Abstract

Fluorodeoxyglucose (FDG) uptake by alveolar echinococcosis (AE) liver lesions is a signal of their metabolic activity and of disease progression. In order to find a surrogate marker for this status, we investigated whether parameters of the peripheral and/or periparasitic immune responses were associated with metabolic activity in a prospective case-control study of 30 AE patients and 22 healthy controls. Levels of 18 cytokines and chemokines, representative of innate and adaptive immune responses, were assessed in plasma and peripheral cells of two groups of patients with (MAAE) and without (MIAE) metabolically active lesions, and in the liver of MAAE patients. Mixed cytokine profile was observed in the peripheral blood of AE patients, with a predominance of Th2, Th17 and Treg responses. Among the detected markers only plasma IL-5 and IL-23, more elevated in MAAE patients, were found discriminant. Discrimination between MAAE and MIAE patients obtained by using IL-23 was improved when IL-5 was used in combination. The combination of elevated levels of IL-5 and IL-23 is significantly associated with FDG uptake at PET scan. It offers a new tool for the follow-up of AE patients which could substitute to FDG-PET whenever non-available to assess disease progression.

Highlights

  • Human alveolar echinococcosis (AE) caused by the larval stage of Echinococcus multilocularis (E. multilocularis) is a public health threat because of its cancer-like progression

  • Overall proportion of Echinococcus multilocularis specific antigen positive was significantly higher in metabolically active alveolar echinococcosis (MAAE) patients than in metabolically inactive alveolar echinococcosis (MIAE) patients

  • No study had been performed to assess the relationship, if any, between the metabolically active status and peripheral parameters of the immune response that could be used as surrogate markers

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Summary

Introduction

Human alveolar echinococcosis (AE) caused by the larval stage of Echinococcus multilocularis (E. multilocularis) is a public health threat because of its cancer-like progression. Several studies have focused on this cross-talk and the possible role of dendritic cells, T helper (Th) cells and the cytokines they produce both in humans and experimental models[10,11] They have usually separately addressed peripheral or regional immune response; in addition, comparison between progression, stability or regression of lesions, whenever studied, was assessed on clinical grounds only[12,13,14]. Finding a surrogate marker of this metabolic activity is crucial for a proper care management strategy in any individual patient[8] For this purpose, and in order to analyze T cell and related cytokine immune response profile in peripheral blood mononuclear cells and plasma of both MAAE and MIAE patients, as well as in the hepatic lesions of MAAE patients, this study included 30 AE patients and 22 healthy controls prospectively

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