Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/11401
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Type: Journal article
Title: Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
Author: McDermott, M.
Aksentijevich, I.
Galon, J.
McDermott, E.
Ogunkolade, B.
Centola, M.
Mansfield, E.
Gadina, M.
Karenko, L.
Petterson, T.
McCarthy, J.
Frucht, D.
Aringer, M.
Torosyan, Y.
Teppo, A.
Wilson, M.
Karaarslan, H.
Wan, Y.
Todd, I.
Wood, G.
et al.
Citation: Cell, 1999; 97(1):133-144
Publisher: CELL PRESS
Issue Date: 1999
ISSN: 0092-8674
1097-4172
Abstract: Autosomal dominant periodic fever syndromes are characterized by unexplained episodes of fever and severe localized inflammation. In seven affected families, we found six different missense mutations of the 55 kDa tumor necrosis factor receptor (TNFR1), five of which disrupt conserved extracellular disulfide bonds. Soluble plasma TNFR1 levels in patients were approximately half normal. Leukocytes bearing a C52F mutation showed increased membrane TNFR1 and reduced receptor cleavage following stimulation. We propose that the autoinflammatory phenotype results from impaired downregulation of membrane TNFR1 and diminished shedding of potentially antagonistic soluble receptor. TNFR1-associated periodic syndromes (TRAPS) establish an important class of mutations in TNF receptors. Detailed analysis of one such mutation suggests impaired cytokine receptor clearance as a novel mechanism of disease.
Keywords: Leukocytes; Humans; Familial Mediterranean Fever; Syndrome; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Antigens, CD; Pedigree; DNA Mutational Analysis; Amino Acid Sequence; Genes, Dominant; Germ-Line Mutation; Molecular Sequence Data; Female; Male
RMID: 0030004338
DOI: 10.1016/S0092-8674(00)80721-7
Appears in Collections:Genetics publications

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