Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant
Authors:
- Stéphanie Boisson-DupuisSBStéphanie Boisson-Dupuis
- Noe Ramirez-AlejoNRNoe Ramirez-Alejo
- Zhi LiZLZhi Li
- Etienne PatinEPEtienne Patin
- Gaspard KernerGKGaspard Kerner
- Che Kang LimCLChe Kang Lim
- Dimitry N. KrementsovDKDimitry N. Krementsov
- Cindy S. MaCMCindy S. Ma
- Qian ZhangQZQian Zhang
- Janet MarkleJMJanet Markle
Top Cited Papers
- 14 December 2018
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science Immunology
- Vol. 3 (30)
Abstract
Inherited IL-12Rβ1 and TYK2 deficiencies impair both IL-12– and IL-23–dependent IFN-γ immunity and are rare monogenic causes of tuberculosis, each found in less than 1/600,000 individuals. We show that homozygosity for the common TYK2 P1104A allele, which is found in about 1/600 Europeans and between 1/1000 and 1/10,000 individuals in regions other than East Asia, is more frequent in a cohort of patients with tuberculosis from endemic areas than in ethnicity-adjusted controls (P = 8.37 × 10−8; odds ratio, 89.31; 95% CI, 14.7 to 1725). Moreover, the frequency of P1104A in Europeans has decreased, from about 9% to 4.2%, over the past 4000 years, consistent with purging of this variant by endemic tuberculosis. Surprisingly, we also show that TYK2 P1104A impairs cellular responses to IL-23, but not to IFN-α, IL-10, or even IL-12, which, like IL-23, induces IFN-γ via activation of TYK2 and JAK2. Moreover, TYK2 P1104A is properly docked on cytokine receptors and can be phosphorylated by the proximal JAK, but lacks catalytic activity. Last, we show that the catalytic activity of TYK2 is essential for IL-23, but not IL-12, responses in cells expressing wild-type JAK2. In contrast, the catalytic activity of JAK2 is redundant for both IL-12 and IL-23 responses, because the catalytically inactive P1057A JAK2, which is also docked and phosphorylated, rescues signaling in cells expressing wild-type TYK2. In conclusion, homozygosity for the catalytically inactive P1104A missense variant of TYK2 selectively disrupts the induction of IFN-γ by IL-23 and is a common monogenic etiology of tuberculosis.Keywords
Funding Information
- National Institutes of Health (R01AI089970)
- National Institutes of Health (R37AI095983)
- National Institutes of Health (U01AI088685)
- National Institutes of Health (U19AI111143)
- National Institutes of Health (UL1TR001866)
- Agence Nationale de la Recherche (ANR-10-IAHU-01)
- Agence Nationale de la Recherche (ANR-14-CE14-0007-01)
- Agence Nationale de la Recherche (ANR-10-LABX-62-IBEID)
- European Research Council (ERC-2010-AdG-268777)
- Canadian Institutes of Health Research (GPG-102170)
- National Health and Medical Research Council (1113904)
- National Health and Medical Research Council (1042925)
- Stony Wold-Herbert Fund
- Secretaría de Ciencia, Humanidades, Tecnología e Innovación (264011)
- Damon Runyon Cancer Research Foundation (PST-03-15)
- GENMSMD (ANR-16-CE17-0005-01)
- Support of Clinical Research (SRV2017)
- NSW Department of Health
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