37 research outputs found
Recommended from our members
Temporal Proteomic Analysis of BK Polyomavirus Infection Reveals Virus-Induced G2 Arrest and Highly Effective Evasion of Innate Immune Sensing.
- Publication venue
- J Virol
- Publication date
- 15/08/2019
- Field of study
BK polyomavirus (BKPyV) is a small DNA virus that establishes a life-long persistent infection in the urinary tract of most people. BKPyV is known to cause severe morbidity in renal transplant recipients and can lead to graft rejection. The simple 5.2-kbp double-stranded DNA (dsDNA) genome expresses just seven known proteins; thus, it relies heavily on the host machinery to replicate. How the host proteome changes over the course of infection is key to understanding this host-virus interplay. Here, for the first time quantitative temporal viromics has been used to quantify global changes in >9,000 host proteins in two types of primary human epithelial cells throughout 72âh of BKPyV infection. These data demonstrate the importance of cell cycle progression and pseudo-G2 arrest in effective BKPyV replication, along with a surprising lack of an innate immune response throughout the whole virus replication cycle. BKPyV thus evades pathogen recognition to prevent activation of innate immune responses in a sophisticated manner.IMPORTANCE BK polyomavirus can cause serious problems in immune-suppressed patients, in particular, kidney transplant recipients who can develop polyomavirus-associated kidney disease. In this work, we have used advanced proteomics techniques to determine the changes to protein expression caused by infection of two independent primary cell types of the human urinary tract (kidney and bladder) throughout the replication cycle of this virus. Our findings have uncovered new details of a specific form of cell cycle arrest caused by this virus, and, importantly, we have identified that this virus has a remarkable ability to evade detection by host cell defense systems. In addition, our data provide an important resource for the future study of kidney epithelial cells and their infection by urinary tract pathogens.Isaac Newton Trust (part funding of ISSF award to C.M.C.
Human neutrophil clearance of bacterial pathogens triggers anti-microbial gamma delta T cell responses in early infection
- Author
- A Boëdec
- A Matsushima
- A Reichenberg
- AC Brown
- AC Hayday
- AC Hayday
- Amanda C. Brown
- B Altincicek
- B Moser
- Bernhard Moser
- C Agrati
- C Belmant
- C De Santo
- C MĂŒnz
- CC Szeto
- Chan-Yu Lin
- CM Bunke
- Colin Hill
- Cormac G. M. Gahan
- CT Morita
- CT Spencer
- CT Weaver
- D Vermijlen
- David W. Johnson
- DI Godfrey
- DJ Pennington
- DK Kim
- E Oldfield
- E. John Wherry
- F Annunziato
- F Dieli
- F Sallusto
- G Sarikonda
- Gareth W. Roberts
- GW Roberts
- H Jomaa
- H Jomaa
- H Li
- H Wang
- H Wei
- I MĂŒller
- J Feurle
- J Mookerjee-Basu
- James A. Chess
- JF Bukowski
- JJ O'Shea
- John D. Williams
- JS Savill
- K Pietschmann
- KJ Puan
- KK Kumarasamy
- KM Murphy
- L Troidle
- M Begley
- M Begley
- M Blunden
- M Bonneville
- M Brandes
- M Eberl
- M Eberl
- M Eberl
- M Eberl
- M Eberl
- M Fahim
- M Kistowska
- M Krishnan
- M Pelletier
- M Rohmer
- MA Missinou
- Mark A. Toleman
- Martin S. Davey
- Matthias Eberl
- MC Devilder
- MC Devilder
- MI Hirsh
- MJ Llewelyn
- N Nathan
- N Topley
- Nicholas Topley
- O Devuyst
- P Choi
- P Constant
- PS Evans
- R Medzhitov
- RE Rojas
- RM McLoughlin
- S Amslinger
- S Mujais
- Simon J. Davies
- Sinéad Heuston
- SJ Davies
- SM Hurst
- SR Gill
- T Ganz
- Tanya Parish
- TR Walsh
- TW Rice
- W Holtmeier
- Y Kato
- Y Neu
- Y Tanaka
- Y Zhang
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2011
- Field of study
Human blood Vc9/Vd2 T cells, monocytes and neutrophils share a responsiveness toward inflammatory chemokines and are rapidly recruited to sites of infection. Studying their interaction in vitro and relating these findings to in vivo observations in patients may therefore provide crucial insight into inflammatory events. Our present data demonstrate that Vc9/Vd2 T cells provide potent survival signals resulting in neutrophil activation and the release of the neutrophil chemoattractant CXCL8 (IL-8). In turn, Vc9/Vd2 T cells readily respond to neutrophils harboring phagocytosed bacteria, as evidenced by expression of CD69, interferon (IFN)-c and tumor necrosis factor (TNF)-a. This response is dependent on the ability of these bacteria to produce the microbial metabolite (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate (HMB-PP), requires cell-cell contact of Vc9/Vd2 T cells with accessory monocytes through lymphocyte function-associated antigen-1 (LFA-1), and results in a TNF-a dependent proliferation of Vc9/Vd2 T cells. The antibiotic fosmidomycin, which targets the HMB-PP biosynthesis pathway, not only has a direct antibacterial effect on most HMB-PP producing bacteria but also possesses rapid anti-inflammatory properties by inhibiting cd T cell responses in vitro. Patients with acute peritoneal-dialysis (PD)-associated bacterial peritonitis â characterized by an excessive influx of neutrophils and monocytes into the peritoneal cavity â show a selective activation of local Vc9/Vd2 T cells by HMB-PP producing but not by HMB-PP deficient bacterial pathogens. The cd T celldriven perpetuation of inflammatory responses during acute peritonitis is associated with elevated peritoneal levels of cd T cells and TNF-a and detrimental clinical outcomes in infections caused by HMB-PP positive microorganisms. Taken together, our findings indicate a direct link between invading pathogens, neutrophils, monocytes and microbe-responsive cd T cells in early infection and suggest novel diagnostic and therapeutic approaches.Martin S. Davey, Chan-Yu Lin, Gareth W. Roberts, SinĂ©ad Heuston, Amanda C. Brown, James A. Chess, Mark A. Toleman, Cormac G.M. Gahan, Colin Hill, Tanya Parish, John D. Williams, Simon J. Davies, David W. Johnson, Nicholas Topley, Bernhard Moser and Matthias Eber
Human IgG1 Responses to Surface Localised Schistosoma mansoni Ly6 Family Members Drop following Praziquantel Treatment
- Author
- A Bamezai
- A Davies
- A de Morree
- A Galat
- A Garza-Garcia
- A Hijazi
- A Leaver-Fay
- A Ribeiro de Jesus
- AL Roldan
- AV Protasio
- B Eisenhaber
- B Moussian
- B Su
- BW van Balkom
- C Auriault
- CH King
- Christine Pierrot
- CM Fitzsimmons
- CM Fitzsimmons
- Colin M. Fitzsimmons
- David W. Dunne
- DG Colley
- DL Bodian
- DW Crompton
- E Hansell
- Edridah M. Tukahebwa
- EJ Farnell
- F Liu
- FA Lewis
- FC Cardoso
- FC Cardoso
- Frances M. Jones
- H Gardsvoll
- H Tallima
- Iain W. Chalmers
- IW Chalmers
- J Greenwald
- J Mulvenna
- Jakub M. Wawrzyniak
- Jamal Khalife
- JD Bendtsen
- Jeffrey Michael Bethony
- JH Chou
- JM Fitzpatrick
- K Ginalski
- Karl F. Hoffmann
- KaS W. Hofmann
- KD Pruitt
- KJ Leath
- LA de Oliveira Fraga
- LP Farias
- LP Farias
- M Berriman
- M Ismail
- M Mallya
- M Punta
- Martha Brown
- MH Meevissen
- MH Tran
- N Reimers
- Narcis Fernandez-Fuentes
- ND Young
- NR Bergquist
- R El Ridi
- RA Wilson
- RA Wilson
- RC Edgar
- S Braschi
- S Raman
- SF Altschul
- TA Wynn
- TR Hawn
- W Castro-Borges
- Publication venue
- Publication date
- 01/01/2015
- Field of study
The heptalaminate-covered, syncytial tegument is an important anatomical adaptation that enables schistosome parasites to maintain long-term, intravascular residence in definitive hosts. Investigation of the proteins present in this surface layer and the immune responses elicited by them during infection is crucial to our understanding of host/parasite interactions. Recent studies have revealed a number of novel tegumental surface proteins including three (SmCD59a, SmCD59b and Sm29) containing uPAR/Ly6 domains (renamed SmLy6A SmLy6B and SmLy6D in this study). While vaccination with SmLy6A (SmCD59a) and SmLy6D (Sm29) induces protective immunity in experimental models, human immunoglobulin responses to representative SmLy6 family members have yet to be thoroughly explored.Using a PSI-BLAST-based search, we present a comprehensive reanalysis of the Schistosoma mansoni Ly6 family (SmLy6A-K). Our examination extends the number of members to eleven (including three novel proteins) and provides strong evidence that the previously identified vaccine candidate Sm29 (renamed SmLy6D) is a unique double uPAR/Ly6 domain-containing representative. Presence of canonical cysteine residues, signal peptides and GPI-anchor sites strongly suggest that all SmLy6 proteins are cell surface-bound. To provide evidence that SmLy6 members are immunogenic in human populations, we report IgG1 (as well as IgG4 and IgE) responses against two surface-bound representatives (SmLy6A and SmLy6B) within a cohort of S. mansoni-infected Ugandan males before and after praziquantel treatment. While pre-treatment IgG1 prevalence for SmLy6A and SmLy6B differs amongst the studied population (7.4% and 25.3% of the cohort, respectively), these values are both higher than IgG1 prevalence (2.7%) for a sub-surface tegumental antigen, SmTAL1. Further, post-treatment IgG1 levels against surface-associated SmLy6A and SmLy6B significantly drop (p = 0.020 and p < 0.001, respectively) when compared to rising IgG1 levels against sub-surface SmTAL1.Collectively, these results expand the number of SmLy6 proteins found within S. mansoni and specifically demonstrate that surface-associated SmLy6A and SmLy6B elicit immunological responses during infection in endemic communities
Evidence gaps and biodiversity threats facing the marine environment of the United Kingdomâs Overseas Territories
- Author
- AB Boehm
- Adriana E. S. Ford
- AM Friedlander
- BC OâLeary
- BC OâLeary
- BC OâLeary
- Bethan C. OâLeary
- BS Halpern
- BS Halpern
- Callum M. Roberts
- CM Roberts
- Colin J. McClean
- CRC Sheppard
- CT Perry
- DA Gill
- E Shuckburgh
- GE Likens
- GJ Edgar
- GM Hilton
- J Dawson
- J Forster
- J Forster
- JE Duffy
- JL Lavers
- JP McWilliams
- JR Jambeck
- Julie P. Hawkins
- JW Readman
- K Boerder
- K Richardson
- L Gamfeldt
- L Gamfeldt
- LM Howarth
- LV Dicks
- M Amoamo
- MD Spalding
- NAJ Graham
- NC Ban
- NR Haddaway
- PB Reich
- Philip Fieldhouse
- PK Huth
- Polly Burns
- R Woesik van
- RA Watson
- RC Roche
- RT Kingsford
- S Baker
- S Diaz
- S Dâagata
- S Soliveres
- SB Weber
- SE Lester
- SM Haver
- T Churchyard
- TE Davies
- TH Oliver
- TK Davies
- TR Walker
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/02/2019
- Field of study
Understanding the evidence base and identifying threats to the marine environment is critical to ensure cost-effective management and to identify priorities for future research. The United Kingdom (UK) government is responsible for approximately 2% of the worldâs oceans, most of which belongs to its 14 Overseas Territories (UKOTs). Containing biodiversity of global significance, and far in excess of the UK mainlandâs domestic species, there has recently been a strong desire from many of the UKOTs, the UK Government, and NGOs to improve marine management in these places. Implementing evidence-based marine policy is, however, challenged by the disparate nature of scientific research in the UKOTs and knowledge gaps about the threats they face. Here, we address these issues by systematically searching for scientific literature which has examined UKOT marine biodiversity and by exploring publicly available spatial threat data. We find that UKOT marine biodiversity has received consistent, but largely low, levels of scientific interest, and there is considerable geographical and subject bias in research effort. Of particular concern is the lack of research focus on management or threats to biodiversity. The extent and intensity of threats vary amongst and within the UKOTs but unsurprisingly, climate change associated threats affect them all and direct human stressors are more prevalent in those with higher human populations. To meet global goals for effective conservation and management, there is an urgent need for additional and continued investment in research and management in the Overseas Territories, particularly those that have been of lesser focus
A Guide to Medications Inducing Salivary Gland Dysfunction, Xerostomia, and Subjective Sialorrhea: A Systematic Review Sponsored by the World Workshop on Oral Medicine VI
- Author
- A Aliko
- A Astrup
- A Bhat
- A Bouwer
- A Gordon
- A Kaya
- A Kumar
- A Mattiasson
- A Pelaez
- A Serretti
- A Villa
- A Villa
- A Vinik
- A Wolff
- A Wright
- A Wu
- AC OâConnell
- AD Garely
- AF Schatzberg
- AH Young
- AI Guerdjikova
- AJ Cutler
- AJ Gelenberg
- AJ Rothschild
- AJ Weil
- Alessandro Villa
- Alexander Ross Kerr
- AM Lynge Pedersen
- Andy Wolff
- Anne Marie Lynge Pedersen
- Ardita Aliko
- Arjan Vissink
- AW Mangel
- B Baker
- B Fulton
- B Kalis
- B Krevsky
- BA Swinburn
- BM Henz
- BN Prichard
- C Dawes
- C Delahaye
- C Katona
- C Merideth
- C Scully
- C Scully
- CA Harrington
- CE Adams
- CG Roehrborn
- CJ Halas
- CL Bowden
- CL Budman
- CM Canuso
- Colin Dawes
- CT Nguyen
- CU Pae
- D Barton
- D Devos
- D Kalman
- D Khajavi
- D Moher
- D Murdoch
- D Semel
- D Simpson
- D Smidt
- D Smidt
- D West
- DB Allison
- DE Chung
- DE Stewart
- DE Wilfley
- DGS Perahia
- DJ Hellerstein
- DJ Ossip
- DM Newnham
- Doron Aframian
- DR Staskin
- E Boven
- E Bull
- E Finlay
- E Freye
- E Johnsen
- E Karamatskos
- E Lee
- E Nagata
- E Sacco
- E Vieta
- EC Davies
- EE Lower
- EM Timpe
- EP Frakes
- F Chu
- F López-Muñoz
- F Muller
- F Riahi
- F Wang
- FL Greenway
- G Sathyan
- GD Tollefson
- GG Kay
- GG Kay
- GI Papakostas
- Gordon Proctor
- H Hashim
- H Joffe
- H Madersbacher
- H Moldofsky
- H Sauer
- HA Friedel
- HAM Kerstjens
- HP Volz
- HS Smith
- I But
- I Gilron
- I Kodish
- I Maruyama
- I Steigerwald
- J Barkin
- J Biederman
- J Biederman
- J Ekström
- J Ekström
- J Gahimer
- J Graham
- J Metello
- J Moreno
- J Webster
- JA Wilken
- JC Atkinson
- JC Blader
- JE Frampton
- JG Bova
- JG Speciali
- JG Verbalis
- JH Atkinson
- JM Monti
- JP Bennett Jr
- JP Diamond
- JP Feighner
- JP McEvoy
- JP Staab
- JP Zacny
- JR Scheepe
- JRL Schwartz
- JS Schuman
- Jörgen Ekström
- K Hewett
- K McKeage
- K Momo
- K Timdahl
- KA Tourian
- KK Kim
- KL Weihs
- KM Gadde
- KN Fountoulakis
- KS Naruganahalli
- LE Aaron
- LL Brunton
- LM Arnold
- LM Arnold
- LM Sreebny
- LM Sreebny
- M Bauer
- M Billiard
- M Coskun
- M Darwish
- M Fava
- M Jafarinia
- M Kendirci
- M Lauti
- M Pollack
- M Sakaguchi
- M Steiner
- M Tzefos
- M Versiani
- MA Katzman
- MA Soler Roibal
- MC Michel
- MC Michel
- MD Vickers
- MH Allen
- MI Wilde
- MJ Detke
- MJ Ormseth
- MJ Ormseth
- MM Koller
- MP Curran
- MR Liebowitz
- MR Semenchuk
- MR Semenchuk
- N El-Khalili
- N Zwar
- Nagamani Narayana
- NJ Carter
- NR Zinner
- O Geyer
- O Yamaguchi
- P Abrams
- P Aneja
- P Diz Dios
- P Fang
- P Gareri
- P Tutka
- P Villaseca
- PA Newhouse
- PA Zwieten van
- Pdel V Almeida de
- PM Tulkens
- PS Pawar
- PU Rani
- R Chou
- R Davis
- R Davis
- R Polosa
- RB Armstrong
- Revan Kumar Joshi
- RG Smith
- RH Weisler
- Richard McGowan
- RL Findling
- RP Malone
- RR Conley
- RS Doody
- RS McIntyre
- S Eviö
- S Herschorn
- S Kasper
- S Tramontina
- SA Montgomery
- SA Montgomery
- SG Kornstein
- SH Croog
- Siri Beier Jensen
- SJ Bajwa
- SK Praharaj
- SR Donaldson
- SR Serels
- SS Hegde
- SW Kim
- SY Fang
- T Godoy
- T Godoy
- T Godoy
- T Jain
- T Nederfors
- T Oki
- T Seo
- T Suppes
- T Wigal
- TA Pigott
- TE Brown
- TL Griebling
- TO Narhi
- TR Norman
- TR Walters
- U Jonas
- V Gerc
- V Immadisetty
- V Khullar
- V PlÀnitz
- VL Ellingrod
- VL Stauffer
- VR Lucente
- VW Nitti
- W Aberer
- W Lasheen
- W Vongpatanasin
- WA Hening
- WA James
- WW Storms
- Y Homma
- Y Homma
- Y Oba
- Ying Wai Sia
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Recommended from our members
Search for new Higgs bosons via same-sign top quark pair production in association with a jet in proton-proton collisions at âs = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbott S
- Abbrescia M
- Abdalla H
- Abdullin S
- Abreu A
- Abu Zeid S
- Acharya H
- Acharya S
- Acosta D
- Adam W
- Adamidis K
- Adams MR
- Adams T
- Addesa FM
- Adloff C
- Adzic P
- Aebi D
- Afanasiev S
- Agapitos A
- Agarwal G
- Agram J-L
- Aguilar-Benitez M
- Agyel D
- Ahmad A
- Ahmad M
- Ahmed A
- AimĂš C
- Ajmal S
- Akchurin N
- Akgun B
- Akpinar A
- Al Kadhim A
- Albert A
- Albrecht A
- Albrecht S
- Albrow M
- Alcaraz Maestre J
- Alcerro Alcerro LF
- Aldaya Martin M
- AldĂĄ JĂșnior WL
- Aleksandrov A
- Alexander J
- Alhusseini M
- Alimena J
- Alison J
- Allmond B
- Ally D
- Almond J
- Alpana A
- Alsufyani B
- Alvarez Gonzalez B
- Alverson G
- Alves Gallo Pereira M
- Alves GA
- Aly R
- Alyari M
- Amapane N
- Ambrozas M
- Ameen MM
- Amendola C
- Amoroso S
- Amram O
- Amsler C
- An S
- An Y
- Anagnostou G
- Andrea J
- Andreev V
- Andreev Y
- Andrejkovic JW
- Andrews MB
- Androsov K
- Anguiano J
- Antchev G
- Anthony D
- Antonello M
- Apollinari G
- Apparu D
- Appelt E
- Apresyan A
- Araujo M
- Aravind A
- Arcaro D
- Arcidiacono R
- Ardino R
- Argiro S
- Arneodo M
- Aruta C
- Asawatangtrakuldee C
- Asenov P
- Asghar MI
- Asilar E
- Askew A
- Assiouras P
- Assran Y
- Atakisi IO
- Attikis A
- Auffray E
- Aushev T
- Auzinger G
- Avati V
- Avery P
- Avila C
- Awais A
- Awan MIM
- Ayala E
- Ayala G
- Aydilek O
- Azarkin M
- Azzi P
- Azzurri P
- Baarmand MM
- Babaev A
- Babbar J
- Bacchetta N
- Bachtis M
- Backhaus M
- Baden A
- Baechler J
- Bagliesi G
- Bahinipati S
- Bainbridge R
- Bak G
- Bakas G
- Bakhshiansohi H
- Bakshi AS
- Bala A
- Baldenegro Barrera C
- Ball AH
- Bam B
- Ban Y
- Band R
- Bandyopadhyay H
- Banerjee S
- Banerjee S
- Bansal S
- Baradia S
- Barbagli G
- Barberis E
- Barbosa Trujillo DA
- Bardelli G
- Bargassa P
- Baringer P
- Barman S
- Barnes VE
- Barney D
- Barria P
- Barroso Ferreira Filho M
- Bartek R
- Bartosik N
- BartĂłk M
- Barzdukas A
- Basnet A
- Bastos D
- Battilana C
- Baty A
- Bauer G
- Bauerdick LAT
- Bautista I
- Baxter S
- Bayatmakou M
- Bean A
- Beauceron S
- Beaudette F
- Becerril Gonzalez H
- Bedoya CF
- Behera PK
- Behera SC
- Behnke O
- Bein S
- BeirĂŁo Da Cruz E Silva C
- Belforte S
- Bell KW
- Bellan R
- Belloni A
- Bellora A
- Belvedere A
- Belyaev A
- Belyaev A
- Benaglia A
- Benato L
- Bencze G
- Bendavid J
- Benecke A
- Benelli G
- Benitez JF
- Bennett C
- Benussi L
- Bergauer T
- Beri SB
- BermĂșdez MartĂnez A
- Bernardes CA
- Berry D
- Berryhill J
- Besancon M
- Bestintzanos I
- Bethani A
- Bevilacqua T
- Beyrouthy T
- Bhardwaj A
- Bharthuar S
- Bhat PC
- Bhatnagar V
- Bhattacharya R
- Bhattacharya S
- Bhattacharya S
- Bhattacharya S
- Bhowmik D
- Bhowmik S
- Bhyun JH
- Bialkowska H
- Bianchini L
- Bianco M
- Bianco S
- Biino C
- Bilei GM
- Bilin B
- Bin Anuar AA
- Bin Norjoharuddeen N
- Bisello D
- Black K
- Blanco FernĂĄndez S
- Blancon B
- Blekman F
- Blend D
- Blinov V
- Bloch D
- Bloch P
- Bloom K
- Bluj M
- Blumenfeld B
- Boccali T
- Bocci A
- Bodek A
- Boimska B
- Boldrini G
- Boletti A
- Bols ES
- Bonacorsi D
- Bonanomi M
- Bonilla J
- Boos E
- Boran F
- Borgonovi L
- Bornheim A
- Borras K
- Borshch V
- Bortignon P
- Bose T
- Bossini E
- Botta C
- Botta V
- Bouchamaoui H
- Boudoul G
- Bouhali O
- Bourilkov D
- Bower N
- Boyaryntsev A
- Bozzo M
- Bragagnolo A
- Braghieri A
- Brainerd C
- Brandao Malbouisson H
- Branson JG
- Breedon R
- Brennan L
- Brew C
- Bright-Thonney S
- Brigljevic V
- Brinkerhoff A
- Brivio F
- Brochero Cifuentes JA
- Brom J-M
- Brommer S
- Brondolin E
- Brooke JJ
- Brown CE
- Brown RM
- Brunner D
- Bruno G
- Bruschini D
- Bryant P
- Bryson M
- Brzhechko D
- BrĂŒcken E
- Bubanja I
- Bucci R
- Buchmuller O
- Buchot Perraguin A
- Budkouski D
- Bueghly J
- Bundock A
- Bunichev V
- Bunkowski K
- Buontempo S
- Burkart M
- Burkett K
- Bury F
- Busson P
- Busza W
- Butalla S
- Butler JN
- Butler PH
- Butz E
- Bylsma B
- BĂ€rtschi P
- Cabrera A
- Cabrillo IJ
- Cacchio V
- Cadamuro L
- Cagnotta A
- Caillol C
- Cakir A
- Calandri A
- Calderon De La Barca Sanchez M
- Calderon A
- Cali IA
- Calligaris L
- Calzaferri S
- Camaiani B
- Caminada L
- Campagnari C
- Campana M
- Campanini R
- Campbell A
- Camporesi T
- Candelise V
- Canelli MF
- Canepa A
- Cankocak K
- Capiluppi P
- Cappati A
- Caputo C
- Caraway B
- Cardini A
- Cardwell B
- Carlin R
- Carnahan T
- Carnevali F
- Carrera Jarrin E
- Carrigan M
- Carrillo Montoya CA
- Cartiglia N
- Carvalho W
- Casarsa M
- Cassese A
- Castaldi R
- Castaneda Hernandez A
- Castells S
- Castilla-Valdez H
- Castro A
- Cavallari F
- Cavallo FR
- Cavallo N
- Cavanaugh R
- Cazzaniga C
- Ceard L
- Ceccarelli R
- Cepeda M
- Cerati GB
- Cerci S
- Cerminara G
- Cerrada M
- Cerri O
- Cetorelli F
- Chabert EC
- Chahal GS
- Chandra S
- Chang P
- Chanon N
- Chao Y
- Charlot C
- Chatagnon P
- Chatterjee RM
- Chatterjee S
- Chatterjee S
- Chatzistavrou T
- Chaudhary G
- Chauhan S
- Chawla R
- Checchia P
- Chekhovsky V
- Chen GM
- Chen HS
- Chen KF
- Chen M
- Chen PS
- Chen X
- Chen Y
- Chen YM
- Chen Z
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- Yuldashev BS
- Yusuff I
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- Zuolo D
- Zygala L
- Publication venue
- Elsevier
- Publication date
- 02/02/2024
- Field of study
Data availability:
Release and preservation of data used by the CMS Collaboration as the basis for publications is guided by the CMS policy as stated in âCMS data preservation, re-use and open access policyâ available online at: https://cms-docdb.cern.ch/cgi-bin/PublicDocDB/RetrieveFile?docid=6032&filename=CMSDataPolicyV1.2.pdf&version=2 .A preprint of this article is available online at arXiv:2311.03261v2 [hep-ex] https://arxiv.org/abs/2311.03261v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/TOP-22-010 (CMS Public Pages)A search is presented for new Higgs bosons in proton-proton (pp) collision events in which a same-sign top quark pair is produced in association with a jet, via the pp â tH/A â ttÂŻc and pp â tH/A â ttÂŻu processes. Here, H and A represent the extra scalar and pseudoscalar boson, respectively, of the second Higgs doublet in the generalized two-Higgs-doublet model (g2HDM). The search is based on pp collision data collected at a center-of-mass energy of 13 TeV with the CMS detector at the LHC, corresponding to an integrated luminosity of 138 fbâ1. Final states with a same-sign lepton pair in association with jets and missing transverse momentum are considered. New Higgs bosons in the 200-1000 GeV mass range and new Yukawa couplings between 0.1 and 1.0 are targeted in the search, for scenarios in which either H or A appear alone, or in which they coexist and interfere. No significant excess above the standard model prediction is observed. Exclusion limits are derived in the context of the g2HDM.SCOAP3
Recommended from our members
Measurement of the Higgs boson production via vector boson fusion and its decay into bottom quarks in proton-proton collisions at sâ = 13 TeV
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- Aarup Petersen H
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- Publication venue
- Springer Nature on behalf of SISSA
- Publication date
- 30/01/2024
- Field of study
A preprint version of the article is available at arXiv:2308.01253v2 [hep-ex], https://arxiv.org/abs/2308.01253v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/HIG-22-009 (CMS Public Pages). Report number: CMS-HIG-22-009, CERN-EP-2023-110.A measurement of the Higgs boson (H) production via vector boson fusion (VBF) and its decay into a bottom quark-antiquark pair (bbÂŻ) is presented using proton-proton collision data recorded by the CMS experiment at sâ = 13 TeV and corresponding to an integrated luminosity of 90.8 fbâ1. Treating the gluon-gluon fusion process as a background and constraining its rate to the value expected in the standard model (SM) within uncertainties, the signal strength of the VBF process, defined as the ratio of the observed signal rate to that predicted by the SM, is measured to be ÎŒqqHHbbÂŻ = 1.01 +0.55â0.46. The VBF signal is observed with a significance of 2.4 standard deviations relative to the background prediction, while the expected significance is 2.7 standard deviations. Considering inclusive Higgs boson production and decay into bottom quarks, the signal strength is measured to be ÎŒincl.HbbÂŻ = 0.99 +0.48â0.41, corresponding to an observed (expected) significance of 2.6 (2.9) standard deviations.SCOAP3, STFC; Marie-Curie program and the European Research Council and Horizon 2020 Gran
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Search for direct production of GeV-scale resonances decaying to a pair of muons in proton-proton collisions at sâ = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbott S
- Abbrescia M
- Abdullah Al-Mashad M
- Abdullin S
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- Publication venue
- Springer Nature on behalf of SISSA
- Publication date
- 30/11/2023
- Field of study
A preprint version of the article is available at arXiv:2309.16003v2 [hep-ex], https://arxiv.org/abs/2309.16003v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables, including additional supplementary figures, can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/EXO-21-005 (CMS Public Pages). Report number: CMS-EXO-21-005, CERN-EP-2023-165.A search for direct production of low-mass dimuon resonances is performed using sâ = 13 TeV proton-proton collision data collected by the CMS experiment during the 2017-2018 operation of the CERN LHC with an integrated luminosity of 96.6 fbâ1. The search exploits a dedicated high-rate trigger stream that records events with two muons with transverse momenta as low as 3 GeV but does not include the full event information. The search is performed by looking for narrow peaks in the dimuon mass spectrum in the ranges of 1.1-2.6 GeV and 4.2-7.9 GeV. No significant excess of events above the expectation from the standard model background is observed. Model-independent limits on production rates of dimuon resonances within the experimental fiducial acceptance are set. Competitive or world's best limits are set at 90% confidence level for a minimal dark photon model and for a scenario with two Higgs doublets and an extra complex scalar singlet (2HDM+S). Values of the squared kinetic mixing coefficient Δ2 in the dark photon model above 10â6 are excluded over most of the mass range of the search. In the 2HDM+S, values of the mixing angle sin(ΞH) above 0.08 are excluded over most of the mass range of the search with a fixed ratio of the Higgs doublets vacuum expectation tanÎČ = 0.5.SCOAP3
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Search for WâČ bosons decaying to a top and a bottom quark in leptonic final states in proton-proton collisions at sâ = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
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- Abbrescia M
- Abdullah Al-Mashad M
- Abdullin S
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- Abu Zeid S
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- Aebi D
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- Alcerro Alcerro LF
- Aldaya Martin M
- AldĂĄ JĂșnior WL
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- Publication venue
- Springer Nature
- Publication date
- 05/04/2024
- Field of study
A preprint version of the article is available at arXiv:2310.19893v1 [hep-ex], https://arxiv.org/abs/2310.19893v1 . Comments: Submitted to the Journal of High Energy Physics. All figures and tables can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/B2G-20-012 (CMS Public Pages). Report number: CMS-B2G-20-012, CERN-EP-2023-213.A search for W' bosons decaying to a top and a bottom quark in final states including an electron or a muon is performed with the CMS detector at the LHC. The analyzed data correspond to an integrated luminosity of 138 fb^{-1} of proton-proton collisions at a center-of-mass energy of 13 Tev. Good agreement with the standard model expectation is observed and no evidence for the existence of the W' boson is found over the mass range examined. The largest observed deviation from the standard model expectation is found for a W' boson mass (mWâČ) hypothesis of 3.8 TeV with a relative decay width of 1%, with a local (global) significance of 2.6 (2.0) standard deviations. Upper limits on the production cross sections of W' bosons decaying to a top and a bottom quark are set. Left- and right-handed W' bosons with mWâČ below 3.9 and 4.3 TeV, respectively, are excluded at the 95% confidence level, under the assumption that the new particle has a narrow decay width. Limits are also set for relative decay widths up to 30%. These are the most stringent limits to date on this W' boson decay channel.SCOAP3
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- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
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- Abbrescia M
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- Publication venue
- Springer Nature on behalf of SISSA
- Publication date
- 19/03/2024
- Field of study
A preprint version of the article is available at arXiv:2312.07484v3 [hep-ex], https://arxiv.org/abs/2312.07484 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/EXO-21-013 (CMS Public Pages)A search for long-lived heavy neutral leptons (HNLs) is presented, which considers the hadronic final state and coupling scenarios involving all three lepton generations in the 2-20 GeV HNL mass range for the first time. Events comprising two leptons (electrons or muons) and jets are analyzed in a data sample of proton-proton collisions, recorded with the CMS experiment at the CERN LHC at a centre-of-mass energy of 13 TeV, corresponding to an integrated luminosity of 138 fbâ1. A novel jet tagger, based on a deep neural network, has been developed to identify jets from an HNL decay using various features of the jet and its constituent particles. The network output can be used as a powerful discriminating tool to probe a broad range of HNL lifetimes and masses. Contributions from background processes are determined from data. No excess of events in data over the expected background is observed. Upper limits on the HNL production cross section are derived as functions of the HNL mass and the three coupling strengths VâN to each lepton generation â and presented as exclusion limits in the coupling-mass plane, as lower limits on the HNL lifetime, and on the HNL mass. In this search, the most stringent limit on the coupling strength is obtained for pure muon coupling scenarios; values of |VÎŒN|2 > 5 (4) Ă 10â7 are excluded for Dirac (Majorana) HNLs with a mass of 10 GeV at a confidence level of 95% that correspond to proper decay lengths of 17 (10) mm.SCOAP3