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Relationship Among Viremia/Viral Infection, Alloimmunity, and Nutritional Parameters in the First Year After Pediatric Kidney Transplantation
Author(s) -
Ettenger R.,
Chin H.,
Kesler K.,
Bridges N.,
Grimm P.,
Reed E. F.,
Sarwal M.,
Sibley R.,
Tsai E.,
Warshaw B.,
Kirk A. D.
Publication year - 2017
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/ajt.14169
Subject(s) - alloimmunity , viremia , medicine , transplantation , kidney transplantation , immunology , virology , human immunodeficiency virus (hiv)
The Immune Development in Pediatric Transplantation ( IMPACT ) study was conducted to evaluate relationships among alloimmunity, protective immunity, immune development, physical parameters, and clinical outcome in children undergoing kidney transplantation. We prospectively evaluated biopsy‐proven acute rejection ( BPAR ), de novo donor‐specific antibody ( dn DSA ) formation, viremia, viral infection, T cell immunophenotyping, and body mass index (BMI) /weight Z scores in the first year posttransplantation in 106 pediatric kidney transplant recipients. Outcomes were excellent with no deaths and 98% graft survival. Rejection and dn DSAs occurred in 24% and 22%, respectively. Pretransplant cytomegalovirus (CMV) and Epstein–Barr virus (EBV) serologies and subsequent viremia were unrelated to BPAR or dn DSA . Viremia occurred in 73% of children ( EBV , 34%; CMV , 23%; BMK viremia , 23%; and JC virus , 21%). Memory lymphocyte phenotype at baseline was not predictive of alloimmune complications. Patients who developed viral infection had lower weight (−2.1) (p = 0.028) and BMI (−1.2) (p = 0.048) Z scores at transplantation. The weight difference persisted to 12 months compared with patients without infection (p = 0.038). These data indicate that there is a high prevalence of viral disease after pediatric kidney transplantation, and underweight status at transplantation appears to be a risk factor for subsequent viral infection. The occurrence of viremia/viral infection is not associated with alloimmune events.