MD/PhD student @uabmstp | @jamesgeorgeuab & @anupamuab labs | slu grad | amateur cook | tweets my own | he/him

Birmingham, AL
Joined June 2016
FINALLY OUT! Our work using spatial and single-cell transcriptomics to characterize the human immune response in pig-to-human kidney xenotransplantation is now published @NatureComms 🧵 nature.com/articles/s41467-0…
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Halloween on peds is the best! Rounding as a giraffe this morning
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As a med student who had 2 children during med school I'm often asked what kind of support I need, and besides the obvious like childcare, I never had a good answer. This elective at the University of Minnesota is the definition of support, all med schools should take notes.
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The 3rd Acute Kidney Injury: Bench to Bedside conference is coming May4-7,2025! Save the date! Great program plus an awesome Workforce development program for trainees! Travel awards, lots of great science and networking in beautiful Leesburg Virginia👇
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Matthew Cheung retweeted
Limited infiltration of host immune cells in the very first case of 10-gene-edited pig-to-human (brain-dead) Kidney #Xenotransplant <=74 h Minimal B/T lymphocytes CD45+ cells are mainly donor-derived M2-like macrophages, plus neutrophils Love to see more analysis on endothelial/epithelial compartment (Another paper in progress?) #SpatialTranscriptomics #Visium sc- & sn-RNAseq #cell2location Distinguishing Pig vs Human transcripts/cells Paige Porrett lab @NatureComms 2024 @MatthewDCheung nature.com/articles/s41467-0…
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Matthew Cheung retweeted
Congratulations to outstanding MDPhD students - now Drs. Matthew Cheung and Gelare Ghajar-Rahimi, who successfully defended their theses. It was my honor to serve as co-mentor with Jim George. ⁦@UABMSTP⁩ ⁦@UABHeersink⁩ ⁦@MatthewDCheung⁩ ⁦@G_GhajarRahimi⁩
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PhDone!!!! Thank you to my amazing friends, family, colleagues, and mentors - couldn't have done any of this without you!
My work son, @MatthewDCheung, just defended his PhD thesis at @uabmedicine and I am speechless. Matthew, you have accomplished so much in such a brief amount of time and I am so incredibly proud of you! ❤️🫘(these are the only kidneys I could find lol) @alhkim #AKI
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It's actually happening!!!! T-2 days
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What an incredible night celebrating the honorees of the @UABgsga Awards, alongside their mentors, family, and friends! We’re immensely proud of these recipients, their outstanding accomplishments & the positive impacts they’ve made on our academic community & beyond! #GoBlazers
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#TBT to a month ago when our @UABgsga’s Senior Associate Dean and Director of Graduate Biomedical Sciences, David Schneider, joined Mathew Cheung, the Three Minute Thesis (3MT®) UAB 1st place winner, in South Carolina for the southern regional 3MT® competition. 🔬🧫🧪
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Nonetheless, our data suggest that a standard immunosuppression regimen can control the immune response to the pig kidney, at least early on. Long term studies are needed. These data will still play a key role in propelling pig kidney xenotransplantation to a clinical reality.
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It really takes a village. Thank you to the entire UAB xenotransplant team for making this possible! As always, thank you to our donors and their families. And a shout out to my co-mentors (@AnupamUAB and Jim George) for letting me take part in this special project. Cheers!
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We did a co-localization analysis to see where these immune cells were found in the kidney. The neutrophils near endothelial cells may be contaminants (which would be good) or a response to the TMA. Interestingly, the human macrophages tended to localize with pig stromal cells
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Several study limitations: 1. n =1 (but stay tuned), 2. short-term, 3. tough to validate at protein level due to high cross-reactivity of pig/human antibodies, 4. hard to distinguish impact of gene edits vs pharmacologic interventions
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Now we know that in the kidney, these interactions tend to skew macrophages towards a more anti-inflammatory, pro-healing phenotype. And that's exactly what we see in both the pig and human macs when we looked at their gene expression profiles
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Human myeloid cells, however, infiltrated the pig kidney soon after xenotransplant
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To our reassurance, we found no presence of human B or T cells in the pig kidney biopsies (note, we had to use marker genes for B/T cells bc not in reference transcriptome)
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Knowing what immune cells were present in the explanted kidney, we wanted to track these over time. We performed @10XGenomics Visium spatial transcriptomics on the serial biopsies and used the sc/snRNAseq data to deconvolute the spatial data using cell2location
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We detected human neutrophils, monocytes, and macrophaes as well as pig T cells, neutrophils, and macrophages in the explanted pig kidney 3 days after xenotransplant.
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Problem: how do you identify what is a pig cell vs human cell in a mixed sample of pig/humancells? Solution: We built a merged pig-human reference genome to align our sequencing data to, so we could distinguish species and cell types. (Many more details/methods in the paper!)
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We collected biopsies from the pig kidneys both before and after transplant. We also sorted out pig and human immune cells from the explanted pig kidney and performed scRNAseq
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