4.8 Review

Dirty Fish Versus Squeaky Clean Mice: Dissecting Interspecies Differences Between Animal Models of Interferonopathy

Journal

FRONTIERS IN IMMUNOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2020.623650

Keywords

type I interferonopathy; Aicardi-Goutieres syndrome; autoimmune disease; RNASET2; zebrafish; mouse; white matter disorders; leukodystrophy

Categories

Funding

  1. MRC Discovery Medicine North (DiMeN) Doctoral Training Partnership [MR/N013840/1]
  2. New Investigator Grant from the MRC [MR/T03291X/1]
  3. Stroke Association [TSA LECT 2017/02]
  4. MRC [MR/T03291X/1] Funding Source: UKRI

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Autoimmune and autoinflammatory diseases are rare but devastating disorders, involving genetic and infectious factors. Researchers use animal models to explore pathological mechanisms and therapy development, uncovering differences between rodent and zebrafish models in the study of disease pathologies.
Autoimmune and autoinflammatory diseases are rare but often devastating disorders, underpinned by abnormal immune function. While some autoimmune disorders are thought to be triggered by a burden of infection throughout life, others are thought to be genetic in origin. Among these heritable disorders are the type I interferonopathies, including the rare Mendelian childhood-onset encephalitis Aicardi-Goutieres syndrome. Patients with Aicardi Goutieres syndrome are born with defects in enzymes responsible for nucleic acid metabolism and develop devastating white matter abnormalities resembling congenital cytomegalovirus brain infection. In some cases, common infections preceded the onset of the disease, suggesting immune stimulation as a potential trigger. Thus, the antiviral immune response has been actively studied in an attempt to provide clues on the pathological mechanisms and inform on the development of therapies. Animal models have been fundamental in deciphering biological mechanisms in human health and disease. Multiple rodent and zebrafish models are available to study type I interferonopathies, which have advanced our understanding of the human disease by identifying key pathological pathways and cellular drivers. However, striking differences in phenotype have also emerged between these vertebrate models, with zebrafish models recapitulating key features of the human neuropathology often lacking in rodents. In this review, we compare rodent and zebrafish models, and summarize how they have advanced our understanding of the pathological mechanisms in Aicardi Goutieres syndrome and similar disorders. We highlight recent discoveries on the impact of laboratory environments on immune stimulation and how this may inform the differences in pathological severity between mouse and zebrafish models of type I interferonopathies. Understanding how these differences arise will inform the improvement of animal disease modeling to accelerate progress in the development of therapies for these devastating childhood disorders.

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