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Retrospective Cohort Study
Copyright ©The Author(s) 2026. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Transplant. Mar 18, 2026; 16(1): 111959
Published online Mar 18, 2026. doi: 10.5500/wjt.v16.i1.111959
Outcomes of basiliximab vs alemtuzumab induction in kidney allograft recipients with matched immunological Profiles: A retrospective cohort study
Chukwuma A Chukwu, Philip A Kalra, Marcus Lowe, Kay Poulton, Titus Augustine, Anirudh Rao
Chukwuma A Chukwu, Anirudh Rao, Department of Nephrology, Liverpool University Hospitals NHS Foundation Trust, Liverpool L7 8YE, Mersey Side, United Kingdom
Philip A Kalra, Department of Nephrology, Salford Royal Hospital, Northern Care Alliance NHS Foundation Trust, Manchester M6 8HD, Greater Manchester, United Kingdom
Philip A Kalra, Faculty of Biology, Medicine and Health, Department of Cardiovascular Medicine, University of Manchester, Manchester M13 9PL, Greater Manchester, United Kingdom
Marcus Lowe, Kay Poulton, Department of Population Health, Health Services Research and Primary Care, University of Manchester, Manchester M13 9PL, Greater Manchester, United Kingdom
Marcus Lowe, Kay Poulton, Transplantation Laboratory, Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester M13 9PL, Greater Manchester, United Kingdom
Titus Augustine, Department of Renal and Pancreatic Transplantation, Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester M13 9PL, Greater Manchester, United Kingdom
Titus Augustine, Department of Diabetes, Endocrinology and Gastroenterology, University of Manchester, Manchester M13 9PL, Greater Manchester, United Kingdom
Author contributions: Chukwu CA performed analysis and interpretation of data and drafted the initial manuscript; Chukwu CA, Lowe M, Poulton K, Augustine T, and Rao A contributed to acquisition of data; Chukwu CA, Kalra PA, Augustine T, and Rao A contributed to critical revision of manuscript for intellectual content; Chukwu CA, Augustine T, and Rao A initiated study concepts and design; Kalra PA and Augustine T provided administrative support and overall study supervision; all authors thoroughly reviewed and endorsed the final manuscript.
Institutional review board statement: This study was approved by and registered with the Northern Care Alliance Research and Innovation Department in the United Kingdom, No. S21HIP03.
Informed consent statement: This study was conducted using routinely collected clinical data that had been fully anonymised prior to analysis. As such, no identifiable patient information was used. The study was reviewed and approved by the appropriate institutional review board, which determined that written informed consent was not required in accordance with local regulations and ethical guidelines.
Conflict-of-interest statement: All authors declare no conflict of interest in publishing the manuscript.
STROBE statement: The authors have read the STROBE Statement – checklist of items, and the manuscript was prepared and revised according to the STROBE Statement – checklist of items.
Data sharing statement: The dataset supporting the findings of this study has been deposited in Mendeley Data and is publicly available at: 10.17632/3vdszzmz2n.1.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Chukwuma A Chukwu, PhD, Consultant, Department of Nephrology, Liverpool University Hospitals NHS Foundation Trust, Mount Vernon Street, Liverpool L7 8YE, Mersey Side, United Kingdom. chukwuma.chukwu@rlbuht.nhs.uk
Received: July 15, 2025
Revised: October 9, 2025
Accepted: December 9, 2025
Published online: March 18, 2026
Processing time: 184 Days and 7.4 Hours
Abstract
BACKGROUND

The use of induction immunosuppression agents has improved kidney transplant outcomes, but selecting the optimal agent remains a point of debate.

AIM

To compare the long-term outcomes of kidney transplant recipients receiving alemtuzumab vs basiliximab induction, focusing on graft function, acute rejection, infection, malignancy, post-transplant glomerulonephritis, and survival, using a propensity score matched cohort design.

METHODS

Kidney transplant recipients who received alemtuzumab or basiliximab induction from 2014 to 2019 across two nephrology centres in Northwest England were evaluated. Propensity score matching at a 1:1.5 ratio ensured comparability between cohorts. Baseline characteristics, immunosuppression regimens, and outcomes were analyzed. Linear, binary logistic and Cox proportional hazard regression models.

RESULTS

A total of 436 recipients were included, with a median follow-up of 5.2 years. The matched cohort (n = 262) had a mean age of 51.1 ± 13.5 years; 39% were female and 92% were white. There was no significant difference in the cumulative incidence of acute rejection [odds ratio (OR) = 2.10; 95%CI: 0.9-4.9; P = 0.110]. Compared with basiliximab, alemtuzumab was associated with lower estimated glomerular filtration rate at 12 months (-6.6 mL/minute/1.73 m2; 95%CI: -10.5 to -2.7; P < 0.001) and higher risks of cytomegalovirus viremia (OR = 3.2; 95%CI: 1.6-6.5; P < 0.001), BK viremia (OR = 2.4; 95%CI: 1.1-5.5; P = 0.02), post-transplant malignancy (OR = 6.2; 95%CI: 1.6-29.9; P = 0.013), and death-censored graft loss (hazard ratio = 3.6; 95%CI: 1.2-11.4; P = 0.03). No significant differences were observed in post-transplant glomerulonephritis or recipient mortality.

CONCLUSION

In this propensity score-matched analysis, alemtuzumab induction was associated with lower graft function at 12 months and higher risks of viral infection, post-transplant malignancy, and graft loss compared with basiliximab. These findings highlight the need for further studies to confirm the long-term safety and effectiveness of alemtuzumab in kidney transplantation.

Keywords: Kidney transplantation; Immunosuppression induction; Alemtuzumab; Basiliximab; Graft outcomes

Core Tip: This retrospective cohort study compared real-world outcomes of alemtuzumab and basiliximab induction in kidney transplant recipients from two tertiary centers in North-West England, one routinely using alemtuzumab and the other exclusively basiliximab. Using propensity score matching to reduce confounding, we evaluated graft function, graft and patient survival, acute rejection, infection, and other long-term complications. Alemtuzumab induction was found to be associated with lower estimated glomerular filtration rate, and higher risks of cytomegalovirus and BK viremia, post-transplant malignancy, and death-censored graft loss compared with basiliximab. These findings emphasize the need for individualized selection of induction therapy, balancing the potent immunosuppressive effects of alemtuzumab against its potential for adverse outcomes, and support tailored approaches based on recipient risk profile and center-specific experience.