Volume 24, Issue 5 pp. 701-708

Measurement of CD4+ T-cell function in predicting allograft rejection and recurrent hepatitis C after liver transplantation

Koji Hashimoto

Koji Hashimoto

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Charles Miller

Charles Miller

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Kenzo Hirose

Kenzo Hirose

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Teresa Diago

Teresa Diago

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Federico Aucejo

Federico Aucejo

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Cristiano Quintini

Cristiano Quintini

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Bijan Eghtesad

Bijan Eghtesad

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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Rebecca CoreyLisa Yerian

Lisa Yerian

Anatomic Pathology

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Rocio Lopez

Rocio Lopez

Quantitative Health Sciences

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Nizar Zein

Nizar Zein

Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH, USA

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John Fung

John Fung

Departments of Hepato-Pancreato-Biliary and Transplant Surgery

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First published: 28 December 2009
Citations: 33
Corresponding author: Charles Miller, MD, Department of Hepato-Pancreato-Biliary and Transplant Surgery, Digestive Disease Institute, Cleveland Clinic, 9500 Euclid Ave., Cleveland, OH 44195, USA.
Tel.: 216 445 2381; fax: 216 444 9375;
e-mail: [email protected]

Abstract

Hashimoto K, Miller C, Hirose K, Diago T, Aucejo F, Quintini C, Eghtesad B, Corey R, Yerian L, Lopez R, Zein N, Fung J. Measurement of CD4+ T-cell function in predicting allograft rejection and recurrent hepatitis C after liver transplantation.
Clin Transplant 2009 DOI: 10.1111/j.1399-0012.2009.01169.x
© 2009 John Wiley & Sons A/S.

Abstract: Recurrence of hepatitis C virus (HCV) can be difficult to distinguish from acute cellular rejection (ACR) following liver transplantation. The Cylex Immune Function Assay (ImmuKnow) provides objective measure of recipient’s immune function. The goal is to assess the ability of this assay to distinguish these similar conditions. A retrospective review was performed in 54 recipients with HCV. ImmuKnow assays were measured with allograft biopsies. Levels of adenosine triphosphate (ATP) release from CD4+ T cells (ng/mL) were compared with the following biopsy result classifications: 365 ± 130 with ACR (n = 11), 152 ± 100 with recurrent HCV (n = 26), 240 ± 71 with normal biopsies (n = 12), and 157 ± 130 with overlapping features of ACR and recurrent HCV (n = 5). Recipients with recurrent HCV had lower immune response than those with ACR (p < 0.0001).Using a cutoff level of 220, the sensitivity and specificity for distinguishing two conditions were 88.5% and 90.9%, respectively. When recipients with overlapping features had low immune response, three of four recipients’ subsequent biopsies showed recurrent HCV. In conclusion, the ImmuKnow assay can be a sensitive and specific additional test for distinguishing recurrent HCV from ACR and may be useful for predicting which recipients may be most vulnerable to recurrent HCV.

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