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The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions
BACKGROUND: It is well known that ABO blood group system incompatible kidney transplantation (ABOi-KT) is an effective strategy for end-stage renal disease. The main barrier for ABOi-KT is how to keep host B cell activation and blood group antibody titer in low levels. Moreover, the mechanism of B c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732526/ https://www.ncbi.nlm.nih.gov/pubmed/29246114 http://dx.doi.org/10.1186/s12865-017-0233-9 |
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author | Cao, Jingsong Liu, Luogen Zhang, Yunsheng Xiao, Jianhua Wang, Yi |
author_facet | Cao, Jingsong Liu, Luogen Zhang, Yunsheng Xiao, Jianhua Wang, Yi |
author_sort | Cao, Jingsong |
collection | PubMed |
description | BACKGROUND: It is well known that ABO blood group system incompatible kidney transplantation (ABOi-KT) is an effective strategy for end-stage renal disease. The main barrier for ABOi-KT is how to keep host B cell activation and blood group antibody titer in low levels. Moreover, the mechanism of B cell activation induced by blood group antigen was unclear in ABOi-KT. RESULTS: In this study, HK2 cells were identified to express blood group B antigen when cocultured with lymphocytes of blood group A. Optical microscope observation demonstrated that HK2 cells in coculture group gradually decreased. Furthermore, flow cytometer assay identified that T cell phenotypes (CD3(+), CD3(+)CD4(+) and CD3(+)CD8(+)) had no significant change and B cell phenotypes (CD19(+) and CD138(+)) were all significantly enhanced (3.07 and 3.02 folds) at day 4. In addition, immunoturbidimetry analysis demonstrated that blood group B antibody was significantly increased to 2.35 fold at day 4, IgG was significantly increased to 3.60 and 2.81 folds at days 4 and 8 respectively, while IgM had no significant change at the measured time points. CONCLUSIONS: Taken together, B cells were activated and secreted blood group B antibody after treatment with HK2 expressing blood group B antigen. The results of this study maybe useful for further determination of the mechanism of B cell activation after ABO incompatible kidney endothelial cells stimulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12865-017-0233-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5732526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57325262017-12-21 The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions Cao, Jingsong Liu, Luogen Zhang, Yunsheng Xiao, Jianhua Wang, Yi BMC Immunol Research Article BACKGROUND: It is well known that ABO blood group system incompatible kidney transplantation (ABOi-KT) is an effective strategy for end-stage renal disease. The main barrier for ABOi-KT is how to keep host B cell activation and blood group antibody titer in low levels. Moreover, the mechanism of B cell activation induced by blood group antigen was unclear in ABOi-KT. RESULTS: In this study, HK2 cells were identified to express blood group B antigen when cocultured with lymphocytes of blood group A. Optical microscope observation demonstrated that HK2 cells in coculture group gradually decreased. Furthermore, flow cytometer assay identified that T cell phenotypes (CD3(+), CD3(+)CD4(+) and CD3(+)CD8(+)) had no significant change and B cell phenotypes (CD19(+) and CD138(+)) were all significantly enhanced (3.07 and 3.02 folds) at day 4. In addition, immunoturbidimetry analysis demonstrated that blood group B antibody was significantly increased to 2.35 fold at day 4, IgG was significantly increased to 3.60 and 2.81 folds at days 4 and 8 respectively, while IgM had no significant change at the measured time points. CONCLUSIONS: Taken together, B cells were activated and secreted blood group B antibody after treatment with HK2 expressing blood group B antigen. The results of this study maybe useful for further determination of the mechanism of B cell activation after ABO incompatible kidney endothelial cells stimulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12865-017-0233-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-16 /pmc/articles/PMC5732526/ /pubmed/29246114 http://dx.doi.org/10.1186/s12865-017-0233-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Cao, Jingsong Liu, Luogen Zhang, Yunsheng Xiao, Jianhua Wang, Yi The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions |
title | The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions |
title_full | The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions |
title_fullStr | The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions |
title_full_unstemmed | The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions |
title_short | The influence of HK2 blood group antigen on human B cell activation for ABOi-KT conditions |
title_sort | influence of hk2 blood group antigen on human b cell activation for aboi-kt conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732526/ https://www.ncbi.nlm.nih.gov/pubmed/29246114 http://dx.doi.org/10.1186/s12865-017-0233-9 |
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