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05/10/2019 13:56

New findings on local inflammatory processes in the liver

Dr. Susanne Stöcker Presse, Informationen
Paul-Ehrlich-Institut - Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel

    The precise knowledge on organ-specific processes in inflammatory conditions is the basis of new ideas for approaches to targeted therapies with fewer undesirable effects. Researchers of the PEI have gained new findings in liver-specific inflammatory processes – in this context the receptor for interleukin-1ß is in the focus. The Journal Frontiers in Immunology reports on the research results in its online edition of 09.05.2019.

    Due to its very high complexity and its pro-inflammatory and anti-inflammatory messenger substances (cytokines), the immune system is not fully understood yet. Type I interferons form a major group of messenger substances that influence more than 300 genes, thus significantly contributing to the activity of the immune system. In previous experiments, Professor Dr Zoe Waibler, head of Section Product Testing of immunological biomedicines of Division ”Immunology” at the Paul-Ehrlich-Institut, and her colleagues found out how type-I-interferons can protect the liver. Mice in which type I interferons are unable to mediate their effects (type I interferon receptor (IFNAR) deficient mice) developed severe liver inflammation after the respective treatment, while those animals that had the IFNAR did not. This has been related to an imbalance of pro-inflammatory and anti-inflammatory cytokines of the interleukin-1 family.

    In their current study, the researchers have asked the question why in IFNAR-deficient mice, only the liver, but no other organs, e.g. the spleen are affected by this damage. To find out, they used poly(I:C), similarly to their preceding studies. Poly(I:C) is an artificial double-stranded RNA, which is able to activate the immune system in an unspecific manner, as is the case, e.g. in virus infections. The researchers were surprised to find that pro-inflammatory and anti-inflammatory cytokines in IFNAR-deficient mice showed an imbalance not only in the liver but also in other, intact organs. Other important parameters, too, did not differ when the liver and the spleen were studied in mice with or without IFNAR: Other messenger substances of the immune system were largely distributed evenly in damaged and intact organs. The same applied to important immune cells. Finally, the researchers discovered the difference: An important receptor is expressed (formed) in different ways in the organs: The receptor in question is the receptor for interleukin-1β, which is expressed in the liver but not in the spleen. Interleukin-1β is a cytokine with strong inflammatory properties. Thus, in the absence of type I interferon, interleukin-1βis expressed upon poly(I:C) treatment to damage the liver but not the spleen, where the receptor for interleukin-1β is missing. Findings on different distributions of important receptors in different organs provide a contribution to finding targeted therapies with fewer adverse effects.

    Original publication:

    Anzaghe M, Resch T, Schaser E, Kronhart S, Diez C, Niles MA, Korotkova E, Schülke S, Wolfheimer S, Kreuz D, Wingerter M, Bartolomé Rodríguez MM, Waibler Z (2019): Organ-specific expression of IL-1 receptor results in severe liver injury in type I interferon receptor deficient mice.
    Front Immunol May 9 [Epub ahead of print].

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    Criteria of this press release:
    Journalists, Scientists and scholars
    Biology, Medicine, Nutrition / healthcare / nursing
    transregional, national
    Research results, Scientific Publications

    Histology of IFNAR-deficient mice after treatment with RNA: Mice with the interleukin-1-receptor develop liver damage (left), while the liver of mice without this receptor remains intact (right).

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