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Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria

Human inherited disorders of interferon-gamma (IFN-γ) immunity underlie severe mycobacterial diseases. We report X-linked recessive MCTS1 deficiency in men with mycobacterial disease from kindreds of different ancestries (from China, Finland, Iran, and Saudi Arabia). Complete deficiency of this tran...

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Main Authors: Bohlen, Jonathan (Author) , Zhou, Qinhua (Author) , Philippot, Quentin (Author) , Ogishi, Masato (Author) , Rinchai, Darawan (Author) , Nieminen, Tea (Author) , Seyedpour, Simin (Author) , Parvaneh, Nima (Author) , Rezaei, Nima (Author) , Yazdanpanah, Niloufar (Author) , Momenilandi, Mana (Author) , Conil, Clément (Author) , Neehus, Anna-Lena (Author) , Schmidt, Carltin (Author) , Arango-Franco, Carlos A. (Author) , Voyer, Tom Le (Author) , Khan, Taushif (Author) , Yang, Rui (Author) , Puchan, Julia (Author) , Erazo, Lucia (Author) , Roiuk, Mykola (Author) , Vatovec, Taja (Author) , Janda, Zarah (Author) , Bagarić, Ivan (Author) , Materna, Marie (Author) , Gervais, Adrian (Author) , Liang, Hailun (Author) , Rosain, Jérémie (Author) , Peel, Jessica N (Author) , Seeleuthner, Yoann (Author) , Han, Ji Eun (Author) , L’Honneur, Anne-Sophie (Author) , Moncada-Vélez, Marcela (Author) , Martin-Fernandez, Marta (Author) , Horesh, Michael E. (Author) , Kochetkova, Tatiana (Author) , Schmidt, Monika (Author) , AlShehri, Mohammed A. (Author) , Salo, Eeva (Author) , Saxen, Harri (Author) , ElGhazali, Gehad (Author) , Yatim, Ahmad (Author) , Soudée, Camille (Author) , Sallusto, Federica (Author) , Ensser, Armin (Author) , Marr, Nico (Author) , Zhang, Peng (Author) , Bogunovic, Dusan (Author) , Cobat, Aurélie (Author) , Shahrooei, Mohammad (Author) , Béziat, Vivien (Author) , Abel, Laurent (Author) , Wang, Xiaochuan (Author) , Boisson-Dupuis, Stéphanie (Author) , Teleman, Aurelio A. (Author) , Bustamante, Jacinta (Author) , Zhang, Qian (Author) , Casanova, Jean-Laurent (Author)
Format: Article (Journal)
Language:English
Published: 9 November 2023
In: Cell
Year: 2023, Volume: 186, Issue: 23, Pages: 5114-5134
ISSN:1097-4172
DOI:10.1016/j.cell.2023.09.024
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1016/j.cell.2023.09.024
Verlag, kostenfrei, Volltext: https://www.sciencedirect.com/science/article/pii/S0092867423010784
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Author Notes:Jonathan Bohlen, Qinhua Zhou, Quentin Philippot, Masato Ogishi, Darawan Rinchai, Tea Nieminen, Simin Seyedpour, Nima Parvaneh, Nima Rezaei, Niloufar Yazdanpanah, Mana Momenilandi, Clément Conil, Anna-Lena Neehus, Carltin Schmidt, Carlos A. Arango-Franco, Tom Le Voyer, Taushif Khan, Rui Yang, Julia Puchan, Lucia Erazo, Mykola Roiuk, Taja Vatovec, Zarah Janda, Ivan Bagarić, Marie Materna, Adrian Gervais, Hailun Li, Jérémie Rosain, Jessica N Peel, Yoann Seeleuthner, Ji Eun Han, Anne-Sophie L’Honneur, Marcela Moncada-Vélez, Marta Martin-Fernandez, Michael E. Horesh, Tatiana Kochetkov, Monika Schmidt, Mohammed A. AlShehri, Eeva Salo, Harri Saxen, Gehad ElGhazali, Ahmad Yatim, Camille Soudée, Federica Sallusto, Armin Ensser, Nico Marr, Peng Zhang, Dusan Bogunovic, Aurélie Cobat, Mohammad Shahrooei, Vivien Béziat, Laurent Abel, Xiaochuan Wang, Stéphanie Boisson-Dupuis, Aurelio A. Teleman, Jacinta Bustamante, Qian Zhang, and Jean-Laurent Casanova
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Summary:Human inherited disorders of interferon-gamma (IFN-γ) immunity underlie severe mycobacterial diseases. We report X-linked recessive MCTS1 deficiency in men with mycobacterial disease from kindreds of different ancestries (from China, Finland, Iran, and Saudi Arabia). Complete deficiency of this translation re-initiation factor impairs the translation of a subset of proteins, including the kinase JAK2 in all cell types tested, including T lymphocytes and phagocytes. JAK2 expression is sufficiently low to impair cellular responses to interleukin-23 (IL-23) and partially IL-12, but not other JAK2-dependent cytokines. Defective responses to IL-23 preferentially impair the production of IFN-γ by innate-like adaptive mucosal-associated invariant T cells (MAIT) and γδ T lymphocytes upon mycobacterial challenge. Surprisingly, the lack of MCTS1-dependent translation re-initiation and ribosome recycling seems to be otherwise physiologically redundant in these patients. These findings suggest that X-linked recessive human MCTS1 deficiency underlies isolated mycobacterial disease by impairing JAK2 translation in innate-like adaptive T lymphocytes, thereby impairing the IL-23-dependent induction of IFN-γ.
Item Description:Online verfügbar: 23. Oktober 2023
Gesehen am 09.02.2024
Physical Description:Online Resource
ISSN:1097-4172
DOI:10.1016/j.cell.2023.09.024

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