are unrelated. This shows Leiden Cluster and not cell types.
maximilian.heeg.io
The first three rows of Fig 1d are colored as indicated in the legend. Row 4 highlights the antigen specific T cells and row 5 is coloured by leiden clustering. If you want to explore the cell types I recommend having a look at the anndata object: www.ncbi.nlm.nih.gov/geo/query/ac...
maximilian.heeg.io
Thanks. Are you going to be in asilomar this weekend?
maximilian.heeg.io
I cannot believe you still have that picture! That's when all the fun started almost two years ago....
Reposted by Maximilian Heeg
erictopol.bsky.social
Spatial omics rides again, this time determining how immune CD8 T cells by location in the gut have different roles, such as killing function in the villus and backup reinforcements in the crypts
www.nature.com/articles/s41...
Good Explainer www.lji.org/news-events/...
@alleninstitute.bsky.social
Reposted by Maximilian Heeg
jem.org
New: Amir Ferry, Ananda Goldrath and colleagues @ucsdhealthsci.bsky.social show that differentiation of tissue-resident memory T cells (TRM) is accompanied by the upregulation of the conventional DC1 (cDC1) chemoattractant, Xcl1. https://buff.ly/4hrKCYe

#MucosalImmunology #TumorImmunology
Reposted by Maximilian Heeg
alleninstitute.org
When your gut is under attack, the immune system is activated. Like any good army, the roles of each cellular soldier depends on their location. 🧵

📸 Elena Lin/ @ucsdhealthsci.bsky.social

#ImmunoSky
maximilian.heeg.io
Beautiful thread on how tissue-resident T cells organize in the gut post-infection from my co-conspirator @reinacampos.bsky.social. Our spatial multi-omics work revealed unexpected complexity in immune system architecture. Think less checkers, more 4D chess 🧬🔬
Reposted by Maximilian Heeg
maximilian.heeg.io
🧵 9/10 Technical innovation: We developed a strategy for pooled optically encoded gene perturbations compatible with spatial transcriptomics, enabling mechanistic studies in situ
maximilian.heeg.io
🧵 8/10 Our spatial framework reveals that T cell location and functional state are fundamentally intertwined - establishing a new paradigm for understanding tissue immunity
maximilian.heeg.io
🧵 7/10 Importantly, we validated these findings in human tissue. Analysis of healthy human terminal ileum revealed similar spatial organization of CD8 T cell states
maximilian.heeg.io
🧵 6/10 TGFβ signaling proved essential for proper TRM positioning. TGFβRII KO cells showed impaired migration to the villus tip and reduced acquisition of tissue-residency programs
maximilian.heeg.io
🧵 5/10 Using CRISPR-based perturbations with spatial readout, we demonstrated that CXCR3 signaling is crucial for early positioning of effector cells. Loss of CXCR3 altered cellular positioning and subsequent differentiation fate
maximilian.heeg.io
🧵 4/10 This diversity is regulated by:
1. Distinct ligand-receptor activities
2. Spatial cytokine gradients
3. Specialized cellular contacts creating a complex molecular landscape that guides TRM differentiation
Specialized cellular contacts create a complex molecular landscape that guides TRM differentiation. Cells in the small intestine are colored by cell type and connected to their neighboring cells.
maximilian.heeg.io
🧵 3/10 Key finding: We identified two distinct TRM states defined by their location:
• Differentiated TRM cells (Gzma+, Gzmb+, Itgae+) in upper villus
• Progenitor-like TRM cells (Tcf7+, Slamf6+) in lower villus/crypt
maximilian.heeg.io
🧵 2/10 Using spatial transcriptomics (Xenium & MERSCOPE), we discovered that intestinal TRM cells occupy distinct niches that shape their phenotype and function. We developed computational approaches to map cells along three anatomical axes 📊
Each cell is colored according to its positions along the 3 main axes (crypt to villus, epithelial distance and longitudinal).