IL-12 and IL-23—Close Relatives with Structural Homologies but Distinct Immunological Functions

Cytokines of the IL-12 family show structural similarities but have distinct functions in the immune system. Prominent members of this cytokine family are the pro-inflammatory cytokines IL-12 and IL-23. These two cytokines share cytokine subunits and receptor chains but have different functions in a...

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Published inCells (Basel, Switzerland) Vol. 9; no. 10; p. 2184
Main Authors Floss, Doreen M., Moll, Jens M., Scheller, Jürgen
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 28.09.2020
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Abstract Cytokines of the IL-12 family show structural similarities but have distinct functions in the immune system. Prominent members of this cytokine family are the pro-inflammatory cytokines IL-12 and IL-23. These two cytokines share cytokine subunits and receptor chains but have different functions in autoimmune diseases, cancer and infections. Accordingly, structural knowledge about receptor complex formation is essential for the development of new therapeutic strategies preventing and/or inhibiting cytokine:receptor interaction. In addition, intracellular signaling cascades can be targeted to inhibit cytokine-mediated effects. Single nucleotide polymorphisms can lead to alteration in the amino acid sequence and thereby influencing protein functions or protein–protein interactions. To understand the biology of IL-12 and IL-23 and to establish efficient targeting strategies structural knowledge about cytokines and respective receptors is crucial. A highly efficient therapy might be a combination of different drugs targeting extracellular cytokine:receptor assembly and intracellular signaling pathways.
AbstractList Cytokines of the IL-12 family show structural similarities but have distinct functions in the immune system. Prominent members of this cytokine family are the pro-inflammatory cytokines IL-12 and IL-23. These two cytokines share cytokine subunits and receptor chains but have different functions in autoimmune diseases, cancer and infections. Accordingly, structural knowledge about receptor complex formation is essential for the development of new therapeutic strategies preventing and/or inhibiting cytokine:receptor interaction. In addition, intracellular signaling cascades can be targeted to inhibit cytokine-mediated effects. Single nucleotide polymorphisms can lead to alteration in the amino acid sequence and thereby influencing protein functions or protein–protein interactions. To understand the biology of IL-12 and IL-23 and to establish efficient targeting strategies structural knowledge about cytokines and respective receptors is crucial. A highly efficient therapy might be a combination of different drugs targeting extracellular cytokine:receptor assembly and intracellular signaling pathways.
Audience Academic
Author Floss, Doreen M.
Scheller, Jürgen
Moll, Jens M.
AuthorAffiliation Institute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich-Heine-University, D-40225 Düsseldorf, Germany; jens.moll@uni-duesseldorf.de (J.M.M.); jscheller@uni-duesseldorf.de (J.S.)
AuthorAffiliation_xml – name: Institute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich-Heine-University, D-40225 Düsseldorf, Germany; jens.moll@uni-duesseldorf.de (J.M.M.); jscheller@uni-duesseldorf.de (J.S.)
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  givenname: Jürgen
  surname: Scheller
  fullname: Scheller, Jürgen
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Snippet Cytokines of the IL-12 family show structural similarities but have distinct functions in the immune system. Prominent members of this cytokine family are the...
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SubjectTerms Amino acid sequence
Autoimmune diseases
Chemical bonds
Clinical trials
Cytokines
Drug delivery
IL-12
IL-12 family cytokines
IL-23
Immune system
Immunosuppressive agents
Inflammation
Interleukin 12
Interleukin 23
Interleukins
Intracellular
Intracellular signalling
Mutation
Observations
Physiological aspects
Protein interaction
Quality control
Review
Signal transduction
signaling
Single-nucleotide polymorphism
Structure
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Title IL-12 and IL-23—Close Relatives with Structural Homologies but Distinct Immunological Functions
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https://pubmed.ncbi.nlm.nih.gov/PMC7600943
https://doaj.org/article/eaaf16bbf8c04eec906976fa69521f60
Volume 9
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