PuSH - Publikationsserver des Helmholtz Zentrums München

Export: TXT Text RIS Endnote (RIS) BIB BibTeX
Capitani, M.* ; Al-Shaibi, A.A.* ; Pandey, S.* ; Gartner, L.* ; Taylor, H.A.* ; Hubrack, S.Z.* ; Agrebi, N.* ; Al-Mohannadi, M.J.* ; Al Kaabi, S.* ; Vogl, T.* ; Roth, J.* ; Kotlarz, D.M. ; Klein, C.* ; Charles, A.K.* ; Vijayakumar, V.* ; Karim, M.Y.* ; George, B.* ; Travis, S.P.* ; Elawad, M.* ; Lo, B.* ; Uhlig, H.H.*

Biallelic TLR4 deficiency in humans.

J. Allergy Clin. Immunol. 151, 783-790.e5 (2023)
Verlagsversion Postprint DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
BACKGROUND: Toll-like receptors (TLRs) mediate functions for host defense and inflammatory responses. TLR4 recognizes LPS, a component of gram-negative bacteria as well as host-derived endogenous ligands such as S100A8 and S100A9 proteins. OBJECTIVE: We sought to report phenotype and cellular function of individuals with complete TLR4 deficiency. METHODS: We performed genome sequencing and investigated exome and genome sequencing databases. Cellular responses were studied on primary monocytes, macrophages, and neutrophils, as well as cell lines using flow cytometry, reporter, and cytokine assays. RESULTS: We identified 2 individuals in a family of Qatari origin carrying a homozygous stop codon variant p.Q188X in TLR4 presenting with a variable phenotype (asymptomatic and inflammatory bowel disease consistent with severe perianal Crohn disease). A third individual with homozygous p.Y794X was identified in a population database. In contrast to hypomorphic polymorphisms p.D299G and p.T399I, the variants p.Q188X and p.Y794X completely abrogated LPS-induced cytokine responses whereas TLR2 response was normal. TLR4 deficiency causes a neutrophil CD62L shedding defect, whereas antimicrobial activity toward intracellular Salmonella was intact. CONCLUSIONS: Biallelic TLR4 deficiency in humans causes an inborn error of immunity in responding to LPS. This complements the spectrum of known primary immunodeficiencies, in particular myeloid differentiation primary response 88 (MYD88) or the IL-1 receptor-associated kinase 4 (IRAK4) deficiency that are downstream of TLR4 and TLR2 signaling.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Altmetric
14.200
0.000
2
Tags
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern

Zusatzinfos bearbeiten
Eigene Tags bearbeiten
Privat
Eigene Anmerkung bearbeiten
Privat
Auf Publikationslisten für
Homepage nicht anzeigen
Als besondere Publikation
markieren
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Inflammatory Bowel Disease ; Primary Immunodeficiency; Evolutionary Conservation; Protein; Recognition; Signals
Sprache englisch
Veröffentlichungsjahr 2023
Prepublished im Jahr 2022
HGF-Berichtsjahr 2022
ISSN (print) / ISBN 0091-6749
e-ISSN 1097-6825
Zeitschrift The journal of allergy and clinical immunology
Quellenangaben Band: 151, Heft: 3, Seiten: 783-790.e5 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam [u.a.]
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Translational Genomics (ITG)
POF Topic(s) 30205 - Bioengineering and Digital Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-506700-001
Förderungen
National Institute for Health Research (NIHR)
Biomedical Research Centre (BRC)
Sidra Medicine Internal Research Fund (IRF)
Leona M. and Harry B. Helmsley Charitable Trust
DOI 10.1016/j.jaci.2022.08.030
WOS ID 000955856300001
Scopus ID 85149072882
PubMed ID 36462956
Erfassungsdatum 2022-12-08
[➜Korrektur melden]