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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...

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Detalles Bibliográficos
Autores principales: Cao, Jingsong, Liu, Luogen, Zhang, Yunsheng, Xiao, Jianhua, Wang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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
Descripción
Sumario: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.