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001-es BibID:	BIBFORM013546
Első szerző:	Picard, Capucine
Cím:	Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency / Capucine Picard, Horst von Bernuth, Pegah Ghandil, Maya Chrabieh,Ofer Levy, Peter D. Arkwright, Douglas McDonald, Raif S. Geha,Hidetoshi Takada, Jens C. Krause, C. Buddy Creech, Cheng-Lung Ku, Stephan Ehl, László Maródi, Saleh Al-Muhsen, Sami Al-Hajjar, Abdulaziz Al-Ghonaium, Noorbibi K. Day-Good, Steven M. Holland, John I. Gallin,Helen Chapel, David P. Speert, Carlos Rodriguez-Gallego, Elena Colino, Ben-Zion Garty, Chaim Roifman, Toshiro Hara, Hideto Yoshikawa, Shigeaki Nonoyama, Joseph Domachowske, Andrew C. Issekutz, Mimi Tang, Joanne Smart, Simona Eva Zitnik, Cyrille Hoarau, Dinakantha S. Kumararatne, Adrian J. Thrasher, E. Graham Davies, Claire Bethune, Nicolas Sirvent, Dominique de Ricaud, Yildiz Camcioglu, Júlia Vasconcelos, Margarida Guedes, Artur Bonito Vitor, Carlos Rodrigo, Francisco Almazán, Maria Méndez, Juan Ignacio Aróstegui, Laia Alsina, Claudia Fortuny, Janine Reichenbach, James W. Verbsky, Xavier Bossuyt, Rainer Doffinger, Laurent Abel, Anne Puel, and Jean-Laurent Casanova
Dátum:	2010
ISSN:	0025-7974
Tárgyszavak:	Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:	Medicine. - 89 : 6 (2010), p. 403-425. -
További szerzők:	Bernuth, Horst von Ghandil, Pegah Chrabieh, Maya Levy, Ofer Arkwright, Peter D. McDonald, Douglas Geha, Raif S. Takada, Hidetoshi Krause, Jens Creech, C. Buddy Ku, Cheng-Lung Ehl, Stephan Maródi László (1949-) (gyermekgyógyász infektológus, immunológus) Al-Muhsen, Saleh Al-Hajjar, Sami Al-Ghonaium, Abdulaziz Day-Good, Noorbibi K. Holland, Steven M. Gallin, John Chapel, Helen Speert, David Rodriguez-Gallego, Carlos Colino, Elena Garty, Ben-Zion Roifman, Chaim Hara, Toshiro Yoshikawa, Hideto Nonoyama, Shigeaki Domachowske, Joseph Issekutz, Andrew C. Tang, Mimi Smart, Joanne Zitnik, Simona Eva Hoarau, Cyrille Kumararatne, Dinakantha S. Thrasher, Adrian J. Davies, Graham Bethune, Claire Sirvent, Nicolas de Ricaud, Dominique Camcioglu, Yildiz Vasconcelos, Julia Guedes, Margarida Bonito Vitor, Artur Rodrigo, Carlos Almazán, Francisco Méndez, Maria Aróstegui, Juan Ignacio Alsina, Laia Fortuny, Claudia Reichenbach, Jeanine Verbsky, James W. Bossuyt, Xavier Doffinger, Rainer Abel, Laurent Puel, Anne Casanova, Jean-Laurent
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001-es BibID:	BIBFORM013867
Első szerző:	Puel, Anne
Cím:	Autoantibodies against to IL-17A, IL-17F and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I / Anne Puel, Rainer Döffinger, Angels Natividad, Maya Chrabieh, Gabriela Barcenas-Morales, Capucine Picard, Aurélie Cobat, Marie Ouachée-Chardin, Antoine Toulon, Jacinta Bustamante, Saleh Al-Muhsen, Mohammed Al-Owain, Peter D. Arkwright, Colm Costigan, Vivienne McConnell, Andrew J. Cant, Mario Abinun, Michel Polak, Pierre-Francois Bougneres, Dinakantha Kumararatne, László Marodi, Amit Nahum, Chaim Roifman, Stéphane Blanche, Alain Fischer, Christine Bodemer, Laurent Abel, Desa Lilic, Jean-Laurent Casanova
Dátum:	2010
ISSN:	0022-1007
Megjegyzések:	Most patients with autoimmune polyendocrine syndrome type I (APS-I) display chronic mucocutaneous candidiasis (CMC). We hypothesized that this CMC might result from autoimmunity to interleukin (IL)-17 cytokines. We found high titers of autoantibodies (auto-Abs) against IL-17A, IL-17F, and/or IL-22 in the sera of all 33 patients tested, as detected by multiplex particle-based flow cytometry. The auto-Abs against IL-17A, IL-17F, and IL-22 were specific in the five patients tested, as shown by Western blotting. The auto-Abs against IL-17A were neutralizing in the only patient tested, as shown by bioassays of IL-17A activity. None of the 37 healthy controls and none of the 103 patients with other autoimmune disorders tested had such auto-Abs. None of the patients with APS-I had auto-Abs against cytokines previously shown to cause other welldefined clinical syndromes in other patients (IL-6, interferon [IFN]-gamma, or granulocyte/macrophage colony-stimulating factor) or against other cytokines (IL-1beta, IL-10, IL-12, IL-18, IL-21, IL-23, IL-26, IFN-beta, tumor necrosis factor [alfa], or transforming growth factor beta). These findings suggest that auto-Abs against IL-17A, IL-17F, and IL-22 may cause CMC in patients with APS-I.
Tárgyszavak:	Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:	Journal of Experimental Medicine. - 207 : 2 (2010), p. 291-297. -
További szerzők:	Döffinger, Rainer Natividad, Angels Chrabieh, Maya Barcenas-Morales, Gabriela Picard, Capucine Cobat, Aurélie Ouachée-Chardin, Marie Toulon, Antoine Bustamante, Jacinta Al-Muhsen, Saleh Al-Owain, Mohammed Arkwright, Peter D. Costigan, Colm McConnell, Vivienne Cant, Andrew J. Abinun, Mario Polak, Michel Bougnéres, Pierre-Francois Kumararatne, Dinakantha S. Maródi László (1949-) (gyermekgyógyász infektológus, immunológus) Nahum, Amit Roifman, Chaim Blanche, Stéphane Fischer, Alain Bodemer, Christine Abel, Laurent Lilic, Desa Casanova, Jean-Laurent
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