Evidence mapPaperPMID 41006232Full record

ArticleNature communications2025

Physiologic Homeostasis in a Living Human after Pig Kidney Xenotransplantation.

Sul A Lee, Marie-Camille Lafargue, Winfred W Williams, Kassem Safa, Ragnar Palsson, Ayman Al Jurdi, Abraham Cohen-Bucay, Pitchaphon Nissaisorakarn, Hannah Gilligan, Harald Jüeppner and 11 more

Abstract readCase Reports
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Xenotransplantation in Nephrology: A Narrative Review.Journal of personalized medicine · 2026
    Review
  2. Urate metabolism in the gut.Life metabolism · 2026
    Article
  3. Review
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Sul A LeeDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0003-2121-721X
Marie-Camille LafargueCenter for Transplantation Sciences, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-9000-1207
Winfred W WilliamsDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Kassem SafaDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Ragnar PalssonDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Ayman Al JurdiDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Abraham Cohen-BucayDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4951-7070
Pitchaphon NissaisorakarnDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-0245-2954
Hannah GilliganDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Harald JüeppnerHarvard Medical School, Boston, MA, USA.
Leela MorenaCenter for Transplantation Sciences, Massachusetts General Hospital, Boston, MA, USA.
Thiago J BorgesCenter for Transplantation Sciences, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6554-0169
Mariesa A LeDivision of Pharmacy, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-5220-7228
Kayla F JoyalDivision of Pharmacy, Massachusetts General Hospital, Boston, MA, USA.
Eugene P RheeDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-4804-7583
Ivy RosalesHarvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-0621-3202
Thomas BrannonDivision of Nephrology and Hypertension, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jan WysockiDivision of Nephrology and Hypertension, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Daniel BatlleDivision of Nephrology and Hypertension, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Tatsuo KawaiCenter for Transplantation Sciences, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6900-4603
Leonardo V RiellaDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA. lriella@mgh.harvard.edu.ORCID http://orcid.org/0000-0002-7636-3196

Funding

Training CoreTL1DK143273 · BRIGHAM AND WOMEN'S HOSPITAL · 2025 to 2025
$1.5M
Division of Intramural Research, National Institute of Allergy and Infectious Diseases (Division of Intramural Research of the NIAID) R01AI143887NIAID NIH HHS R01 AI143887NIDDK NIH HHS TL1 DK143273U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) TL1DK143273
6 · The paper itself

Abstract

Kidney allotransplantation remains the preferred treatment for end-stage kidney disease, yet donor shortages limit its availability. Xenotransplantation using genetically modified porcine kidneys offers a promising alternative. Here, we report key physiological observations from the first-in-human porcine kidney xenograft over a 51 day postoperative follow-up period. The transplanted kidney maintained essential functions, including waste excretion, electrolyte regulation, and production of concentrated urine, while supporting blood pressure and sodium reabsorption despite reduced activation of the renin-angiotensin-aldosterone system. Sodium retention required diuretic therapy, and mild hypocalcemia and hyperphosphatemia occurred in the setting of pre-existing hypoparathyroidism. Markedly increased urinary uric acid excretion led to hypouricemia without evidence of urate nephropathy. This case demonstrates the ability of a porcine kidney to sustain vital metabolic functions in a living human, while highlighting areas for further research. These findings provide a foundation for optimizing post-transplant care and advancing xenotransplantation as a solution to the critical organ shortage.

Indexed as

HomeostasisKidneyKidney TransplantationTransplantation, HeterologousAnimalsAnimals, Genetically ModifiedHeterograftsHumansKidney Failure, ChronicMaleSodiumSwineSodium

Identifiers

PMID41006232
PMCPMC12474878

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.