https://orcid.org/0000-0001-5874-8845
Figures
Abstract
Background
There is extensive literature with comparisons between Anti-Thymocyte Globulin (ATG) and Basiliximab (BSX) as induction therapy in kidney transplant recipients. The purpose of our benchmarking study was to describe the consequences in terms of practices in 6 transplantation centers of a French prospective cohort.
Methods
We included adult patients who received a first or second kidney graft between 2013 and 2019 (n = 4157). We used logistic regressions to identify characteristics associated with the use of ATG or BSX.
Results
Use of ATG between the centers ranged from 41% to 75%. We observed different factors associated with the treatment decision. Compared to a first transplant, performing a second graft was the only factor significantly associated with the choice of ATG in all centers. The AUC ranged from 0.67 to 0.91, indicating that the centers seemed to define their own rules. As a result, for patients with the same low immunological risk, the probability of receiving ATG varied from 7% to 36%. We stratified the analyses according to two periods, from 2013 to 2015 and from 2016 to 2019. A similar heterogeneity was observed, and in some cases ATG indications between the centers were inverted.
Citation: Boucquemont J, Foucher Y, Masset C, Legendre C, Scemla A, Buron F, et al. (2020) Induction therapy in kidney transplant recipients: Description of the practices according to the calendar period from the French multicentric DIVAT cohort. PLoS ONE 15(10): e0240929. https://doi.org/10.1371/journal.pone.0240929
Editor: Frank JMF Dor, Imperial College Healthcare NHS Trust, UNITED KINGDOM
Received: July 9, 2020; Accepted: October 6, 2020; Published: October 22, 2020
Copyright: © 2020 Boucquemont et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: The authors received no specific funding for this work.
Competing interests: Outside of the submitted work, Y. Foucher reported personal fees from Biogen and Sanofi-Genzyme; C. Legendre is a member of the advisory board for CSL Behring and Hansa Medical; E. Morelon reported personal fees from Astellas and Novartis; A. Sicard is membered of advisory Board for Novartis; M. Giral is membered of advisory board for Chiesi and reported personal fees from Astellas, Novartis and Sandoz. The DIVAT cohort is partially sponsored by Roche, Novartis, Chiesi, Astellas and Sanofi laboratories. This does not alter our adherence to PLOS ONE policies on sharing data and materials. All authors of this manuscript have no relevant conflicts of interest to disclose for this study.
Introduction
The two main induction therapies used in kidney transplantation are anti-thymocyte globulin (ATG) and Basiliximab (BSX). ATG (Thymoglobulin® or Grafalon Fresenius®) is a polyclonal antibody primarily targeting T-cells but also other immune and non-immune cells [1, 2]. BSX (Simulect®) is a chimeric mouse-human monoclonal antibody that targets the α chain (CD25) of the T-cell IL-2 receptor.
Whilst ATG is known to provide better outcomes for high immunological risk patients [3–5], so far there is no evidence of an effect on graft survival [6, 7]. ATG can also be used to avoid steroid use and to delay the use of calcineurin inhibitors (CNI) without increasing rejection rates [8, 9]. It may also prevent delayed graft function (DGF), which is known to increase allograft immunogenicity and the risk of acute rejection [10–13]. ATG is therefore recommended after a long cold ischemia time (CIT) or for recipients receiving an expanded criteria donor graft (ECD, including donors after cardiac death), two possible risk factors of DGF.
ATG-related adverse events are also well-documented. It can induce cytokine release syndrome and serum sickness [2, 14]. Whilst it is also associated with higher rates of CMV infection [11, 15], other issues such as the risk of cancer or diabetes remain uncertain [11, 16–18]. Consequently, for patients at low risk of acute rejection or DGF, BSX, or even no induction therapy, might be more relevant [19].
The theoretical risk-benefit related to the choice between ATG and BSX appears to be based on recommendations from moderate quality evidence and guidelines based on studies mostly conducted before 2013 [19–21]. These recommendations which are based on the efficacy in preventing graft rejection and DGF must also be counterbalanced against the risk of serious adverse events, as described above. For instance, even though elderly recipients are more likely to receive marginal grafts, this population is also more sensitive to ATG-related side effects due to the reduction in immune system function that occurs with age. Few studies have investigated the factors associated with the choice of treatment in transplantation [22–24]. In general, these show that variations in the prescribed treatment was more reflective of center pratices than patients’ profiles. However, these studies were conducted using US registry data and/or pharmacy fill records for patients transplanted before 2015. Furthermore, only the Dharnidharka et al study [22] investigated induction therapy, whilst the two others focused on immunosuppression regimens. To our knowledge, no recent study of a European cohort exists. The purpose of our benchmarking study was to describe the current prescription patterns for induction therapy using ATG compared to BSX in each transplantation center in a French prospective cohort, and to determine whether these have changed over time.
Materials and methods
Patients
We extracted data from the French DIVAT cohort (www.divat.fr) of kidney transplant recipients in Lyon, Montpellier, Nancy, Nantes, Nice, and Paris Necker. Data from the DIVAT cohort is available free of charge to academic researchers after a request to its scientific council. The procedure is explained at this address: http://www.divat.fr/access-to-data. The “Comité National Informatique et Liberté” approved the study (CNIL number for the cohort: #891735) and written informed consent was obtained from the participants.
We randomly assigned a letter for each center (A to F). In this study, we focused on first and second kidney transplantations performed between January 2013 and December 2019 in adults, receiving a transplant from a living donor or deceased donor and having received either ATG or BSX as induction therapy. Note that we had no data for 2018 and 2019 for center D, and no data for 2017 to 2019 for center F because of a delay in the data collection. We excluded donors after cardiac death and multiple organ transplants. We also excluded grafts with missing data for anti-HLA class I or II immunization before transplantation due to their importance in the choice of induction therapy. This represented between 0.6% and 10.0% of the patients in each center. The characteristics of included and excluded recipients are described in S1 Table.
Available data
We considered the following parameters: recipient age, recipient gender, recipient body mass index (BMI), diabetes, cardiovascular and cancer history, recipient cytomegalovirus (CMV) serostatus, CIT, renal replacement therapy, donor age, donor gender, donor type, donor CMV status, donor and recipient Epstein-Barr virus (EBV) serostatus, graft year, transplantation rank, last donor creatinemia level, number of HLA incompatibilities (A+B+DR), and anti-HLA class I and II immunization. For this last parameter, all centers used Luminex technology for anti-HLA antibody determination, except center D where lymphocytotoxic antibody determination was used for half of the transplantations. Flow cytometry MFI thresholds used to define positivity were: 2000 in center A, 1000 in centers C and D, and 500 in centers B, E, and F.
Statistical analyses
We used two-sided ANOVA, Student’s t-tests, Chi-square, or Fisher statistics for the cohort description. We fitted six logistic regressions to describe the determinants of the induction in each center. We considered all of the significant parameters differentially expressed between the ATG and the BSX groups (p<0.20). To obtain the same set of determinants for each center, we progressively removed the non-significant parameters for all centers (p>0.05). For each resulting model, we estimated the receiver operating characteristic (ROC) curves and the corresponding areas under the curve (AUC). The confidence intervals were obtained by non-parametric bootstrapping (1000 iterations). To investigate potential recent changes in characteristics associated with the choice of induction therapy, we stratified the analyses on two periods: from 2013 to 2015 and from 2016 to 2019. All analyses were performed using R version 3.6.
Results
Cohort description
As shown in Table 1, 2195 of the 4157 included kidney transplant recipients (52.8%) were treated by ATG, and this ranged from 41% to 75% between the centers. One can note that the immunization profile of patients also varied between centers. The proportion of pre-transplantation anti-HLA immunized patients was higher in center E (class I: 81.9%, class II: 82.9%) but lower in center B (class I: 19.0%, class II: 20.8%) and center F (class I: 22.6%, class II: 21.3%).
Table 2 presents the patient characteristics according to induction therapy in the whole cohort. Fig 1 and S2 to S7 Tables shows the data for each center. In the whole cohort, we observed that women more likely received ATG (40.1%) than BSX (30.9%). Also, ATG was prescribed more often for patients with pre-transplantation anti-HLA class I (57.4%) or II (54.9%) and re-transplantations (23.2%) compared to BSX (37.0%, 35.8%, and 4.5%, respectively). Patients with obesity or cardiovascular history before transplantation received more ATG than BSX, as were patients who received a graft from a marginal donor or with prolonged CIT. We also observed that patients receiving a preemptive transplant received more BSX induction (20.5%) than ATG (14.4%).
Decision of induction therapy
We aimed to more explicitly describe the decision of induction therapy. We did not consider several subgroups in the models’ estimations because of the corresponding quasi-systematic ATG decision: second kidney transplants in all centers except E, recipients with detectable anti-HLA class I immunization in center B, and transplantations from donors with a last creatinemia higher than 132.6 μmol/L in centers C and D.
We retained fifteen factors significantly associated with the induction prescription in at least one center: recipient age, gender, BMI, cardiovascular history, cancer history, recipient CMV status, pre-transplantation anti-HLA immunization against class I and II, renal replacement therapy, donor type, donor CMV status, year and rank of transplantation, last donor creatinemia, and CIT. We did not retain the EBV serostatus because too few seronegative recipients received a transplant from a seropositive donor.
Fig 2 shows the prescription decision process. An Odds-Ratio (OR) greater than 1 reflects increased ATG use. Favoring ATG as induction therapy was a homogeneous practice in re-transplanted patients and recipients with anti-HLA class I or class II immunization. In contrast, for the other predictive characteristics, we observed heterogeneities between centers. For instance, we observed significant differences between the different time-frames for the different centers; center A prescribed more ATG over time, while center B prescribed more BSX over time. From 2016 to 2017, centers C and F prescribed more BSX compared to 2013–2015. We observed the opposite trend for center D. Finally, no tendency to change was observed for the center E.
n = 484 for center A (only first transplant and transplants performed from 2013 to 2017), n = 604 for B (only first transplant and non-detectable anti-HLA Class I), n = 577 for C (only first transplant and last donor creatinemia < 132.6 μmol/L), n = 276 for D (only first transplant and last donor creatinemia < 132.6 μmol/L), n = 1045 for E, and n = 271 for F (only first transplant).
The AUC values ranged from 0.67 (CI95% from 0.64 to 0.71) to 0.91 (CI95% from 0.89 to 0.93). The higher the AUC value, the more that decision was predictable, i.e., the center protocol was standardized. Despite the wide variability in prescribing ATG between centers, these results illustrate that the centers seem to define their own (randomless) rules.
Fig 2 also reports the OR according to the timeframe (2013–2015 and 2016–2019). For these analyses, note that logistic regressions were conducted only for the hemodialyzed patients in center B for the period 2016–2019, and only for patients with a last donor creatininemia lower than 132.6 μmol/L for center D during the period from 2013 to 2015, ATG being used systematically in these populations. These analyses were not conducted for center F due to the small number of grafts in 2016. Independent of the timeframe, transplantation of a second graft was associated with greater ATG use compared to a first transplant. For the other characteristics, as in the main analysis, we observed heterogeneities between centers in each period. For example, recipient age was not associated with the choice of induction therapy in centers A and E, regardless of the timeframe. For centers B and C, older patients received more ATG during the period from 2013 to 2015 compared to 2016–2019. Finally, BSX was prescribed more for older patients in center D from 2013 to 2015 whereas ATG was higher from 2016 to 2019.
Standardized results to improve inter-center comparisons
We previously reported that ATG center-specific prevalence ranged from 41% to 75%. This range may be partially explained by the differences in the patient and transplantation characteristics between centers. By using the previous center-specific predictive models, we computed the expected (standardized) ATG prevalence in each center in the counterfactual world where all centers had patients with characteristics like the overall cohort (first column, Table 1). These standardized prevalence values were 58%, 71%, 74%, 57%, 34% and 48% for centers A to F, respectively.
We also computed the expected probability of receiving ATG in each center for two illustrative recipients by using the previous center-specific predictive models. The first recipient was a 35-year-old male, with a BMI < 30 kg/m2, without cardiovascular or cancer history, negative for CMV, without anti-HLA class I or II immunization, who received a first transplant after hemodialysis from a deceased donor, negative for CMV, with a last creatinemia < 132.6 μmol/L and a CIT equal to 28 hours. His expected probability of receiving ATG was 36.6%, 5.5%, 48.2%, 26.3%, 17.5% and 21.7% from centers A to F, respectively. For a similar patient with anti-HLA class I immunization before transplantation, the probabilities were 59.1%, 100.0%, 58.2%, 41.4%, 27.6%, and 32.5% from centers A to F, respectively.
Discussion
In this study, we describe for the first time the choice between ATG and BSX and its evolution as induction therapy in a multicentric French cohort of kidney transplant recipients. Approximately half of the patients received ATG, and we noted that there was considerable heterogeneity between centers (ranging from 41% to 75%). We also found that the factors associated with this decision were highly variable between centers, and we quantified this variabilty. Whilst it was not systematic, all centers tended to respect the international guidelines and preferred ATG induction therapy for all re-transplanted patients or almost all immunological high-risk patients with anti-HLA class I or class II immunization [20, 21, 25]. Considering the overall picture, most situations known to be associated with a high risk of delayed graft function are more frequently managed with ATG. Nevertheless, with the exception of anti-HLA immunization, we found that patient and transplantation characteristics associated with the decision to use ATG was highly variable between centers. More specifically, this did not appear to be guided by standardized rules but seemed to depend more on center-specific practices than on evidence-based results, as was shown for US transplant centers [22].
This raises the question of whether the current guidelines relating to the definition of the immunological risk of patients should be updated, given that these guidelines were drafted in an era before the current sensitive methods of anti-HLA antibody detection, i.e., Luminex assay (that is used in 95% of patients in our cohort). Moreover, monitoring of additional epitope mismatches, associated with increased allograft rejection risk [26], will also need to be included shortly [27, 28]. Overall, new data from emerging technologies that provide a better understanding of the pathophysiological processes must be incorporated to precisely define the pre-transplant risk of rejection and, therefore, the necessity for induction therapy by T-cell depletion.
Our results, obtained from analysis of a contempory European cohort, are in accordance with older studies conducted in the US [22–24]. This illustrates that despite efforts to standardize practices in the past, these remain heterogeneous. For instance, three of the French centers we studied did not change their medical decision making practices regarding the patient age. In contrast, two other centers changed their age-related ATG administration practices, but in opposite directions.
Clinicians need strong recommendations for prescribing induction therapy, particularly for low immunological risk patients, to avoid arbitrary decisions of the medical staff [20]. Whilst improved evidence based medicine may in general be supported by the weight of the literature, it is crucial to carefully filter and re-assess data using meta-analysis stratified by patient profiles.
Besides the lack of standard rules for induction decision-making, it was nevertheless interesting to observe that several centers referred to specific protocols that are highly standardized (AUC > 0.85 for two centers). Moreover, the specific center protocol is all the more possible in France because the social security system reimburses induction treatment on the basis of their authorization for use and not on the basis of a cost system.
It would have been interesting to assess the long-term results of such practices of induction therapy, but such a study is beyond our objectives. Our aim was not to find the best therapeutic option for patients but to underline the variability of practices between centers.
As usual in observational studies, our study presents several limitations. First, we excluded 260 grafts due to missing anti-HLA class I or II data. We observed more missing data for grafts performed in-between 2016 and 2017 and for re-transplantation. Second, because of the absence of systematic collection practices, the history of DSA was not considered in our analyses. Third, there were different thresholds between centers regarding the definition of positive anti-HLA class I and II, which can partially explain the differences in ATG prescription. However, we reported that standardized ATG prevalence values varied from 34% to 74%, supporting the fact that immunization, and patient profiles more generally, did not seem to explain practice heterogeneity. Note also that we did not have the details of the commercial kits used to detect anti-HLA immunization. Fourth, we were not able to account for research protocols that imposed the choice of induction therapy, as we did not collect this information in our database. Finally, we did not consider the ATG dose, which is also not collected. Recent pilot studies have reported the potential benefit of reduced ATG duration and dosage with good tolerance [29, 30]. Whilst this may have influenced the induction strategy in some centers, to date, a randomized trial to compare different dosage strategies has not been conducted.
In conclusion, our study quantified the persistant high variability of current practices in the choice of induction therapy, except for patients with high immunological risk. Our results call for more consensus, clinical research with more persuasive evidence, and meta-analysis stratified by patient profiles, especially for kidney transplant recipients with low immunological risk.
Supporting information
S1 Table. Comparison of the included versus excluded grafts because of missing data on anti-HLA class I or anti-HLA class II.
https://doi.org/10.1371/journal.pone.0240929.s001
(DOCX)
S2 Table. Characteristics at transplantation according to the induction therapy in center A.
https://doi.org/10.1371/journal.pone.0240929.s002
(DOCX)
S3 Table. Characteristics at transplantation according to the induction therapy in center B.
https://doi.org/10.1371/journal.pone.0240929.s003
(DOCX)
S4 Table. Characteristics at transplantation according to the induction therapy in center C.
https://doi.org/10.1371/journal.pone.0240929.s004
(DOCX)
S5 Table. Characteristics at transplantation according to the induction therapy in center D.
https://doi.org/10.1371/journal.pone.0240929.s005
(DOCX)
S6 Table. Characteristics at transplantation according to the induction therapy in center E.
https://doi.org/10.1371/journal.pone.0240929.s006
(DOCX)
S7 Table. Characteristics at transplantation according to the induction therapy in center F.
https://doi.org/10.1371/journal.pone.0240929.s007
(DOCX)
Acknowledgments
The authors would like to thank the members of the DIVAT^ consortium for their involvement in the study (lead author: Magali Giral, magali.giral@chu-nantes.fr), the physicians who helped recruit patients, and all patients who participated in this study. We also thank the clinical research associates who participated in the data collection. Data were collected from the French DIVAT multicentric prospective cohort of kidney and pancreatic transplant recipients (www.divat.fr, N° CNIL 914184). The analysis and interpretation of these data are the responsibility of the authors.
Données Informatisées et VAlidées en Transplantation, DIVAT Cohort Collaborators (Medical Doctors, Surgeons, HLA Biologists). Nantes: Gilles Blancho, Julien Branchereau, Diego Cantarovich, Agnès Chapelet, Jacques Dantal, Clément Deltombe, Lucile Figueres, Claire Garandeau, Magali Giral, Caroline Gourraud-Vercel, Maryvonne Hourmant, Georges Karam, Clarisse Kerleau, Aurélie Meurette, Simon Ville, Christine Kandell, Anne Moreau, Karine Renaudin, Anne Cesbron, Florent Delbos, Alexandre Walencik, Anne Devis; Paris-Necker: Lucile Amrouche, Dany Anglicheau, Olivier Aubert, Lynda Bererhi, Christophe Legendre, Alexandre Loupy, Frank Martinez, Rébecca Sberro-Soussan, Anne Scemla, Claire Tinel, Julien Zuber; Nancy: Pascal Eschwege, Luc Frimat, Sophie Girerd, Jacques Hubert, Marc Ladriere, Emmanuelle Laurain, Louis Leblanc, Pierre Lecoanet, Jean-Louis Lemelle; Lyon E. Hérriot: Lionel Badet, Maria Brunet, Fanny Buron, Rémi Cahen, Sameh Daoud, Coralie Fournie, Arnaud Grégoire, Alice Koenig, Charlène Lévi, Emmanuel Morelon, Claire Pouteil-Noble, Thomas Rimmelé, Olivier Thaunat; Montpellier: Sylvie Delmas, Georges Mourad, Moglie Le Quintrec, Jean-Emmanuel Serre; Nice: Laeticia Albano, Antoine Sicard.
References
- 1. Mourad G, Morelon E, Noël C, Glotz D, Lebranchu Y. The role of Thymoglobulin induction in kidney transplantation: an update. Clin Transpl 2012;26:E450–464. https://doi.org/10.1111/ctr.12021.
- 2. Thiyagarajan UM, Ponnuswamy A, Bagul A. Thymoglobulin and Its Use in Renal Transplantation: A Review. AJN 2013;37:586–601. https://doi.org/10.1159/000351643.
- 3. Noel C, Abramowicz D, Durand D, Mourad G, Lang P, Kessler M, et al. Daclizumab versus antithymocyte globulin in high-immunological-risk renal transplant recipients. J Am Soc Nephrol 2009;20:1385–92. pmid:19470677
- 4. Brennan DC, Daller JA, Lake KD, Cibrik D, Del Castillo D. Rabbit Antithymocyte Globulin versus Basiliximab in Renal Transplantation. N Engl J Med 2006;355:1967–77. pmid:17093248
- 5. Webster AC, Ruster LP, McGee R, Matheson SL, Higgins GY, Willis NS, et al. Interleukin 2 receptor antagonists for kidney transplant recipients. Cochrane Database Syst Rev 2010;(1):CD003897. pmid:20091551
- 6. Hellemans R, Hazzan M, Durand D, Mourad G, Lang P, Kessler M, et al. Daclizumab Versus Rabbit Antithymocyte Globulin in High-Risk Renal Transplants: Five-Year Follow-up of a Randomized Study. Am J Transplant 2015;15:1923–32. pmid:25707875
- 7. Lentine KL, Schnitzler MA, Xiao H, Brennan DC. Long-term safety and efficacy of antithymocyte globulin induction: use of integrated national registry data to achieve ten-year follow-up of 10–10 Study participants. Trials 2015;16:365. pmid:26285695
- 8. Cantarovich D, Rostaing L, Kamar N, Ducloux D, Saint-Hillier Y, Mourad G, et al. Early corticosteroid avoidance in kidney transplant recipients receiving ATG-F induction: 5-year actual results of a prospective and randomized study. Am J Transpl 2014;14:2556–64. https://doi.org/10.1111/ajt.12866.
- 9. Sureshkumar KK, Thai NL, Hussain SM, Ko TY, Marcus RJ. Influence of induction modality on the outcome of deceased donor kidney transplant recipients discharged on steroid-free maintenance immunosuppression. Transplantation 2012;93:799–805. pmid:22290269
- 10. Chapal M, Le Borgne F, Legendre C, Kreis H, Mourad G, Garrigue V, et al. A useful scoring system for the prediction and management of delayed graft function following kidney transplantation from cadaveric donors. Kidney Int 2014;86:1130–9. pmid:24897036
- 11. Hill P, Cross NB, Barnett ANR, Palmer SC, Webster AC. Polyclonal and monoclonal antibodies for induction therapy in kidney transplant recipients. Cochrane Database Syst Rev 2017;1:CD004759. pmid:28073178
- 12. Ulrich F, Niedzwiecki S, Pascher A, Kohler S, Weiss S, Fikatas P, et al. Long-term outcome of ATG vs. Basiliximab induction. Eur J Clin Invest 2011;41:971–8. pmid:21382021
- 13. Sollinger H, Kaplan B, Pescovitz MD, Philosophe B, Roza A, Brayman K, et al. Basiliximab versus antithymocyte globulin for prevention of acute renal allograft rejection. Transplantation 2001;72:1915–9. pmid:11773888
- 14. Couvrat-Desvergnes G, Salama A, Le Berre L, Evanno G, Viklicky O, Hruba P, et al. Rabbit antithymocyte globulin-induced serum sickness disease and human kidney graft survival. J Clin Invest 2015;125:4655–65. pmid:26551683
- 15. Clesca P, Dirlando M, Park S-I, García R, Ferraz E, Pinheiro-Machado PG, et al. Thymoglobulin and rate of infectious complications after transplantation. Transpl Proc 2007;39:463–4. https://doi.org/10.1016/j.transproceed.2007.01.024.
- 16. Cherikh WS, Kauffman HM, McBride MA, Maghirang J, Swinnen LJ, Hanto DW. Association of the type of induction immunosuppression with posttransplant lymphoproliferative disorder, graft survival, and patient survival after primary kidney transplantation. Transplantation 2003;76:1289–93. pmid:14627905
- 17. Lim WH, Turner RM, Chapman JR, Ma MKM, Webster AC, Craig JC, et al. Acute rejection, T-cell-depleting antibodies, and cancer after transplantation. Transplantation 2014;97:817–25. pmid:24521777
- 18. Hertig A, Zuckermann A. Rabbit antithymocyte globulin induction and risk of post-transplant lymphoproliferative disease in adult and pediatric solid organ transplantation: An update. Transpl Immunol 2015;32:179–87. pmid:25936966
- 19. Hellemans R, Bosmans J-L, Abramowicz D. Induction Therapy for Kidney Transplant Recipients: Do We Still Need Anti-IL2 Receptor Monoclonal Antibodies? Am J Transpl 2017;17:22–7. https://doi.org/10.1111/ajt.13884.
- 20. Baker RJ, Mark PB, Patel RK, Stevens KK, Palmer N. Renal association clinical practice guideline in post-operative care in the kidney transplant recipient. BMC Nephrol 2017;18:174. pmid:28571571
- 21. Kidney Disease: Improving Global Outcomes (KDIGO) Transplant Work Group. KDIGO clinical practice guideline for the care of kidney transplant recipients. Am J Transpl 2009;9 Suppl 3:S1–155. https://doi.org/10.1111/j.1600-6143.2009.02834.x.
- 22. Dharnidharka VR, Naik AS, Axelrod DA, Schnitzler MA, Zhang Z, Bae S, et al. Center practice drives variation in choice of US kidney transplant induction therapy: a retrospective analysis of contemporary practice. Transpl Int 2018;31:198–211. pmid:28987015
- 23. Nazzal M, Lentine KL, Naik AS, Ouseph R, Schnitzler MA, Zhang Z, et al. Center-driven and Clinically Driven Variation in US Liver Transplant Maintenance Immunosuppression Therapy: A National Practice Patterns Analysis. Transplant Direct 2018;4:e364. pmid:30046654
- 24. Axelrod DA, Naik AS, Schnitzler MA, Segev DL, Dharnidharka VR, Brennan DC, et al. National Variation in Use of Immunosuppression for Kidney Transplantation: A Call for Evidence-Based Regimen Selection. Am J Transpl 2016;16:2453–62. https://doi.org/10.1111/ajt.13758.
- 25. Pratschke J, Dragun D, Hauser IA, Horn S, Mueller TF, Schemmer P, et al. Immunological risk assessment: The key to individualized immunosuppression after kidney transplantation. Transplant Rev 2016;30:77–84. https://doi.org/10.1016/j.trre.2016.02.002.
- 26. Sypek M, Kausman J, Holt S, Hughes P. HLA Epitope Matching in Kidney Transplantation: An Overview for the General Nephrologist. Am J Kidney Dis 2018;71:720–31. pmid:29246419
- 27. Tambur AR. HLA-Epitope Matching or Eplet Risk Stratification: The Devil Is in the Details. Front Immunol 2018;9:Article 2010. pmid:30233594
- 28. Lim WH, Wong G, Heidt S, Claas FHJ. Novel aspects of epitope matching and practical application in kidney transplantation. Kidney Int 2018;93:314–24. pmid:29061333
- 29. Grafals M, Smith B, Murakami N, Trabucco A, Hamill K, Marangos E, et al. Immunophenotyping and efficacy of low dose ATG in non-sensitized kidney recipients undergoing early steroid withdrawal: a randomized pilot study. PloS One 2014;9:e104408. pmid:25111080
- 30. Patel HV, Kute VB, Vanikar AV, Shah PR, Gumber MR, Engineer DP, et al. Low-dose rabbit anti-thymoglobin globulin versus basiliximab for induction therapy in kidney transplantation. Saudi J Kidney Transpl 2014;25:819–22.