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Antibody‐mediated rejection in pediatric small bowel transplantation: Capillaritis is a major determinant of C4d positivity in intestinal transplant biopsies
Authors:Marion Rabant  Maud Racapé  Laetitia‐Marie Petit  Jean Luc Taupin  Olivier Aubert  Julie Bruneau  Patrick Barbet  Olivier Goulet  Christophe Chardot  Caroline Suberbielle  Florence Lacaille  Danielle Canioni  Jean‐Paul Duong Van Huyen
Affiliation:1. Pathology Department, H?pital Necker, Assistance Publique‐H?pitaux de Paris, Paris, France;2. INSERM U1151, H?pital Necker, Paris, France;3. Paris V Descartes University, Sorbonne‐Paris‐Cité, Paris, France;4. Paris Translational Research for Organ Transplant INSERM U 970, PARCC, HEGP, Paris, France;5. Pediatric Gastroenterology Department, H?pital Necker, Assistance Publique‐H?pitaux de Paris, Paris, France;6. Immunology and histocompatibility laboratory, Saint Louis Hospital, Paris, France;7. Pediatric Surgery Department, H?pital Necker, Assistance Publique‐H?pitaux de Paris, Paris, France
Abstract:The diagnostic criteria for antibody‐mediated rejection (ABMR) after small bowel transplantation (SBT) are not clearly defined, although the presence of donor‐specific antibodies (DSAs) has been reported to be deleterious for graft survival. We aimed to determine the incidence and prognostic value of DSAs and C4d in pediatric SBT and to identify the histopathologic features associated with C4d positivity. We studied all intestinal biopsies (IBx) obtained in the first year posttransplantation (N = 345) in a prospective cohort of 23 children. DSAs and their capacity to fix C1q were identified by using Luminex technology. Eighteen patients (78%) had DSAs, and 9 had the capacity to fix C1q. Seventy‐eight IBx (22.6%) were C4d positive. The independent determinants of C4d positivity were capillaritis grades 2 and 3 (odds ratio [OR] 4.02, P = .047 and OR 5.17, P = .003, respectively), mucosal erosion/ulceration (OR 2.8, P = .019), lamina propria inflammation grades 1 and 2/3 (OR 1.95, P = .043 and OR 3.1, P = .016, respectively), and chorion edema (OR 2.16, P = .028). Complement‐fixing DSAs and repeated C4d‐positive IBx were associated with poor outcome (P = .021 and P = .001, respectively). Our results support that capillaritis should be considered as a feature of ABMR in SBT and identify C1q‐fixing DSAs and repeated C4d positivity as potential markers of poor outcome.
Keywords:biopsy  classification systems  clinical research/practice  intestinal (allograft) function/dysfunction  intestine/multivisceral transplantation  pathology/histopathology  rejection: antibody‐mediated (ABMR)
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