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Uric acid increases cellular and humoral alloimmunity in primary human peripheral blood mononuclear cells

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Autor
Eleftheriadis T., Pissas G., Sounidaki M., Antoniadi G., Antoniadis N., Liakopoulos V., Stefanidis I.
Fecha
2018
Language
en
DOI
10.1111/nep.13069
Materia
alloantibody
uric acid
alloantibody
uric acid
adult
alloimmunity
antibody dependent cellular cytotoxicity
antibody production
Article
cell proliferation
cell survival
cellular immunity
controlled study
human
human cell
humoral immunity
male
mixed lymphocyte reaction
peripheral blood mononuclear cell
priority journal
autoimmunity
cell culture
cellular immunity
drug effect
humoral immunity
immunology
lymphocyte activation
metabolism
mixed lymphocyte culture
mononuclear cell
Adult
Autoimmunity
Cell Proliferation
Cells, Cultured
Humans
Immunity, Cellular
Immunity, Humoral
Isoantibodies
Leukocytes, Mononuclear
Lymphocyte Activation
Lymphocyte Culture Test, Mixed
Uric Acid
Blackwell Publishing
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Resumen
Aim: Hyperuricaemia is common among kidney transplant recipients and has been associated with worse graft outcome. Since episodes of acute cellular rejection and chronic humoral rejection contribute to decreased graft survival, in this study the effect of uric acid on cellular and humoral alloimmunity was evaluated. Methods: Cellular alloimmunity was assessed by cell proliferation in two-way mixed lymphocyte reaction (MLR) with human peripheral blood mononuclear cells (PBMC). For assessing humoral alloimmunity we developed a method in which humoral alloimmunity was induced in one-way MLR. Then the de novo production of alloantibodies was measured with an antibody-mediated complement-dependent cytotoxicity assay, in which supernatants from the above MRLs were used against resting PBMC similar to the stimulator cells of the above MLRs. Results: Uric acid at a concentration above its crystallization threshold increased cellular proliferation in two-way MLRs. Supernatants from one-way MLRs performed in the presence of uric acid were more cytotoxic against PBMC from individuals that had conferred the stimulator cells for the above MLRs. Conclusions: Uric acid increases both cellular and humoral alloimmunity in human PBMC. These results offer a possible pathogenetic mechanism for the observed relation between hyperuricaemia and worse kidney allograft survival. © 2017 Asian Pacific Society of Nephrology
URI
http://hdl.handle.net/11615/71354
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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