Literature DB >> 19651178

Soluble total human leukocyte antigen class I and human leukocyte antigen-G molecules in kidney and kidney/pancreas transplantation.

Vera Rebmann1, Diana Bartsch, Andreas Wunsch, Petra Möllenbeck, Thomas Golda, Richard Viebahn, Hans Grosse-Wilde.   

Abstract

The expression of human leukocyte antigen (HLA)-G, a nonclassical HLA class I molecule, and its soluble forms (sHLA-G) are found to improve graft acceptance. In this study we investigated whether sHLA-G is the most biologically relevant molecule among all types of soluble HLA class I molecules for graft acceptance. We addressed this question in kidney-transplanted (n = 32) and kidney/pancreas-transplanted patients (n = 29). To this end we analyzed the levels of total soluble HLA class I (sHLA-I) in comparison to sHLA-G in 488 plasma samples procured before and serial after transplantation by specific enzyme-linked immunoabsorbent assay. Samples from 126 healthy individuals served as controls. Pretransplantation sHLA-I levels were significantly increased in patients (p < 0.001), whereas sHLA-G levels were in the range of those of healthy controls. Importantly, pretransplantation sHLA-I and sHLA-G levels did not differ between the two groups. Patients with biopsy-proven rejection (n = 15) revealed significantly lower sHLA-G levels before transplantation (mean +/- standard error of the mean, 12.9 +/- 1.8 vs. 20.1 +/- 1.9, p = 0.013) and after transplantation (p = 0.006, two-way analysis of variance) than patients without rejection (n = 46). In contrast, sHLA-I was slightly increased after but not before transplantation in patients with rejection (p < 0.05, two-way analysis of variance). Nonparametric determination analysis showed that pretransplantation levels of sHLA-G < 11.5 ng/ml (sensitivity, 60%; specificity, 80.4%) were related to rejection. Regarding antibody status, retransplantation, number of HLA mismatches, recipient age, and recipient body mass index, multivariate analysis showed that sHLA-G but not sHLA-I is an independent risk factor for graft rejection. Thus high levels of sHLA-G but not of sHLA-I seem to contribute to better graft acceptance after kidney or kidney/pancreas transplantation.

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Year:  2009        PMID: 19651178     DOI: 10.1016/j.humimm.2009.07.016

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


  13 in total

1.  Frequency of HLA-G exon 8 polymorphisms and kidney allograft outcome in Iranian population.

Authors:  Mahdokht H Aghdaie; Negar Azarpira; Kurosh Kazemi; Bita Geramizadeh; Masumeh Darai; Seid Ali Malekhoseini
Journal:  Mol Biol Rep       Date:  2010-11-24       Impact factor: 2.316

2.  Circulating and renal expression of HLA-G prevented chronic renal allograft dysfunction in Japanese recipients.

Authors:  Yuki Okushi; Kazuaki Okino; Kiyotaka Mukai; Yuki Matsui; Norifumi Hayashi; Keiji Fujimoto; Hiroki Adachi; Hideki Yamaya; Hitoshi Yokoyama
Journal:  Clin Exp Nephrol       Date:  2017-03-31       Impact factor: 2.801

3.  Identification of a novel HLA-G+ regulatory population in blood: expansion after allogeneic transplantation and de novo HLA-G expression at graft-versus-host disease sites.

Authors:  Ioanna Lazana; Anastasia Zoudiari; Dimitra Kokkinou; Maria Themeli; Maria Liga; Helen Papadaki; Dionysios Papachristou; Alexandros Spyridonidis
Journal:  Haematologica       Date:  2012-03-14       Impact factor: 9.941

4.  Role and expression of non-classical human leukocyte antigen-G in renal transplanted allografts.

Authors:  Sho Kumano; Yuki Okushi; Keiji Fujimoto; Hiroki Adachi; Kengo Furuichi; Hitoshi Yokoyama
Journal:  Clin Exp Nephrol       Date:  2021-01-04       Impact factor: 2.801

Review 5.  HLA-G in organ transplantation: towards clinical applications.

Authors:  Frederic Deschaseaux; Diego Delgado; Vito Pistoia; Massimo Giuliani; Fabio Morandi; Antoine Durrbach
Journal:  Cell Mol Life Sci       Date:  2010-11-20       Impact factor: 9.261

Review 6.  Biological Characteristics of HLA-G and Its Role in Solid Organ Transplantation.

Authors:  Siqi Liu; Nicolaas A Bos; Erik A M Verschuuren; Debbie van Baarle; Johanna Westra
Journal:  Front Immunol       Date:  2022-06-13       Impact factor: 8.786

7.  The plasma levels of soluble HLA-G molecules correlate directly with CD34+ cell concentration and HLA-G 14bp insertion/insertion polymorphism in cord blood donors.

Authors:  Cristina Capittini; Paola Bergamaschi; Sara Sachetto; Mariarosa Truglio; Monica Viola; Andrea Marchesi; Valeria Genovese; Bina Romano; Marco Guarene; Rossella Poma; Miryam Martinetti; Carmine Tinelli; Laura Salvaneschi
Journal:  Blood Transfus       Date:  2013-01-23       Impact factor: 3.443

Review 8.  Implications of the polymorphism of HLA-G on its function, regulation, evolution and disease association.

Authors:  Eduardo A Donadi; Erick C Castelli; Antonio Arnaiz-Villena; Michel Roger; Diego Rey; Philippe Moreau
Journal:  Cell Mol Life Sci       Date:  2010-11-24       Impact factor: 9.261

9.  The Mechanisms of Human Renal Epithelial Cell Modulation of Autologous Dendritic Cell Phenotype and Function.

Authors:  Sandeep Sampangi; Andrew J Kassianos; Xiangju Wang; Kenneth W Beagley; Travis Klein; Sadia Afrin; Helen Healy; Ray Wilkinson
Journal:  PLoS One       Date:  2015-07-31       Impact factor: 3.240

10.  HLA-G polymorphism (rs16375) and acute rejection in liver transplant recipients.

Authors:  Negar Azarpira; Mahdokht H Aghdaie; Kurosh Kazemi; Bita Geramizadeh; Masumeh Darai
Journal:  Dis Markers       Date:  2014-01-23       Impact factor: 3.434

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