3,909 research outputs found
Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutières Syndrome with severe end-organ involvement
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 23/03/2022
- Field of study
Serum proteomics reveals hemophagocytic lymphohistiocytosis-like phenotype in a subset of patients with multisystem inflammatory syndrome in children
- Author
- Bannier Michiel A.G.E.
- Bekhof Jolita
- Breukels Mijke
- Buddingh Emilie P.
- Buysse Corinne M.P.
- Haerynck Filomeen
- Hammer Sanne C.
- Holierhoek Marloes G.
- Hoste Levi
- Jacobs Monique A.M.
- Jansen-Hoogendijk Anja M.
- Kamps Arvid W.A.
- Lebon Ankie
- Lugthart Gertjan
- Oostenbrink Rianne
- Oudshoorn Johanna H.
- Tavernier Simon J.
- Terheggen-Lagro Suzanne W.J.
- Tramper-Stranders Gerdien A.
- Tulling Adam J.
- van den Akker Erik B.
- van der Linden Jan W.
- van Gijn Marielle E.
- Vastert Sebastiaan J.
- von Asmuth Erik G.J.
- Wieringa Jantien W.
- Wildenbeest Joanne G.
- Publication venue
- Publication date
- 01/07/2024
- Field of study
Children with Multisystem Inflammatory Syndrome in Children (MIS-C) can present with thrombocytopenia, which is a key feature of hemophagocytic lymphohistiocytosis (HLH). We hypothesized that thrombocytopenic MIS-C patients have more features of HLH. Clinical characteristics and routine laboratory parameters were collected from 228 MIS-C patients, of whom 85 (37%) were thrombocytopenic. Thrombocytopenic patients had increased ferritin levels; reduced leukocyte subsets; and elevated levels of ASAT and ALAT. Soluble IL-2RA was higher in thrombocytopenic children than in non-thrombocytopenic children. T-cell activation, TNF-alpha and IFN-gamma signaling markers were inversely correlated with thrombocyte levels, consistent with a more pronounced cytokine storm syndrome. Thrombocytopenia was not associated with severity of MIS-C and no pathogenic variants were identified in HLH-related genes. This suggests that thrombocytopenia in MIS-C is not a feature of a more severe disease phenotype, but the consequence of a distinct hyperinflammatory immunopathological process in a subset of children.</p
Serum proteomics reveals hemophagocytic lymphohistiocytosis-like phenotype in a subset of patients with multisystem inflammatory syndrome in children
- Author
- Bannier Michiel A.G.E.
- Bekhof Jolita
- Breukels Mijke
- Buddingh Emilie P.
- Buysse Corinne M.P.
- Haerynck Filomeen
- Hammer Sanne C.
- Holierhoek Marloes G.
- Hoste Levi
- Jacobs Monique A.M.
- Jansen-Hoogendijk Anja M.
- Kamps Arvid W.A.
- Lebon Ankie
- Lugthart Gertjan
- Oostenbrink Rianne
- Oudshoorn Johanna H.
- Tavernier Simon J.
- Terheggen-Lagro Suzanne W.J.
- Tramper-Stranders Gerdien A.
- Tulling Adam J.
- van den Akker Erik B.
- van der Linden Jan W.
- van Gijn Marielle E.
- Vastert Sebastiaan J.
- von Asmuth Erik G.J.
- Wieringa Jantien W.
- Wildenbeest Joanne G.
- Publication venue
- Publication date
- 01/07/2024
- Field of study
Children with Multisystem Inflammatory Syndrome in Children (MIS-C) can present with thrombocytopenia, which is a key feature of hemophagocytic lymphohistiocytosis (HLH). We hypothesized that thrombocytopenic MIS-C patients have more features of HLH. Clinical characteristics and routine laboratory parameters were collected from 228 MIS-C patients, of whom 85 (37%) were thrombocytopenic. Thrombocytopenic patients had increased ferritin levels; reduced leukocyte subsets; and elevated levels of ASAT and ALAT. Soluble IL-2RA was higher in thrombocytopenic children than in non-thrombocytopenic children. T-cell activation, TNF-alpha and IFN-gamma signaling markers were inversely correlated with thrombocyte levels, consistent with a more pronounced cytokine storm syndrome. Thrombocytopenia was not associated with severity of MIS-C and no pathogenic variants were identified in HLH-related genes. This suggests that thrombocytopenia in MIS-C is not a feature of a more severe disease phenotype, but the consequence of a distinct hyperinflammatory immunopathological process in a subset of children.</p
Nutrition, diet and immunosenescence
- Author
- Agrawal
- Agrawal
- Akbar
- Almanzar
- Alonso
- Alperovich
- Alvarez-Rodriguez
- Arunachalam
- Azzini
- Bates
- Bechoua
- Belisle
- Belisle
- Berzins
- Blomberg
- Bogden
- Borrego
- Bouwens
- Bravo
- Buffa
- Bunout
- Butcher
- Calder
- Camous
- Canaday
- Cannizzo
- Carluccio
- Castle
- Cevenini
- Chandra
- Chatta
- Chidrawar
- Chung
- Ciaramella
- Clambey
- Clark
- Claudio Nicoletti
- Colonna-Romano
- Corridan
- Corsini
- Cortes
- Cossack
- Currier
- De La Fuente
- De la Fuente
- De la Fuente
- De Martinis
- DelaRosa
- DelaRosa
- Della Bella
- DellâAgli
- Dewan
- Di Lorenzo
- Dong
- Donnini
- Dorshkind
- Dubey
- Duchateau
- Dunn-Walters
- Effros
- Enos
- Estruch
- Farges
- Fateh
- Faunce
- Fearnley
- Feart
- Fietta
- Flores
- Fortes
- Fortin
- Fortin
- Franceschi
- Franceschi
- Frasca
- Frasca
- Fulop
- Fulop
- Fulop
- Fulop
- Galli
- Gao
- Gayoso
- Gebremichael
- Gibson
- Gibson
- Gill
- Gill
- Ginaldi
- Gomez
- Goronzy
- Goronzy
- Guigoz
- Guigoz
- Hadziabdic
- Hakim
- Hamilton-Miller
- Haynes
- Haynes
- Haynes
- Herndler-Brandstetter
- Herrero
- Herrero
- Hilmer
- Hodkinson
- Hong
- Ishimoto
- Jing
- Kahmann
- Kamal Ivory
- Khan
- Kowdley
- Larbi
- Larbi
- Lasheras
- Le Garff-Tavernier
- Lee
- Lesourd
- Lesourd
- Ligthart
- Lung
- Magrone
- Mariani
- Mariani
- Martinez-Gonzalez
- Maue
- McElhaney
- Merchant
- Meydani
- Meydani
- Meydani
- Meydani
- Mitchell
- Monagas
- Murasko
- Mysliwska
- Mònica Maijó
- Nagel
- Nicoletti
- Nicoletti
- Nikolich-Zugich
- Nova
- Nova
- Ogawa
- Ogawa
- Osler
- Ouwehand
- Ouwehand
- Pae
- Paganelli
- Pallast
- Pawelec
- Peralbo
- Peralbo
- Pfister
- Plackett
- Plowden
- Prakash
- Prasad
- Prasad
- Prasad
- Prasad
- Psaltopoulou
- PĂŠrez-Cabezas
- Rees
- Rink
- Salas-Salvado
- Sarah J. Clements
- Saule
- Saurwein-Teissl
- Scarmeas
- Scarmeas
- Schenkein
- Schiffrin
- Schiffrin
- Schwaiger
- Shaw
- Shodell
- Simon R. Carding
- Sofi
- Sofi
- Solana
- Solana
- Solana
- Sridharan
- Steger
- Stout-Delgado
- Swift
- Tangney
- Tasat
- Tortorella
- Tortorella
- Trichopoulou
- Uyemura
- Valls-Pedret
- van Duin
- Varas
- Vasto
- Vasto
- Vetvicka
- Vulevic
- Waitzberg
- Wallace
- Watson
- Webster
- Weiskopf
- Weksler
- Wenisch
- Wikby
- Willett
- Wong
- Wordsworth
- Wu
- Yaqoob
- Yaqoob
- Yuan
- Zanni
- Zissel
- Publication venue
- 'Elsevier BV'
- Publication date
- 25/12/2013
- Field of study
Ageing is characterized by immunosenescence and the progressive decline in immunity in association with an increased frequency of infections and chronic disease. This complex process affects both the innate and adaptive immune systems with a progressive decline in most immune cell populations and defects in activation resulting in loss of function. Although host genetics and environmental factors, such as stress, exercise and diet can impact on the onset or course of immunosenescence, the mechanisms involved are largely unknown. This review focusses on identifying the most significant aspects of immunosenescence and on the evidence that nutritional intervention might delay this process, and consequently improve the quality of life of the elderly
Compressed representation of a partially defined integer function over multiple arguments
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdelalim AA
- Abdullin S
- Abdulsalam A
- Acosta D
- Acosta MV
- Adair A
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adzic P
- Agram J-L
- Aguilar-Benitez M
- Ahmad M
- Ahmad WH
- Ahuja S
- Akchurin N
- Akgun B
- Akgun U
- Akin IV
- Alagoz E
- Albajar C
- Albayrak EA
- Albergo S
- Albrow M
- Alcaraz Maestre J
- Alda Junior WL
- Alderweireldt S
- Alexander J
- Aliev T
- Alimena J
- Almeida N
- Alverson G
- Alves GA
- Amapane N
- Amsler C
- Anagnostou G
- Anastassov A
- Anderson J
- Andrea J
- Andreev V
- Andreev V
- Andreev Y
- Andrews W
- Androsov K
- Antonelli L
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Apresyan A
- Apyan A
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arneodo M
- Arora S
- Asavapibhop B
- Asawatangtrakuldee C
- Asghar MI
- Asin I
- Askew A
- Aslanoglou X
- Assran Y
- Ata M
- Attikis A
- Auffray E
- Autermann C
- Auzinger G
- Avdeeva E
- Avery P
- Avetisyan A
- Avila C
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzolini V
- Azzurri P
- Baarmand MM
- Babb J
- Bacchetta N
- Bachmair F
- Bachtis M
- Baden A
- Baeni L
- Baffioni S
- Bagliesi G
- Bahtiyar H
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Ball AH
- Ban Y
- Banerjee S
- Banerjee S
- Bansal M
- Bansal S
- Barbagli G
- Barberis E
- Barbone L
- Barfuss AF
- Bargassa P
- Barge D
- Baringer P
- Barker A
- Barlas E
- Barnett BA
- Barney D
- Barone L
- Bartalini P
- Barth C
- Bartosik N
- Basegmez S
- Basso L
- Battilana C
- Bauer G
- Bauerdick LAT
- Baumgartel D
- Baus C
- Bayshev I
- Bazterra VE
- Bean A
- Beauceron S
- Beaudette F
- Beaupere N
- Beernaert K
- Behr J
- Behrenhoff W
- Behrens U
- Beirao Da Cruz E Silva C
- Belforte S
- Beliy N
- Belknap DA
- Bell AJ
- Bell KW
- Bellan R
- Beluffi C
- Belyaev A
- Belyaev A
- Benaglia A
- Bencze G
- Bendavid J
- Benedetti D
- Benelli G
- Benhabib L
- Beni N
- Benitez JF
- Benucci L
- Benussi L
- Benvenuti AC
- Beranek S
- Beretvas A
- Bergauer T
- Berger J
- Bergholz M
- Beri SB
- Bernardes CA
- Bernardini J
- Bernet C
- Berry D
- Berry E
- Berryhill J
- Bertl W
- Besancon M
- Betchart B
- Bethani A
- Betts RR
- Bhardwaj A
- Bhat PC
- Bhatnagar V
- Bhattacharya S
- Bhattacharya S
- Bhatti A
- Bialkowska H
- Bian JG
- Bianchi G
- Bianchini L
- Bianco S
- Biasini M
- Biino C
- Bilei GM
- Bilin B
- Bilki B
- Bilmis S
- Bisello D
- Bitioukov S
- Blekman F
- Blobel V
- Bloch D
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- Bloom K
- Bluj M
- Blumenfeld B
- Blyweert S
- Boccali T
- Bocci A
- Bochenek J
- Bodek A
- Bodin D
- Boeser C
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- Bolognesi S
- Bonacorsi D
- Bonato A
- Bondu O
- Boos E
- Bornheim A
- Borras K
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- Bortignon P
- Bortoletto D
- Bose S
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- Botta C
- Boudoul G
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- Bourilkov D
- Boutle S
- Braibant-Giacomelli S
- Branca A
- Branson JG
- Breedon R
- Breto G
- Breuker H
- Brew C
- Brigliadori L
- Brigljevic V
- Brinkerhoff A
- Broccolo G
- Brochero Cifuentes JA
- Brochet S
- Brom J-M
- Brona G
- Brooke JJ
- Brown RM
- Brownson E
- Brun H
- Bruno G
- Bryer AG
- Buchmann MA
- Buchmuller O
- Bucinskaite I
- Bunichev V
- Bunin P
- Bunkowski K
- Bunn J
- Buontempo S
- Burgmeier A
- Burkett K
- Burton D
- Busson P
- Busza W
- Butler JN
- Butler PH
- Butt J
- Butz E
- Bylsma B
- Cabrillo IJ
- Caebergs T
- Cakir A
- Calabria C
- Calamba A
- Calderon De La Barca Sanchez M
- Calderon A
- Cali IA
- Calligaris L
- Callner J
- Calpas B
- Calvert B
- Calvo E
- Campagnari C
- Campanini R
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- Candelise V
- Cankocak K
- Capiluppi P
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- Carlsmith D
- Carrillo Montoya CA
- Carrillo Moreno S
- Carroll R
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- Casimiro Linares E
- Castaldi R
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- Castro A
- Caudron A
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- Cavallari F
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- Ceballos GG
- Cepeda M
- Cerati GB
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- Cerizza G
- Cerminara G
- Cerrada M
- Chabert EC
- Chadwick M
- Chakaberia I
- Chamizo Llatas M
- Chan KM
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- Chang P
- Chang S
- Chang YH
- Chang YW
- Chanon N
- Chao Y
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- Chatterjee A
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- Choudhary BC
- Choudhury S
- Christiansen T
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- Chwalek T
- Ciesielski R
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- Cimmino A
- Cipriano PMR
- Cittolin S
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- Civinini C
- Claes DR
- Clare R
- Clarida W
- Clement E
- Clerbaux B
- Cline D
- CMS Collaboration
- Coarasa Perez JA
- Cockerill DJA
- Colafranceschi S
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- Cooper SI
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- Costa M
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- Costantini S
- Costanza F
- Couderc F
- Coughlan JA
- Cousins R
- Covarelli R
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- Cox PT
- Creanza D
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- Cripps N
- Cuevas J
- Cuffiani M
- Cumalat JP
- Cussans D
- Custodio A
- Cutajar M
- Cutts D
- Cwiok M
- Czellar S
- D'Agnolo RT
- D'Alessandro R
- D'Alfonso M
- d'Enterria D
- D'Hondt J
- Da Costa EM
- Dabrowski A
- Daci N
- Dahmes B
- Dahms T
- Dalchenko M
- Dallavalle GM
- Damgov J
- Danielson T
- Das S
- Daskalakis G
- Dasu S
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- Dauncey P
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- Davies G
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- De La Cruz B
- De La Cruz-Burelo E
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- de Monchenault GH
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- De Roeck A
- de Troconiz JF
- De Visscher S
- De Wolf EA
- Deisher A
- Deiters K
- Dejardin M
- del Arbol PMR
- Del Re D
- Delaere C
- Delannoy AG
- Delgado Peris A
- Dell'Orso R
- Della Negra M
- Della Ricca G
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- Demina R
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- Denegri D
- Deniz M
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- Dermenev A
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- Di Giovanni GP
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- Dumanoglu I
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- Duric S
- Durkin LS
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- Dutta D
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- Eckerlin G
- Ecklund KM
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- Elvira VD
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- Evangelou I
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- Fabbricatore P
- Fabbro B
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- Fabozzi F
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- Fahim A
- Fanfani A
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- Fantasia C
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- Fanzago F
- Farrell C
- Fasanella D
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- Fedi G
- Fehling D
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- Ferapontov A
- Ferbel T
- Ferencek D
- Ferguson T
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- Fernandez Menendez J
- Fernandez Perez Tomei TR
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- Ferreira Parracho PG
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- Fisk I
- Flacher H
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- Focardi E
- Folgueras S
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- Foudas C
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- Franzoni G
- Frazier R
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- Freudenreich K
- Friedl M
- Friis E
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- Frueboes T
- Fruehwirth R
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- Furic IK
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- Georgiou G
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- Gerber CE
- Gershtein Y
- Geurts FJM
- Ghete VM
- Ghezzi A
- Ghosh S
- Giacomelli P
- Giammanco A
- Giassi A
- Gibbons LK
- Giffels M
- Gigi D
- Gilbert A
- Gill K
- Gilmore J
- Giordano D
- Giordano F
- Girgis S
- Girone M
- Giubilato P
- Giunta M
- Giurgiu G
- Givernaud A
- Glege F
- Gleyzer SV
- Glushkov I
- Gninenko S
- Gobbo B
- Godinovic N
- Godshalk A
- Goerlach U
- Goerner M
- Goetzmann C
- Goh J
- Gokbulut G
- Goldenzweig P
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- Gollapinni S
- Golovtsov V
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- Gomez Moreno B
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- Gomez JP
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- Goncharov M
- Gonzalez Caballero I
- Gonzalez Lopez O
- Gonzalez Sanchez J
- Gonzalez JS
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- Goodell J
- Gorbunov I
- Gori V
- Gorski M
- Gosselink M
- Gottschalk E
- Goulianos K
- Gouskos L
- Gouzevitch M
- Govoni P
- Gowdy S
- Goy Lopez S
- Gozzelino A
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- Grandi C
- Gras P
- Grassi M
- Gray L
- Gray R
- Graziano A
- Green D
- Greene S
- Gregores EM
- Gribushin A
- Griffiths S
- Grigelionis I
- Grimes M
- Grippo MT
- Gritsan AV
- Gronberg J
- Grothe M
- Grundler U
- Grunewald M
- Guchait M
- Gude A
- Gueth A
- Guida R
- Guiducci L
- Guler AM
- Gulmez E
- Gunaydin YO
- Gunnellini P
- Guo Y
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- Guragain S
- Gurpinar E
- Gurrola A
- Gurtu A
- Guthoff M
- Gutsche O
- Gyun D
- Haas J
- Habib S
- Hadjiiska R
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- Publication venue
- Publication date
- 01/01/2013
- Field of study
In OLAP (OnLine Analitical Processing) data are analysed in an n-dimensional cube. The cube may be represented as a partially defined function over n arguments. Considering that often the function is not defined everywhere, we ask: is there a known way of representing the function or the points in which it is defined, in a more compact manner than the trivial one
X-ray emission from the Sombrero galaxy: discrete sources
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
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- Wood JS
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- Wulz CE
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- Wyslouch B
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- Yi K
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- Yilmaz Y
- Yohay R
- Yoo HD
- Yoon AS
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- Yumiceva F
- Yun JC
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- Zabi A
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- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zang SL
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
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- Zhang Z
- Zheng Y
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- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
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- Zoeller MH
- Zorbilmez C
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2010
- Field of study
We present a study of discrete X-ray sources in and around the
bulge-dominated, massive Sa galaxy, Sombrero (M104), based on new and archival
Chandra observations with a total exposure of ~200 ks. With a detection limit
of L_X = 1E37 erg/s and a field of view covering a galactocentric radius of ~30
kpc (11.5 arcminute), 383 sources are detected. Cross-correlation with Spitler
et al.'s catalogue of Sombrero globular clusters (GCs) identified from HST/ACS
observations reveals 41 X-rays sources in GCs, presumably low-mass X-ray
binaries (LMXBs). We quantify the differential luminosity functions (LFs) for
both the detected GC and field LMXBs, whose power-low indices (~1.1 for the
GC-LF and ~1.6 for field-LF) are consistent with previous studies for
elliptical galaxies. With precise sky positions of the GCs without a detected
X-ray source, we further quantify, through a fluctuation analysis, the GC LF at
fainter luminosities down to 1E35 erg/s. The derived index rules out a
faint-end slope flatter than 1.1 at a 2 sigma significance, contrary to recent
findings in several elliptical galaxies and the bulge of M31. On the other
hand, the 2-6 keV unresolved emission places a tight constraint on the field
LF, implying a flattened index of ~1.0 below 1E37 erg/s. We also detect 101
sources in the halo of Sombrero. The presence of these sources cannot be
interpreted as galactic LMXBs whose spatial distribution empirically follows
the starlight. Their number is also higher than the expected number of cosmic
AGNs (52+/-11 [1 sigma]) whose surface density is constrained by deep X-ray
surveys. We suggest that either the cosmic X-ray background is unusually high
in the direction of Sombrero, or a distinct population of X-ray sources is
present in the halo of Sombrero.Comment: 11 figures, 5 tables, ApJ in pres
Performance of the CMS Cathode Strip Chambers with Cosmic Rays
- Author
- Abadjiev K
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abelev B
- Acosta D
- Acosta JG
- Acosta MV
- Actis O
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adolphi R
- Adzic P
- Afaq MA
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahmed W
- Ahuja S
- Aisa D
- Aisa S
- Akchurin N
- Akgun B
- Akgun U
- Akimenko S
- Akin IV
- Alagoz E
- Alampi G
- Albajar C
- Albayrak EA
- Alberdi J
- Albergo S
- Albert E
- Albrow M
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- Zachariadou A
- Zalewski P
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- Zanetti M
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- Zeidler C
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- Zelepoukine S
- Zeuner WD
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- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2009
- Field of study
The Cathode Strip Chambers (CSCs) constitute the primary muon tracking device
in the CMS endcaps. Their performance has been evaluated using data taken
during a cosmic ray run in fall 2008. Measured noise levels are low, with the
number of noisy channels well below 1%. Coordinate resolution was measured for
all types of chambers, and fall in the range 47 microns to 243 microns. The
efficiencies for local charged track triggers, for hit and for segments
reconstruction were measured, and are above 99%. The timing resolution per
layer is approximately 5 ns
Performance and Operation of the CMS Electromagnetic Calorimeter
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- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/1
- Field of study
The operation and general performance of the CMS electromagnetic calorimeter
using cosmic-ray muons are described. These muons were recorded after the
closure of the CMS detector in late 2008. The calorimeter is made of lead
tungstate crystals and the overall status of the 75848 channels corresponding
to the barrel and endcap detectors is reported. The stability of crucial
operational parameters, such as high voltage, temperature and electronic noise,
is summarised and the performance of the light monitoring system is presented
Unsupervised High-Dimensional Analysis Aligns Dendritic Cells across Tissues and Species.
- Author
- Bogen Bjarne
- Chakarov Svetoslav
- Chan Dedrick Kok Hong
- Chan Jerry Kok Yen
- Chen Jinmiao
- Choolani Mahesh
- Chung Tam John Kit
- De Prijck Sofie
- Dutertre Charles-Antoine
- Fossum Even
- Ginhoux Florent
- Guilliams Martin
- Henri Sandrine
- Hon Tony Lim Kiat
- Irac Sergio Erdal
- Lambrecht Bart N
- Larbi Anis
- Low Gillian Hui Ling
- Low Ivy
- Luche HervĂŠ
- Malissen Bernard
- Mattar Citra Nurfarah
- McGovern Naomi
- Newell Evan William
- Poidinger Michael
- Saeys Yvan
- Scott Charlotte L
- Sichien Dorine
- Sumatoh Hermi Rizal
- Tan Ker Kan
- Tavernier Simon J
- Van Gassen Sofie
- Publication venue
- Immunity
- Publication date
- 01/01/2016
- Field of study
Dendritic cells (DCs) are professional antigen-presenting cells that hold great therapeutic potential. Multiple DC subsets have been described, and it remains challenging to align them across tissues and species to analyze their function in the absence of macrophage contamination. Here, we provide and validate a universal toolbox for the automated identification of DCs through unsupervised analysis of conventional flow cytometry and mass cytometry data obtained from multiple mouse, macaque, and human tissues. The use of a minimal set of lineage-imprinted markers was sufficient to subdivide DCs into conventional type 1 (cDC1s), conventional type 2 (cDC2s), and plasmacytoid DCs (pDCs) across tissues and species. This way, a large number of additional markers can still be used to further characterize the heterogeneity of DCs across tissues and during inflammation. This framework represents the way forward to a universal, high-throughput, and standardized analysis of DC populations from mutant mice and human patients
The ubiquitin-editing enzyme A20 controls NK cell homeostasis through regulation of mTOR activity and TNF
- Author
- Boon L. (Louis)
- Deswarte K. (Kim)
- Fayazpour F.
- Heerswynghels M. (Manon) van
- Janssens S. (Sophie)
- Lambrecht B.N.M. (Bart)
- Loo G. (Geert) van
- Martens A.
- Prijck S. (Sofie) de
- Takahashi N. (Nozomi)
- Tavernier S.J. (Simon)
- van Helden MJ
- van Moorleghem J.
- Vandenabeele P. (Peter)
- Vergote K
- Vetters J. (Jessica)
- Vivier E. (Eric)
- Wahlen S.
- Publication venue
- 'Rockefeller University Press'
- Publication date
- 01/01/2019
- Field of study
The ubiquitin-editing enzyme A20 is a well-known regulator of immune cell function and homeostasis. In addition, A20
protects cells from death in an ill-defined manner. While most studies focus on its role in the TNF-receptor complex, we here
identify a novel component in the A20-mediated decision between life and death. Loss of A20 in NK cells led to spontaneous
NK cell death and severe NK cell lymphopenia. The few remaining NK cells showed an immature, hyperactivated phenotype,
hallmarked by the basal release of cytokines and cytotoxic molecules. NK-A20â/â cells were hypersensitive to TNF-induced cell
death and could be rescued, at least partially, by a combined deficiency with TNF. Unexpectedly, rapamycin, a wellestablished inhibitor of mTOR, also strongly protected NK-A20â/â cells from death, and further studies revealed that A20
restricts mTOR activation in NK cells. This study therefore maps A20 as a crucial regulator of mTOR signaling and underscores
the need for a tightly balanced mTOR pathway in NK cell homeostasis
- âŚ