Allospecific CD154+ T cells identify rejection-prone recipients after pediatric small-bowel transplantation

• Published in: Surgery Vol. 146; no. 2; pp. 166 - 173
• Main Authors: Ashokkumar, Chethan, PhD, Gupta, Ankit, MD, Sun, Qing, MS, Ningappa, Mylarappa B., PhD, Higgs, Brandon W., PhD, Mazariegos, George, MD, Fazzolare, Tamara, MPAS, Remaley, Lisa, MPAS, Soltys, Kyle, MD, Bond, Geoffrey, MD, Abu-Elmagd, Kareem, MD, PhD, Sindhi, Rakesh, MD
• Format: Journal Article
• Language: English
• Published: New York, NY Mosby, Inc 01.08.2009; Elsevier
• Subjects: Biological and medical sciences; CD40 Ligand - immunology; Child, Preschool; Female; General aspects; Graft Rejection - immunology; Humans; Immunologic Memory; Immunosuppressive Agents - administration & dosage; Intestine, Small - transplantation; Isoantigens - analysis; Lymphocyte Culture Test, Mixed; Male; Medical sciences; Surgery; T-Lymphocyte Subsets; T-Lymphocytes, Cytotoxic - immunology; T-Lymphocytes, Helper-Inducer - immunology; Tacrolimus - administration & dosage; Human; Graft(material); Pediatrics; Digestive system; Recipient; Transplantation; Small intestine; Medicine; Rejection; Treatment; Surgery; T-Lymphocyte; Graft; Child
• ISSN: 0039-6060; 1532-7361
• DOI: 10.1016/j.surg.2009.04.006

Background Up to 70% of children with small bowel transplantation (SBTx) experience acute cellular rejection (ACR). Allospecific CD154+ T cells predict liver ACR in children in a novel, 16-hour mixed leukocyte response (MLR) assay, but remain untested in SBTx. Methods The expression of CD154 was measured in 4 subsets—naive (N) and memory (M) CD154+ T-helper (Th) and T-cytotoxic (Tc) cells (ie, CD154+ ThN, CD154+ ThM, CD154+ TcN, and CD154+ TcM, respectively)—in the MLR of single blood samples obtained from 32 children with SBTx within 60 days of SBTx biopsy. Children showing ACR in these biopsies were termed Rejectors. The ratio of donor-induced to third-party–induced CD154+ T cells was called the immunoreactivity index (IR). We hypothesized that IR >1 denoted increased donor-specific alloreactivity and increased risk of rejection; in contrast, IR <1 implied decreased risk. CD154 expression was correlated with the expression of CTLA4, a negative T-cell costimulator that antagonizes and is inversely related to CD154 ( n = 18). Results Rejectors showed significantly greater numbers of donor-specific CD154+ T-cell subsets. Logistic regression analysis and leave-one-out cross validation followed by receiver operating characteristic analysis showed that, among the 4 subsets, IR ≥1.23 for CD154+ TcM identified Rejectors with a sensitivity and specificity of 93% and 88%. Also, a significant negative correlation was observed between CD154 expression and CTLA4 expression in allospecific Tc (Spearman's rho = –0.616, P = .006) but not in Th. Conclusion Allospecific CD154+ TcM identify rejection-prone children with SBTx.