Abstract

Rodent models of rheumatoid arthritis (RA) have been used over decades to study the immunopathogenesis of the disease and to explore intervention strategies. Nevertheless, mouse models of RA reach their limit when it comes to testing of new therapeutic approaches such as cell-based therapies. Differences between the human and the murine immune system make it difficult to draw reliable conclusions about the success of immunotherapies. To overcome this issue, humanized mouse models have been established that mimic components of the human immune system in mice. Two main strategies have been pursued for humanization: the introduction of human transgenes such as human leukocyte antigen molecules or specific T cell receptors, and the generation of mouse/human chimera by transferring human cells or tissues into immunodeficient mice. Recently, both approaches have been combined to achieve more sophisticated humanized models of autoimmune diseases. This review discusses limitations of conventional mouse models of RA-like disease and provides a closer look into studies in humanized mice exploring their usefulness and necessity as preclinical models for testing of cell-based therapies in autoimmune diseases such as RA.

Highlights

  • Rheumatoid arthritis (RA) is a chronic inflammatory disorder which affects the synovial tissue of the joints, causing articular pain and disability [1]

  • While monocyte-derived dendritic cells (DCs) are used for clinical applications in humans [25], DCs obtained from bone marrow precursors are administered in mouse models [26, 27], which considerably affects the transferability of the results from mice to men

  • This review provides an overview of mouse models of RA-like disease and their limitations and discusses different humanization strategies for the generation of RA models, with focus on the use of humanized mice as tools for pre-clinical testing

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Summary

Introduction

Rheumatoid arthritis (RA) is a chronic inflammatory disorder which affects the synovial tissue of the joints, causing articular pain and disability [1]. Rosloniec and coworkers followed the second approach to establish Tg mice expressing chimeric HLA-DRB1∗0101 (DR1)/I-E or DR4/IE, which developed severe autoimmune arthritis following immunization with bovine or human CII, accompanied by strong DR1 and DR4-restricted T and B cell responses, respectively [13, 145].

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