Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease

Human inborn errors of IFN-γ underlie mycobacterial disease, due to insufficient IFN-γ production by lymphoid cells, impaired myeloid cell responses to this cytokine, or both. We report four patients from two unrelated kindreds with intermittent monocytosis and mycobacterial disease, including bacil...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 118; no. 15; pp. 1 - 12
Main Authors Le Voyer, Tom, Neehus, Anna-Lena, Yang, Rui, Ogishi, Masato, Rosain, Jérémie, Alroqi, Fayhan, Alshalan, Maha, Blumental, Sophie, Ali, Fatima Al, Khan, Taushif, Ata, Manar, Rozen, Laurence, Demulder, Anne, Bastard, Paul, Gruber, Conor, Roynard, Manon, Seeleuthener, Yoann, Rapaport, Franck, Bigio, Benedetta, Chrabieh, Maya, Sng, Danielle, Berteloot, Laureline, Boddaert, Nathalie, Rozenberg, Flore, Al-Muhsen, Saleh, Bertoli-Avella, Aida, Abel, Laurent, Bogunovic, Dusan, Marr, Nico, Mansouri, Davood, Mutairi, Fuad Al, Béziat, Vivien, Weil, Dominique, Mahdaviani, Seyed Alireza, Ferster, Alina, Zhang, Shen-Ying, Reversade, Bruno, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Bustamante, Jacinta
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 13.04.2021
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Summary:Human inborn errors of IFN-γ underlie mycobacterial disease, due to insufficient IFN-γ production by lymphoid cells, impaired myeloid cell responses to this cytokine, or both. We report four patients from two unrelated kindreds with intermittent monocytosis and mycobacterial disease, including bacillus Calmette–Guérin-osis and disseminated tuberculosis, and without any known inborn error of IFN-γ. The patients are homozygous for ZNFX1 variants (p.S959* and p.E1606Rfs*10) predicted to be loss of function (pLOF). There are no subjects homozygous for pLOF variants in public databases. ZNFX1 is a conserved and broadly expressed helicase, but its biology remains largely unknown. It is thought to act as a viral double-stranded RNA sensor in mice, but these patients do not suffer from severe viral illnesses. We analyze its subcellular localization upon overexpression in A549 and HeLa cell lines and upon stimulation of THP1 and fibroblastic cell lines. We find that this cytoplasmic protein can be recruited to or even induce stress granules. The endogenous ZNFX1 protein in cell lines of the patient homozygous for the p.E1606Rfs*10 variant is truncated, whereas ZNFX1 expression is abolished in cell lines from the patients with the p.S959* variant. Lymphocyte subsets are present at normal frequencies in these patients and produce IFN-γ normally. The hematopoietic and nonhematopoietic cells of the patients tested respond normally to IFN-γ. Our results indicate that human ZNFX1 is associated with stress granules and essential for both monocyte homeostasis and protective immunity to mycobacteria.
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1A.-L.N., R.Y., and M.O. contributed equally to this work.
Reviewers: M.A.B., McGill International TB Centre; and A.S.K., Strasbourg University Hospital.
3J.-L.C. and J.B. contributed equally to this work.
Contributed by Jean-Laurent Casanova, March 5, 2021 (sent for review February 11, 2021; reviewed by Marcel A. Behr and Anne Sophie Korganow)
Author contributions: T.L.V., J.-L.C., and J.B. designed research; T.L.V., A.-L.N., R.Y., J.R., M.O., M. Alshalan, F.A.A., T.K., M. Ata, C.G., D.B., N.M., F.A.M., V.B., and S.B.-D. performed research; M.R., M.C., S.-Y.Z., and S.B.-D. contributed new reagents/analytic tools; M. Alshalan, F.A.A., T.K., M. Ata, P.B., Y.S., F. Rapaport, B.B., L.B., N.B., L.A., N.M., F.A.M., D.W., and S.-Y.Z. analyzed data; T.L.V., J.-L.C., and J.B. wrote the paper; T.L.V., S.B.-D., and J.B. recorded the clinical data and created the figures; F.A., S.B., D.S., S.A.-M., A.B.-A., D.M., F.A.M., S.A.M., A.F., and B.R. provided samples and performed clinical diagnosis and follow-up of the kindreds; L.R. and A.D. recorded the clinical data; and F. Rozenberg performed viral serological analyses.
2F.A.M., V.B., D.W., S.A.M., A.F., S.-Y.Z., B.R., and S.B.-D. contributed equally to this work.
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.2102804118