Erin McCaffrey, PhD
@erin-mccaffrey.bsky.social
170 followers 250 following 29 posts
Principal Investigator of the Spatial Immunology Unit | Independent Research Scholar | NIH/NIAID Intramural Research Program Spatially mapping the immune ecosystem of infection and inflammation (Views are my own)
Posts Media Videos Starter Packs
Reposted by Erin McCaffrey, PhD
charliejpyle.bsky.social
You can now explore the mRNA expression of your favorite TB gene of interest in our recently published human pulmonary M.tb granuloma single-cell dataset at the Broad Single Cell PORTAL!

@broadinstitute.org
@wallacewly.bsky.social

singlecell.broadinstitute.org/single_cell/...
Paired single-cell and spatial transcriptional profiling reveals a central osteopontin macrophage response mediating tuberculous granuloma formation - Single Cell Portal
Granulomas are classic manifestations of tuberculosis pathogenesis. They result from an ensemble of immune responses to Mycobacterium tuberculosis infection, but the identities, arrangement, cellular interactions, and regulation of the cells that comprise them have thus far been incompletely understood. To better understand the composition of granulomas, we conducted spatial and single-cell RNA sequencing of granulomas in biopsy specimens from patients with tuberculosis. We found that granulomas consist of concentric transcriptional laminae surrounding areas of central necrosis. We identified distinct populations of granuloma-associated stromal cells, fibroblasts, lymphocytes, mast cells, dendritic cells, neutrophils, and macrophages. Furthermore, gene expression among these cell populations differed by location within granulomas. We used inferential analysis to predict dominant granuloma cell-cell interactions, the activity of major signaling pathways, and transcription factor activities. Using spatial deconvolution, we mapped a conserved pattern of cellular organization dominated by macrophages rich in SPP1/osteopontin expression. Trajectory analysis of macrophage subtypes mapped their differentiation and supported the importance of SPP1 to granuloma macrophage polarization. Using the Mycobacterium marinum-zebrafish model, we found that mycobacterial infection induces spp1 expression in macrophages and that spp1 ablation results in granuloma formation defects and reduced survival in adult animals. Cumulatively, we have identified a dominant macrophage granuloma population as well as its central regulatory gene in human samples and confirmed the importance of spp1 to granuloma biology in vivo.
singlecell.broadinstitute.org
Reposted by Erin McCaffrey, PhD
bengern.bsky.social
I’m excited to announce that our paper, describing early and opposing roles for neutrophils and CD4 T cells in determining #TB lesion structure, is out at @jem.org ! Huge thanks to my lab, and the Urdahl, @michael-gerner.bsky.social, and Aitchison labs who made this possible

doi.org/10.1084/jem....
Reposted by Erin McCaffrey, PhD
thebrysonlab.bsky.social
Newest paper from the lab out today (doi.org/10.1084/jem....)! Here, we describe PathMHC, a novel MS-based approach to identify rare pathogen-derived peptides on MHC-I and MHC-II. We apply this to a range of pathogens Mtb, SARS-CoV-2, and Listeria.
Targeting infection-specific peptides in immunopeptidomics studies for vaccine target discovery
MS-based immunopeptidomics can facilitate vaccine antigen discovery, but self-MHC peptides greatly outnumber pathogen-derived MHC peptides, presenting a ch
doi.org
erin-mccaffrey.bsky.social
I also had never seen this format until our preprint was reviewed. Seems to be mostly preprint-focused. Anyways, thanks for sharing the biorxiv link 😊
Reposted by Erin McCaffrey, PhD
danbarberphd.bsky.social
We are looking for post-docs interested in studying T cell responses to M. tuberculosis infection…especially basic T cell immunologists who are interested in learning to work with BSL3 pathogens. The NIH intramural program is an amazing place to train!
Reposted by Erin McCaffrey, PhD
sarasuliman.bsky.social
It's world TB day.

The last two months have been a series of attacks on global health, infectious disease science and vulnerable populations. The damage will take decades to undo, and we are heading onto a steep global health disaster.

We can't stay quiet.
#tuberculosis #TB #WTBD2025
Reposted by Erin McCaffrey, PhD
tomscriba.bsky.social
Today is the 24th of March and it's World TB Day. We typically have many activities to educate and raise awareness about TB and how important it is for us all to commit to doing more to end TB! This year feels different though.
Reposted by Erin McCaffrey, PhD
Reposted by Erin McCaffrey, PhD
johngreensbluesky.bsky.social
I recommend hating tuberculosis. It has fueled me like no other hate that came before.
erin-mccaffrey.bsky.social
Thank you Alissa! Moving, starting up the lab, and getting this submitted felt like an extreme sport 😅 Very grateful to have a supportive community at NIH and the always inspiring early career TB research crew to look up to (like you 😉)

P.S. SO bummed I couldn't be at KS to catch up!
erin-mccaffrey.bsky.social
But microbial factors could be at play. Especially since we know Mtb resides in the caseum and prompts macrophage necrosis. We are hoping some of our organoid work will help us decouple the chicken-and-egg relationship between hypoxia and bacterial burden.
erin-mccaffrey.bsky.social
This is a great question. To try to get at it, we are currently evaluating granulomas from an earlier timepoint of infection. These grans have much higher CFU but less hypoxia. The main thrust of hypoxia appears to be caseation and it may be exacerbated by the degree of neutrophil influx...
erin-mccaffrey.bsky.social
Thank you! We are excited to finally be able to share it with everyone.
erin-mccaffrey.bsky.social
Thanks for tuning in! Please feel free to reach out with any feedback or questions on our preprint. (20/20)
erin-mccaffrey.bsky.social
The senior authors on this paper (especially my PhD advisor, Mike Angelo) have been the most incredible mentors to me and the wind behind my sails as I transitioned from Stanford to the NIH to start my own group. Despite...everything 🙃...I am excited for the cool science we are cooking up! (19/20)
erin-mccaffrey.bsky.social
In Nov 2023 I started my lab at the NIH (the Spatial Immunology Unit) as an Independent Research Scholar. We are combining spatial mapping of tissues with functional assays in organoid models to define the principles of immune programming during infection and inflammation with a focus on TB. (18/20)
erin-mccaffrey.bsky.social
A HUGE thank you my co-author, Alea Delmastro, who began as my undergrad mentee in 2018, adapted MIBI for NHP tissues (no small feat), and then became my co-lead on this study. Here we are celebrating after we stained the study cohort during the pandemic (a culmination of 3 years of work). (17/20)
erin-mccaffrey.bsky.social
I would like to thank the extremely creative, talented, and hard-working individuals who worked on this study. This team spans 8 institutions and much of this work was done in the depths of the pandemic. I am so grateful for their brilliance, collaboration, and friendship. (16/20)
erin-mccaffrey.bsky.social
Moral of the story? Granuloma hypoxia is associated with pathologic immune cell states, dysfunctional cellular organization of the granuloma, and a near-complete blockade of lymphocyte infiltration that would be required for a successful host response. (14/20)
erin-mccaffrey.bsky.social
Lastly, we confirmed that the same phenomenon of immunometabolic zonation is present in human pulmonary TB, underscoring the translational relevance of our findings. (13/20)
erin-mccaffrey.bsky.social
We also applied QUICHE (from the talented Jolene Ranek in the Angelo lab) to map the spatial networks of low- versus high-bacterial burden granulomas. With this analysis we found that hypoxia-associated spatial niches were over-represented in high-bacterial burden granulomas. (12/20)