Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients
The impact of h<b>uman leukocyte antigen</b> (HLA)-mismatching on the early appearance of subclinical inflammation (SCI) in low-immunological-risk kidney transplant (KT) recipients is undetermined. We aimed to assess whether HLA-mismatching (A-B-C-DR-DQ) is a risk factor for early SCI. A...
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Format: | Article |
Language: | English |
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MDPI AG
2021-04-01
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Series: | Journal of Clinical Medicine |
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Online Access: | https://www.mdpi.com/2077-0383/10/9/1934 |
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doaj-4459330796ec41ed885408ee8c729b52 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Domingo Hernández Teresa Vázquez Juana Alonso-Titos Myriam León Abelardo Caballero María Angeles Cobo Eugenia Sola Verónica López Pedro Ruiz-Esteban Josep María Cruzado Joana Sellarés Francesc Moreso Anna Manonelles Alberto Torio Mercedes Cabello Juan Delgado-Burgos Cristina Casas Elena Gutiérrez Cristina Jironda Julia Kanter Daniel Serón Armando Torres |
spellingShingle |
Domingo Hernández Teresa Vázquez Juana Alonso-Titos Myriam León Abelardo Caballero María Angeles Cobo Eugenia Sola Verónica López Pedro Ruiz-Esteban Josep María Cruzado Joana Sellarés Francesc Moreso Anna Manonelles Alberto Torio Mercedes Cabello Juan Delgado-Burgos Cristina Casas Elena Gutiérrez Cristina Jironda Julia Kanter Daniel Serón Armando Torres Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients Journal of Clinical Medicine kidney transplantation HLA compatibility subclinical inflammation Banff criteria low-immunological risk |
author_facet |
Domingo Hernández Teresa Vázquez Juana Alonso-Titos Myriam León Abelardo Caballero María Angeles Cobo Eugenia Sola Verónica López Pedro Ruiz-Esteban Josep María Cruzado Joana Sellarés Francesc Moreso Anna Manonelles Alberto Torio Mercedes Cabello Juan Delgado-Burgos Cristina Casas Elena Gutiérrez Cristina Jironda Julia Kanter Daniel Serón Armando Torres |
author_sort |
Domingo Hernández |
title |
Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients |
title_short |
Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients |
title_full |
Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients |
title_fullStr |
Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients |
title_full_unstemmed |
Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant Recipients |
title_sort |
impact of hla mismatching on early subclinical inflammation in low-immunological-risk kidney transplant recipients |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2021-04-01 |
description |
The impact of h<b>uman leukocyte antigen</b> (HLA)-mismatching on the early appearance of subclinical inflammation (SCI) in low-immunological-risk kidney transplant (KT) recipients is undetermined. We aimed to assess whether HLA-mismatching (A-B-C-DR-DQ) is a risk factor for early SCI. As part of a clinical trial (Clinicaltrials.gov, number NCT02284464), a total of 105 low-immunological-risk KT patients underwent a protocol biopsy on the third month post-KT. As a result, 54 presented SCI, showing a greater number of total HLA-mismatches (<i>p </i>= 0.008) and worse allograft function compared with the no inflammation group (48.5 ± 13.6 vs. 60 ± 23.4 mL/min; <i>p </i>= 0.003). Multiple logistic regression showed that the only risk factor associated with SCI was the total HLA-mismatch score (OR 1.32, 95%CI 1.06–1.64, <i>p </i>= 0.013) or class II HLA mismatching (OR 1.51; 95%CI 1.04–2.19, <i>p </i>= 0.032) after adjusting for confounder variables (recipient age, delayed graft function, transfusion prior KT, and tacrolimus levels). The ROC curve illustrated that the HLA mismatching of six antigens was the optimal value in terms of sensitivity and specificity for predicting the SCI. Finally, a significantly higher proportion of SCI was seen in patients with >6 vs. ≤6 HLA-mismatches (62.3 vs. 37.7%; <i>p </i>= 0.008). HLA compatibility is an independent risk factor associated with early SCI. Thus, transplant physicians should perhaps be more aware of HLA mismatching to reduce these early harmful lesions. |
topic |
kidney transplantation HLA compatibility subclinical inflammation Banff criteria low-immunological risk |
url |
https://www.mdpi.com/2077-0383/10/9/1934 |
work_keys_str_mv |
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doaj-4459330796ec41ed885408ee8c729b522021-04-29T23:08:11ZengMDPI AGJournal of Clinical Medicine2077-03832021-04-01101934193410.3390/jcm10091934Impact of HLA Mismatching on Early Subclinical Inflammation in Low-Immunological-Risk Kidney Transplant RecipientsDomingo Hernández0Teresa Vázquez1Juana Alonso-Titos2Myriam León3Abelardo Caballero4María Angeles Cobo5Eugenia Sola6Verónica López7Pedro Ruiz-Esteban8Josep María Cruzado9Joana Sellarés10Francesc Moreso11Anna Manonelles12Alberto Torio13Mercedes Cabello14Juan Delgado-Burgos15Cristina Casas16Elena Gutiérrez17Cristina Jironda18Julia Kanter19Daniel Serón20Armando Torres21Nephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainPathology Department, Hospital Regional Universitario de Malaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainImmunology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Malaga, SpainNephrology Department, Instituto de Tecnologías Biomédicas-Universidad La Laguna, Hospital Universitario de Canarias, REDinREN (RD16/0009/0031), E-38320 Tenerife, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Universitari de Bellvitge, University of Barcelona, IDIBELL, REDinREN (RD16/0009/0003), E-08907 Barcelona, SpainNephrology Department, Hospital Universitari Valld’Hebron, Universitat Autonoma, Barcelona, REDinREN (RD16/0009/0030), E-08035 Barcelona, SpainNephrology Department, Hospital Universitari Valld’Hebron, Universitat Autonoma, Barcelona, REDinREN (RD16/0009/0030), E-08035 Barcelona, SpainNephrology Department, Hospital Universitari de Bellvitge, University of Barcelona, IDIBELL, REDinREN (RD16/0009/0003), E-08907 Barcelona, SpainImmunology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Malaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Regional Universitario de Málaga, University of Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), REDinREN (RD16/0009/0006), E-29010 Málaga, SpainNephrology Department, Hospital Universitario Dr. Peset, E-46017 Valencia, SpainNephrology Department, Hospital Universitari Valld’Hebron, Universitat Autonoma, Barcelona, REDinREN (RD16/0009/0030), E-08035 Barcelona, SpainNephrology Department, Instituto de Tecnologías Biomédicas-Universidad La Laguna, Hospital Universitario de Canarias, REDinREN (RD16/0009/0031), E-38320 Tenerife, SpainThe impact of h<b>uman leukocyte antigen</b> (HLA)-mismatching on the early appearance of subclinical inflammation (SCI) in low-immunological-risk kidney transplant (KT) recipients is undetermined. We aimed to assess whether HLA-mismatching (A-B-C-DR-DQ) is a risk factor for early SCI. As part of a clinical trial (Clinicaltrials.gov, number NCT02284464), a total of 105 low-immunological-risk KT patients underwent a protocol biopsy on the third month post-KT. As a result, 54 presented SCI, showing a greater number of total HLA-mismatches (<i>p </i>= 0.008) and worse allograft function compared with the no inflammation group (48.5 ± 13.6 vs. 60 ± 23.4 mL/min; <i>p </i>= 0.003). Multiple logistic regression showed that the only risk factor associated with SCI was the total HLA-mismatch score (OR 1.32, 95%CI 1.06–1.64, <i>p </i>= 0.013) or class II HLA mismatching (OR 1.51; 95%CI 1.04–2.19, <i>p </i>= 0.032) after adjusting for confounder variables (recipient age, delayed graft function, transfusion prior KT, and tacrolimus levels). The ROC curve illustrated that the HLA mismatching of six antigens was the optimal value in terms of sensitivity and specificity for predicting the SCI. Finally, a significantly higher proportion of SCI was seen in patients with >6 vs. ≤6 HLA-mismatches (62.3 vs. 37.7%; <i>p </i>= 0.008). HLA compatibility is an independent risk factor associated with early SCI. Thus, transplant physicians should perhaps be more aware of HLA mismatching to reduce these early harmful lesions.https://www.mdpi.com/2077-0383/10/9/1934kidney transplantationHLA compatibilitysubclinical inflammationBanff criterialow-immunological risk |