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Complement Binding Anti-HLA Antibodies and the Survival of Kidney Transplantation.
Muñoz-Herrera, Claudia M; Gutiérrez-Bautista, Juan Francisco; López-Nevot, Miguel Ángel.
Afiliação
  • Muñoz-Herrera CM; Departamento de Bioquímica, Biología Molecular e Inmunología III, University of Granada, 18010 Granada, Spain.
  • Gutiérrez-Bautista JF; Programa de Doctorado en Biomedicina, University of Granada, 18010 Granada, Spain.
  • López-Nevot MÁ; Servicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, 18014 Granada, Spain.
J Clin Med ; 12(6)2023 Mar 17.
Article em En | MEDLINE | ID: mdl-36983335
ABSTRACT

BACKGROUND:

Antibody-mediated rejection (AMR) is one of the most important challenges in the context of renal transplantation, because the binding of de novo donor-specific antibodies (dnDSA) to the kidney graft triggers the activation of the complement, which in turn leads to loss of transplant. In this context, the objective of this study was to evaluate the association between complement-fixing dnDSA antibodies and graft loss as well as the possible association between non-complement-fixing antibodies and transplanted organ survival in kidney transplant recipients.

METHODS:

Our study included a cohort of 245 transplant patients over a 5-year period at Virgen de las Nieves University Hospital (HUVN) in Granada, Spain.

RESULTS:

dnDSA was observed in 26 patients. Of these patients, 17 had non-complement-fixing dnDSA and 9 had complement-fixing dnDSA.

CONCLUSIONS:

Our study demonstrated a significant association between the frequency of rejection and renal graft loss and the presence of C1q-binding dnDSA. Our results show the importance of the individualization of dnDSA, classifying them according to their ability to activate the complement, and suggest that the detection of complement-binding capacity by dnDSA could be used as a prognostic marker to predict AMR outcome and graft survival in kidney transplant patients who develop dnDSA.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article