Abstract

KL-6 is an antigen produced mainly by damaged type II pneumocytes that is involved in interstitial lung disease. Chronic lung allograft dysfunction (CLAD) after lung transplantation (LT) is a major concern for LT clinicians, especially in patients with restrictive allograft syndrome (RAS). We investigated KL-6 levels in serum and bronchoalveolar lavage fluid (BALF) as a potential biomarker of the RAS phenotype. Levels of KL-6 in serum and BALF were measured in 73 bilateral LT recipients, and patients were categorized into 4 groups: stable (ST), infection (LTI), bronchiolitis obliterans syndrome (BOS), and RAS. We also studied a healthy cohort to determine reference values for serum KL-6. The highest levels of KL-6 were found in the serum of patients with RAS (918 [487.8–1638] U/mL). No differences were found for levels of KL-6 in BALF. Using a cut-off value of 465 U/mL serum KL-6 levels was able to differentiate RAS patients from BOS patients with a sensitivity of 100% and a specificity of 75%. Furthermore, higher serum KL-6 levels were associated with a decline in Forced Vital Capacity (FVC) at 6 months after sample collection. Therefore, KL-6 in serum may well be a potential biomarker for differentiating between the BOS and RAS phenotypes of CLAD in LT recipients.

Highlights

  • Chronic lung allograft dysfunction (CLAD) is one of the main challenges facing lung transplantation (LT) clinicians which continues to affect long-term survival [1]

  • 18 patients with LT were in stable condition (ST), 24 were infected (LTI), 20 had bronchiolitis obliterans syndrome (BOS), and 11 had restrictive allograft syndrome (RAS)

  • LT patients diagnosed with active infection (LTI) consisted of bacterial isolation in 14 patients (58%), fungal isolation in 3 patients, and coinfection of bacterial and viral infection in 7 patients

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Summary

Introduction

Chronic lung allograft dysfunction (CLAD) is one of the main challenges facing lung transplantation (LT) clinicians which continues to affect long-term survival [1]. A robust description for the term CLAD including its definition, etiology, phenotypes, pathology, treatment and outcome, has been recently published by the Pulmonary Council of the International Society for Heart and Lung Transplantation (ISHLT) [2]. In the ISHLT report CLAD was defined as a substantial and persistent decline ( 20%) in measured forced expiratory volume in 1. Serum KL-6 level for detecting restrictive allograft syndrome after lung transplantation

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