Academic Journal

Urinary CD20 mRNA as a surrogate of CD20-positive cells infiltration during allograft dysfunction in renal transplant patients

التفاصيل البيبلوغرافية
العنوان: Urinary CD20 mRNA as a surrogate of CD20-positive cells infiltration during allograft dysfunction in renal transplant patients
المؤلفون: Ponciano, Viviane C. UNIFESP, Soares, Maria Fernanda Sanches UNIFESP, Naka, Erika L. UNIFESP, Arruda, Erika F. UNIFESP, Cenedeze, Marcos A. UNIFESP, Franco, Marcello F. UNIFESP, Pacheco-Silva, Alvaro UNIFESP, Camara, Niels O. S. UNIFESP
المساهمون: Universidade Federal de São Paulo (UNIFESP)
بيانات النشر: Elsevier B.V.
سنة النشر: 2009
المجموعة: Universidade Federal de São Paulo (UNIFESP): Repositório Institucional
مصطلحات موضوعية: B cells, Acute rejection, CD20, Renal transplant
الوصف: B lymphocyte infiltration in renal acute allograft rejection has been associated with steroid resistance and poor outcomes. We aimed to measure CD20 mRNA in urine of renal transplant patients with graft dysfunction and correlate with the histological diagnosis and immunohistochemical (IH) staining for CD20. A total of 48 urine samples were analyzed (21 with acute rejection, 10 with chronic allograft nephropathy, 11 with unspecific tubular lesions, 3 with acute pyelonephritis and 3 with polyomavirus nephropathy), Higher urinary CD20 levels associated with a positive IH staining for CD20 (>50 positive cells/HPF) in renal tissue (p = 0.04), with a sensitivity of 83.3% and a specificity of 51.6%. Within the acute rejection group, a positive staining for CD20 was not associated with graft loss, steroid resistance or lack of return to basal creatinine after treatment, but was associated with higher serum creatinine at 3 and 6 months, I and 2 years after the acute episode (p < 0.05). in conclusion, we showed that urinary levels of CD20 detected by RT-PCR had a high sensitivity for CD20+ staining in the corresponding renal tissue, but with a low specificity. Patients with clusters of CD20+ cells > 50/HPF had higher serum creatinine after 2 years of follow up. (C) 2008 Elsevier B.V. All rights reserved. ; Universidade Federal de São Paulo, Div Nephrol, Clin & Expt Immunol Lab, BR-04023900 São Paulo, Brazil ; Universidade Federal de São Paulo, Div Pathol, BR-04023900 São Paulo, Brazil ; Universidade Federal de São Paulo, Lab Transplant Immunobiol, BR-04023900 São Paulo, Brazil ; Universidade Federal de São Paulo, Div Nephrol, Clin & Expt Immunol Lab, BR-04023900 São Paulo, Brazil ; Universidade Federal de São Paulo, Div Pathol, BR-04023900 São Paulo, Brazil ; Universidade Federal de São Paulo, Lab Transplant Immunobiol, BR-04023900 São Paulo, Brazil ; Web of Science
نوع الوثيقة: article in journal/newspaper
وصف الملف: 663-667
اللغة: English
تدمد: 1567-5769
Relation: International Immunopharmacology; http://dx.doi.org/10.1016/j.intimp.2008.11.017; International Immunopharmacology. Amsterdam: Elsevier B.V., v. 9, n. 6, p. 663-667, 2009.; http://repositorio.unifesp.br/handle/11600/31565; WOS:000266568800004
DOI: 10.1016/j.intimp.2008.11.017
الاتاحة: http://repositorio.unifesp.br/handle/11600/31565
https://doi.org/10.1016/j.intimp.2008.11.017
Rights: Acesso restrito ; http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
رقم الانضمام: edsbas.D25740EA
قاعدة البيانات: BASE
الوصف
تدمد:15675769
DOI:10.1016/j.intimp.2008.11.017