Team Leader
TEAM LEADER : Alexandre Loupy
Mail : alexandre.loupy@inserm.fr
Localisation : Lab 359 – 3rd floor
DOCTORAL SCHOOL : ED 562 – BIO SCIENCE PARIS CITE – Université PARIS CITE
The Paris Transplant Group is part of the PARCC and the PITOR institute (Paris Transplantation & Organ Regeneration Institute). It is dedicated to improving patient management and outcomes through the development and validation of AI prediction models, new technologies for advanced monitoring, and xenotransplantation. We connect immunologists, laboratory medical practitioners, researchers, nephrologists, cardiologists, pneumologists, hepatologists, pediatricians, pathologists, public health specialists, bioinformaticians, data managers, data analysts and AI specialists to foster innovation, collaboration, and excellence in patient care.
Our vision is to build the future of precision transplantation medicine by integrating clinical, biological, and technological innovations to improve patient outcomes, expand therapeutic possibilities, and strengthen the continuum between research and clinical practice.
Our main objectives are:
Support innovation across the entire transplantation value chain, from organ preservation to regeneration.
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More information on our website
Our main topics are:
#1 Developing the first AI Transplant Clinic
We are developing the prototype of the first AI Transplant Clinic (AITC), a groundbreaking initiative that is redefining transplant care by embedding advanced artificial intelligence directly into clinical workflows.
At its core, the AITC builds a dynamic digital twin for each patient, enabling real-time and personalized management. The clinic is being structured into specialized departments: organ allocation, precision diagnostics, prognostication, non-invasive monitoring, simulation, data integration, and AI research, each powered by validated AI innovations emerging from our team. Among these innovations are the iBox prognostic model, the Virtual Biopsy System, the Banff Automation System, and donor-derived cell-free DNA-based liquid biopsy. These tools enhance precision, reduce invasive procedures, and support data-driven clinical decisions.
The AITC also introduces new healthcare roles, such as digital clinicians and AI specialists, who work in synergy with traditional medical teams. Its architecture is supported by agentic AI systems, which are autonomous, reasoning agents that orchestrate data access, clinical communication, and interactions with predictive models. These agents ensure seamless integration between human decision-makers and the AI infrastructure, making the AITC a truly adaptive and intelligent ecosystem.
Through ongoing pilot implementations and real patient cases, the clinic demonstrates how AI-driven medicine enables proactive, personalized interventions and the simulation of treatment scenarios before they are applied in practice.
By developing the AITC, we are laying the foundations for a new era of AI-integrated, precision medicine, one that can extend far beyond transplantation to transform the care of complex diseases.
#2 The iBox prediction system
iBox is a decision support algorithm that integrates several types of variables: biological, histological, and immunological data, with the aim of predicting medium/long-term kidney transplant survival. This tool improves quality of life and graft survival through more detailed and personalized monitoring, as well as optimization of medical resources (better organ allocation, adaptation of care). It is now recognized by European Medecines Agency as a predictive medicine tool in kidney transplantation (and is being rolled out for other organs) and received favorable opinion as a prediction tool by the US Food and Drug Administration (FDA).
In our team, the iBox is used as a risk stratification platform: it allows us to identify, from the post-transplant period onwards, transplant patients at increased risk of graft loss. It will also accelerate therapeutic innovation in transplantation by reducing the duration or size of clinical trials through a valid predictive tool.
We are working on integrating “omic” data, non-invasive biomarkers (cfDNA, etc.), and detailed immunology to enhance the predictive performance of iBox. We are also in the process of transposing the application to heart and lung transplants, as part of the “multi-organ transplant” dimension of our cohort.
#3 : Non-invasive monitoring of rejection with donor-derived cell-free DNA:
Organ transplant monitoring traditionally involves biopsies, immunological, histological, and functional analyses. However, these approaches are often invasive, sometimes delayed, or insensitive to certain early mechanisms of rejection or graft damage. The use of donor-derived cell-free DNA (dd-cfDNA) as a non-invasive biomarker of graft health is an innovative solution that allows:
Within our cfDNA platform, established in 2022, we have phenotyped more than 5,000 samples and integrated them into cohort studies with a view to early detection of graft rejection or dysfunction, to improve monitoring and management. We combine this approach with other markers (functional, immunological, histological) to develop multimodal predictive models.
#4 Xenotransplantation :
The shortage of organs remains a major issue in solid organ transplantation. Xenotransplantation may be a way forward in addressing this challenge. However, this clinical application requires a thorough understanding of the highly complex immunological responses associated with xenotransplantation: xenogeneic immune rejection, species incompatibilities, new infectious risks, etc.
Our ambition is, in collaboration with the NYU Langone Health Hospital, to decipher the mechanisms of the xenogeneic immune response, identify predictive signatures of rejection or dysfunction in this context, and contribute to the translation to human trials. In this process, we want to adapt our “precision diagnosis” approach to allografts to xenotransplantation, which involves implementing multimodal phenotyping of xenografts: histology, gene expression, immunology, non-invasive biomarkers, etc.
This will not only provide additional options for patients awaiting transplants but also advance fundamental research on the mechanisms of rejection, chronic inflammation, and inter-species immune tolerance.
Through these areas of focus, our team aims to push the boundaries of solid organ transplantation: not only by refining risk stratification and allograft management, but also by preparing for the arrival of new solutions (xenografts) to address the organ shortage.
We combine ambitious translational research (cohorts, biomarkers, advanced statistics) with a strong clinical focus and a vision of personalized medicine.
Team Leader
Scientific Leader
Project Manager
Director of Partnership
Platform Manager
Platform Manager
Project Manager
Data Manager
Scientist
Clinician
Clinician
Clinician
Clinician
Post-doctoral fellow
PhD Student
PhD Student
Phd Student
Post-doctoral Fellow
Post-doctoral Fellow
Post-doctoral fellow
Post-doctoral Fellow
Phd Student
Post-doctoral Fellow
Platform Manager
Technician
Technician
Technician
Clinical Research Associate
clinical research assistant
clinical research assistant
clinical research assistant
Clinical Research Associate
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Affiliated Clinicians, Surgeons and Researchers
Team Awards
Team Fundings
This project merges research in transplantation, artificial intelligence, and regenerative medicine to efficiently address organ failures, shortage of donors, and transplant patient care.
This project aims at developing innovating diagnostic tools in xenotransplant. To better characterize the xenoimmune response, optimize the genetically modified pig models, guide the choice of immunosuppressive treatments and accelerate future clinical trials of xenotransplant in humans.
Link to the xenotransplant project website : https://www.msdavenir.fr/projet-xenotransplant/
This project aims at developing integrative AI-based systems for non-invasive monitoring, precision medicine and rejection diagnosis improvement in kidney transplantation.
This project aims at developing a prognostic system to personalize pharmacological approaches in congestive heart failure.
Link to the H2020 Biotool-CHF project website : https://www.biotool-chf.eu/
This project aims at analyzing the factors that have influenced the organ procurement processes before, during and after the onset of SARS-CoV2 pandemic to propose sustainable innovative actions directed at improving the resilience of the donation and transplant systems and networks to favor a more equitable access to transplantation for all patients with end-stage organ disease.
Link to the H2020 Eu4health BRAVEST project website : https://www.bravest-project.eu
Engineering a diagnostic system for precision medicine in kidney transplantation. This project aims at providing a solid algorithm tool to the clinician for diagnosis in the context of kidney transplantation by combining all the pertinent information currently available in patient’s follow-up. The project was funded by the French ANR (National Research Agency) and the consortium involves 7 French referral transplant centres and 2 industrial partners.
Link to the ANR related webpage here
Link to the KTD-innov website here
The goal of this project is to develop an integrated risk-stratification and prognosis system (EU-TRACER) to improve graft survival in kidney transplantation. This system will be converted into clinical actionable information for the clinician to monitor individual risk prediction (3, 5, 7, 10-year allograft loss) and in patients with high-risk of rejection to get a probability of response to standard of care treatment and impact on outcomes. The project was funded by the European Commission and the EU-TRAIN consortium involves 7 European transplant centres and 2 industrial partners.
Link to the EC related webpage here
Link to the EU-TRAIN website here
Loupy A, Preka E, Chen X, Wang H, He J, Zhang K. Nat Med. 2025 Jul;31(7):2161-2173. doi: 10.1038/s41591-025-03801-9. Epub 2025 Jul 14. PMID: 40659768.
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Loupy A, Sablik M, Khush K, Reese PP. Lancet. 2025 Jul 26;406(10501):389-402. doi: 10.1016/S0140-6736(25)00195-3. Epub 2025 Jul 1. PMID: 40614744.
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Goutaudier V, Aubert O, Racapé M, Truchot A, Sablik M, Raynaud M, Vicaut É, Rousseau O, Elias M, Divard G, Papuchon E, Danger R, Charreau B, Bouton D, Nguyen-Khoa T, Randoux-Lebrun C, Taupin JL, Gourraud PA, Giral M, Le Quintrec M, Morelon E, Couzi L, Legendre C, Lefaucheur C, Kamar N, Brouard S, Anglicheau D, Loupy A; KTD-Innov Consortium. J Am Soc Nephrol. 2025 Jun 12. doi: 10.1681/ASN.0000000742. Epub ahead of print. PMID: 40504617.
Juric I, Raynaud M, Skoric L, Al-Awadhi S, Truchot A, Sablik M, Ma X, Lv K, Zhang H, Louis K, Basic-Jukic N, Tissier R, Hauet T, Cozzi E, Oniscu GC, Mangiola M, Tector JA, Riella LV, Locke JE, Samuel D, Meier RPH, Mohiuddin MM, Montgomery RA, Loupy A. Xenotransplantation. 2025 May-Jun;32(3):e70058. doi: 10.1111/xen.70058. PMID: 40551623.
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Raynaud M, Bakker SJL, Bentall AJ, Loupy A. Kidney Int. 2025 Mar;107(3):568. doi: 10.1016/j.kint.2024.11.015. PMID: 39984257.
Cortes Garcia E, Giarraputo A, Racapé M, Goutaudier V, Ursule-Dufait C, de la Grange P, Adoux L, Raynaud M, Couderau C, Mezine F, Dagobert J, Bestard O, Moreso F, Villard J, Halleck F, Giral M, Brouard S, Danger R, Gourraud PA, Rabant M, Couzi L, Le Quintrec M, Kamar N, Morelon E, Vrtovsnik F, Taupin JL, Snanoudj R, Legendre C, Anglicheau D, Budde K, Lefaucheur C, Loupy A, Aubert O. Transpl Int. 2024 Jul 10;37:13043. doi: 10.3389/ti.2024.13043. PMID: 39050190; PMCID: PMC11267505.
Aubert O, Ursule-Dufait C, Brousse R, Gueguen J, Racapé M, Raynaud M, Van Loon E, Pagliazzi A, Huang E, Jordan SC, Chavin KD, Gupta G, Kumar D, Alhamad T, Anand S, Sanchez-Garcia J, Abdalla BA, Hogan J, Garro R, Dadhania DM, Jain P, Mandelbrot DA, Naesens M, Dandamudi R, Dharnidharka VR, Anglicheau D, Lefaucheur C, Loupy A. Nat Med. 2024 Aug;30(8):2320-2327. doi: 10.1038/s41591-024-03087-3. Epub 2024 Jun 2. PMID: 38824959; PMCID: PMC11333280.
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Yoo D, Divard G, Raynaud M, Cohen A, Mone TD, Rosenthal JT, Bentall AJ, Stegall MD, Naesens M, Zhang H, Wang C, Gueguen J, Kamar N, Bouquegneau A, Batal I, Coley SM, Gill JS, Oppenheimer F, De Sousa-Amorim E, Kuypers DRJ, Durrbach A, Seron D, Rabant M, Van Huyen JD, Campbell P, Shojai S, Mengel M, Bestard O, Basic-Jukic N, Jurić I, Boor P, Cornell LD, Alexander MP, Toby Coates P, Legendre C, Reese PP, Lefaucheur C, Aubert O, Loupy A. Nat Commun. 2024 Jan 16;15(1):554. doi: 10.1038/s41467-023-44595-z. PMID: 38228634; PMCID: PMC10791605.
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Cortes Garcia E, Giarraputo A, Racapé M, Goutaudier V, Ursule-Dufait C, de la Grange P, Letourneur F, Raynaud M, Couderau C, Mezine F, Dagobert J, Bestard O, Moreso F, Villard J, Halleck F, Giral M, Brouard S, Danger R, Gourraud PA, Rabant M, Couzi L, Le Quintrec M, Kamar N, Morelon E, Vrtovsnik F, Taupin JL, Snanoudj R, Legendre C, Anglicheau D, Budde K, Lefaucheur C, Loupy A, Aubert O. Transplantation. 2025 May 1;109(5):871-880. doi: 10.1097/TP.0000000000005181. Epub 2024 Oct 23. PMID: 40261978.
Demir Z, Raynaud M, Aubert O, Debray D, Sebagh M, Duong Van Huyen JP, Del Bello A, Jolivet NC, Paradis V, Durand F, Muratot S, Lozach C, Chardot C, Francoz C, Kamar N, Sarnacki S, Coilly A, Samuel D, Vibert E, Féray C, Lefaucheur C, Loupy A. Am J Transplant. 2024 Jun;24(6):954-966. doi: 10.1016/j.ajt.2023.12.007. Epub 2023 Dec 12. PMID: 38097016.