Abstract

The interplay between thyroid hormone action and the immune system has been established in physiological and pathological settings. However, their connection is complex and still not completely understood. The thyroid hormones (THs), 3,3′,5,5′ tetraiodo-L-thyroxine (T4) and 3,3′,5-triiodo-L-thyronine (T3) play essential roles in both the innate and adaptive immune responses. Despite much research having been carried out on this topic, the available data are sometimes difficult to interpret or even contradictory. Innate immune cells act as the first line of defense, mainly involving granulocytes and natural killer cells. In turn, antigen presenting cells, macrophages and dendritic cells capture, process and present antigens (self and foreign) to naïve T lymphocytes in secondary lymphoid tissues for the development of adaptive immunity. Here, we review the cellular and molecular mechanisms involved in T4 and T3 effects on innate immune cells. An overview of the state-of-the-art of TH transport across the target cell membrane, TH metabolism inside these cells, and the genomic and non-genomic mechanisms involved in the action of THs in the different innate immune cell subsets is included. The present knowledge of TH effects as well as the thyroid status on innate immunity helps to understand the complex adaptive responses achieved with profound implications in immunopathology, which include inflammation, cancer and autoimmunity, at the crossroads of the immune and endocrine systems.

Highlights

  • Growing evidence compiled over recent decades has revealed a bidirectional crosstalk between thyroid hormones (THs) and the immune system

  • The role of THs in the initiation of adaptive immunity remained uncertain for many years, with Mooij et al providing the earliest clues that THs and other iodinated derivatives, mainly T3, favored the maturation of human peripheral blood monocytes into functional dendritic cells (DCs) [92]

  • T3 increased the ability of human DCs to upregulate the proliferative response and secretion of IL-12 by peripheral blood mononuclear cells, similar to our findings in mice splenocytes co-cultured with T3-stimulated DCs [93]

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Summary

Introduction

Growing evidence compiled over recent decades has revealed a bidirectional crosstalk between thyroid hormones (THs) and the immune system. The role of THs in the initiation of adaptive immunity remained uncertain for many years, with Mooij et al providing the earliest clues that THs and other iodinated derivatives, mainly T3, favored the maturation of human peripheral blood monocytes into functional DCs [92].

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