Bruce Cree

ORCID: 0000-0001-7689-2533
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About
Contact & Profiles
Research Areas
  • Multiple Sclerosis Research Studies
  • Peripheral Neuropathies and Disorders
  • Polyomavirus and related diseases
  • Systemic Lupus Erythematosus Research
  • Sphingolipid Metabolism and Signaling
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • Rheumatoid Arthritis Research and Therapies
  • Monoclonal and Polyclonal Antibodies Research
  • Systemic Sclerosis and Related Diseases
  • Autoimmune and Inflammatory Disorders Research
  • Cytokine Signaling Pathways and Interactions
  • Acute Lymphoblastic Leukemia research
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Viral Infections and Immunology Research
  • Gut microbiota and health
  • Fungal Infections and Studies
  • Phytochemistry and Biological Activities
  • Liver Diseases and Immunity
  • RNA regulation and disease
  • Neuroinflammation and Neurodegeneration Mechanisms
  • SARS-CoV-2 and COVID-19 Research
  • Research on Leishmaniasis Studies
  • Chronic Lymphocytic Leukemia Research
  • Fungal Plant Pathogen Control

University of California, San Francisco
2016-2025

University of Basel
2021-2024

University of Pennsylvania
2018-2024

Center for Neurosciences
2020-2024

Heinrich Heine University Düsseldorf
2010-2024

St. Josef-Hospital
2014-2024

University of Nevada, Reno
2024

Renown Health
2024

Johns Hopkins University
2018-2024

Ruhr University Bochum
2014-2024

Stephen Sawcer Garrett Hellenthal Matti Pirinen Chris C. A. Spencer Nikolaos A. Patsopoulos and 95 more Loukas Moutsianas Alexander Dilthey Zhan Su Colin Freeman Sarah Hunt Sarah Edkins Emma Gray David R. Booth Simon Potter An Goris Gavin Band Annette Oturai Amy Strange Janna Saarela Céline Bellenguez Bertrand Fontaine Matthew Gillman Bernhard Hemmer Rhian Gwilliam Frauke Zipp Alagurevathi Jayakumar Roland Martinꝉ Stephen Leslie Stanley Hawkins Eleni Giannoulatou Sandra D’Alfonso Hannah Blackburn Filippo Martinelli Boneschi Jennifer Liddle Hanne F. Harbo M. L. Perez Anne Spurkland Matthew Waller Marcin P. Mycko Michelle Ricketts Manuel Comabella Naomi Hammond Ingrid Kockum Owen T McCann Maria Ban Pamela Whittaker Anu Kemppinen Paul A. Weston Clive Hawkins Sara Widaa John Zajicek Serge Dronov Neil P. Robertson Suzannah J. Bumpstead Lisa F. Barcellos Rathi Ravindrarajah Roby Abraham Lars Alfredsson Kristin Ardlie Cristin Aubin Amie Baker K. Baker Sergio E. Baranzini Laura Bergamaschi Roberto Bergamaschi Allan Bernstein Achim Berthele Mike Boggild Jonathan P. Bradfield David Brassat Simon Broadley Dorothea Buck Helmut Butzkueven Ruggero Capra William M. Carroll Paola Cavalla Elisabeth Gulowsen Celius Sabine Cepok Rosetta Chiavacci Françoise Clerget‐Darpoux Katleen Clysters Gıancarlo Comı M. Cossburn Isabelle Cournu‐Rebeix Mathew Cox Wendy Cozen Bruce Cree Anne H. Cross Daniele Cusi Mark J. Daly Emma Davis Paul I. W. de Bakker Marc Debouverie Marie D’hooghe Katherine Dixon Rita Dobosi Bénédicte Dubois David Ellinghaus Irina Elovaara Federica Esposito

10.1038/nature10251 article EN Nature 2011-08-01

Multiple sclerosis has a clinically significant heritable component. We conducted genomewide association study to identify alleles associated with the risk of multiple sclerosis.We used DNA microarray technology common sequence variants in 931 family trios (consisting an affected child and both parents) tested them for association. For replication, we genotyped another 609 trios, 2322 case subjects, 789 control subjects genotyping data from two external sets. A joint analysis 12,360 was...

10.1056/nejmoa073493 article EN New England Journal of Medicine 2007-07-30
Ashley Beecham Nikolaos A. Patsopoulos Dionysia K. Xifara Mary F. Davis Anu Kemppinen and 95 more Chris Cotsapas Tejas Shah Chris C. A. Spencer David J. Booth An Goris Annette Oturai Janna Saarela Bertrand Fontaine Bernhard Hemmer Claes Martin Frauke Zipp Sandra D’Alfonso Filippo Martinelli Boneschi Bruce Taylor Hanne F. Harbo Ingrid Kockum Jan Hillert Tomas Olsson Maria Ban Jorge R. Oksenberg Rogier Hintzen Lisa F. Barcellos Cristina Agliardi Lars Alfredsson Mehdi Alizadeh Carl A. Anderson Robert Andrews Helle Bach Søndergaard Amie Baker Gavin Band Sergio E. Baranzini Nadia Barizzone Jeffrey C. Barrett Céline Bellenguez Laura Bergamaschi Luisa Bernardinelli Achim Berthele Viola Biberacher Thomas M.C. Binder Hannah Blackburn Izaura Lima Bomfim Paola Brambilla Simon Broadley Bruno Brochet Lou Brundin Dorothea Buck Helmut Butzkueven Stacy J. Caillier William Camu Wassila Carpentier Paola Cavalla Elisabeth Gulowsen Celius Irène Coman Gıancarlo Comı Lucia Corrado Leentje Cosemans Isabelle Cournu‐Rebeix Bruce Cree Daniele Cusi Vincent Damotte Gilles Defer Silvia Delgado Panos Deloukas Alessia Di Sapio Alexander Dilthey Peter Donnelly Bénédicte Dubois Martin Duddy Sarah Edkins Irina Elovaara Federica Esposito Nikos Evangelou Barnaby Fiddes Judith Field André Franke Colin Freeman Irene Y. Frohlich Daniela Galimberti Christian Gieger Pierre‐Antoine Gourraud Christiane Graetz Andrew Graham Verena Grummel Clara Guaschino Athena Hadjixenofontos Hákon Hákonarson Christopher Halfpenny Gillian Hall Per Hall Anders Hamsten James Harley Timothy Harrower Clive Hawkins Garrett Hellenthal Charles Hillier

10.1038/ng.2770 article EN Nature Genetics 2013-09-29

Significance We have experimentally investigated the immunoregulatory effects of human gut microbiota in multiple sclerosis (MS). identified specific bacteria that are associated with MS and demonstrated these regulate T lymphocyte-mediated adaptive immune responses contribute to proinflammatory environment vitro vivo. Thus, our results expand knowledge microbial regulation immunity may provide a basis for development microbiome-based therapeutics autoimmune diseases.

10.1073/pnas.1711235114 article EN Proceedings of the National Academy of Sciences 2017-09-11
Ludwig Kappos Amit Bar‐Or Bruce Cree Robert J. Fox Gavin Giovannoni and 95 more Ralf Gold Patrick Vermersch Douglas L. Arnold Sophie Arnould Tatiana Scherz Christian Wolf Erik Wallström Frank Dahlke Anat Achiron Lutz Achtnichts Kadriye Ağan Gülşen Akman‐Demir Alison Allen Jack P. Antel Alfredo Rodríguez Antigüedad Michelle Apperson Angela Applebee Guillermo Izquierdo Ayuso Masayuki Baba Ovidiu Båjenaru Rodica Balasa Belgin Petek Balcı Michael Barnett Ann Bass V. Becker Mihaela Bejinariu Florian Then Bergh Arnfin Bergmann Evanthia Bernitsas Achim Berthele Virender Bhan Felix Bischof Randall J. Bjork Gregg Blevins Matthias Boehringer Thomas Boerner Robert Bonek James D. Bowen Allen C. Bowling Alexey Boyко Cavit Boz Vera Bracknies Stefan Braune Vincenzo Brescia Morra Bruno Brochet Waldemar Brola Paul Brownstone M Brozman Donald Brunet Ioan Buraga Margaret Burnett Mathias Buttmann Helmut Butzkueven Jonathan Cahill Jonathan Calkwood William Camu Mark Cascione G. Castelnovo Diego Centonze João Cerqueira Andrew Chan Andrea Cimprichová Stanley Cohan Giancarlo Comi Jill Ker Conway Joanna Cooper John R. Corboy Jorge Correale Brian Costell David A. Cottrell Patricia K. Coyle Matthew Craner Liying Cui Luı́s Cunha Anna Członkowska Ana Martins da Silva Joao de de Sèze Marc Debouverie Jan Debruyne D. Decoo G. Defer Tobias Derfuß Norma Deri Bhupesh Dihenia Péter Diószeghy Vladimír Donáth Bénédicte Dubois Martin Duddy Pierre Duquette Gilles Edan Hüsnü Efendi Stanton B. Elias Peter Emrich Bonaventura Casanova Estruch

10.1016/s0140-6736(18)30475-6 article EN The Lancet 2018-03-01

Eight patients with worsening neuromyelitis optica were treated rituximab to achieve B cell depletion. Treatment was well tolerated. Six of eight relapse free and median attack rate declined from 2.6 attacks/patient/year 0 (<i>p</i> = 0.0078). Seven experienced substantial recovery neurologic function over 1 year average follow-up. The pretreatment Expanded Disability Status Scale score 7.5, at follow-up examination 5.5 0.013).

10.1212/01.wnl.0000159399.81861.d5 article EN Neurology 2005-04-12

Objective To develop recommendations for disease-modifying therapy (DMT) multiple sclerosis (MS). Methods A multidisciplinary panel developed DMT recommendations, integrating findings from a systematic review; followed an Institute of Medicine–compliant process to ensure transparency and patient engagement; modified Delphi consensus–based concerning starting, switching, stopping DMTs pertinent people with relapsing-remitting MS, secondary progressive primary clinically isolated syndromes...

10.1212/wnl.0000000000005347 article EN Neurology 2018-04-23

Multiple sclerosis (MS), a chronic disorder of the central nervous system and common cause neurological disability in young adults, is characterized by moderate but complex risk heritability. Here we report results genome-wide association study performed 1000 prospective case series well-characterized individuals with MS group-matched controls using Sentrix® HumanHap550 BeadChip platform from Illumina. After stringent quality control data filtering, compared allele frequencies for 551 642...

10.1093/hmg/ddn388 article EN Human Molecular Genetics 2008-11-14

Neuromyelitis optica (NMO) is an uncommon, life-threatening inflammatory demyelinating disorder. Recently, much has become known about its immunopathogenesis. However, optimal treatments, with expected outcomes, have not been established.To evaluate the use and efficacy of rituximab for treating NMO.Retrospective multicenter case series NMO patients treated rituximab.Seven tertiary medical centers in United States England.Twenty-five (including 2 children), 23 whom experienced relapses...

10.1001/archneur.65.11.noc80069 article EN Archives of Neurology 2008-09-09

To characterize the accrual of long-term disability in a cohort actively treated multiple sclerosis (MS) patients and to assess whether clinical magnetic resonance imaging (MRI) data used trials have prognostic value.This is prospective study 517 managed MS enrolled at single center.More than 91% were retained, with ascertained up 10 years after baseline visit. At this last assessment, neurologic as measured by Expanded Disability Status Scale (EDSS) was stable or improved compared 41%...

10.1002/ana.24747 article EN cc-by-nc-nd Annals of Neurology 2016-07-27

Objective Rates of worsening and evolution to secondary progressive multiple sclerosis (MS) may be substantially lower in actively treated patients compared natural history studies from the pretreatment era. Nonetheless, our recently reported prospective cohort, more than half with relapsing MS accumulated significant new disability by 10th year follow‐up. Notably, “no evidence disease activity” at 2 years did not predict long‐term stability. Here, we determined what extent clinical relapses...

10.1002/ana.25463 article EN cc-by-nc Annals of Neurology 2019-03-09

Abstract Objective: Aquaporin 4 (AQP4)‐specific autoantibodies in neuromyelitis optica (NMO) are immunoglobulin (Ig)G1, a T cell‐dependent Ig subclass, indicating that AQP4‐specific cells participate NMO pathogenesis. Our goal was to identify and characterize patients healthy controls (HC). Methods: Peripheral blood from HC were examined for recognition of AQP4 production proinflammatory cytokines. Monocytes evaluated cell‐polarizing cytokines expression costimulatory molecules. Results:...

10.1002/ana.23651 article EN other-oa Annals of Neurology 2012-05-25

Significance Dimethyl fumarate (DMF) (BG-12, Tecfidera), a fumaric acid ester (FAE), is commonly prescribed oral therapy for multiple sclerosis (MS), CNS autoimmune inflammatory demyelinating disease that may result in sustained neurologic damage. It thought the benefit of DMF MS mediated through activation antioxidative transcription factor nuclear (erythroid-derived 2)-like 2 (Nrf2) pathway. However, role Nrf2 antiinflammatory effects has not been fully elucidated. Here, we investigated...

10.1073/pnas.1603907113 article EN Proceedings of the National Academy of Sciences 2016-04-13

Background: ‘No evidence of disease activity’ (NEDA), defined as absence magnetic resonance imaging activity (T2 and/or gadolinium-enhanced T1 lesions), relapses and disability progression (‘NEDA-3’), is used a comprehensive measure treatment response in relapsing multiple sclerosis (RMS), but weighted towards inflammatory activity. Accelerated brain volume loss (BVL) occurs RMS an objective worsening progression. Objective: To assess the contribution individual components NEDA-3 impact...

10.1177/1352458515616701 article EN cc-by-nc Multiple Sclerosis Journal 2016-01-11

<h3>Background:</h3> Technological advancements in neuroimaging and the increased use of these diagnostic modalities are responsible for discovery incidentally identified anomalies within CNS. In addition to identification unanticipated brain MRI abnormalities suggestive demyelinating disease patients undergoing a medical reason other than evaluation multiple sclerosis (MS), asymptomatic spinal cord lesions periodically identified. <h3>Objective:</h3> To determine if associated with clinical...

10.1212/wnl.0b013e31820d8b1d article EN Neurology 2011-01-27

In multiple sclerosis (MS) pathogenic B cells likely act on both sides of the blood-brain barrier (BBB). However, it is unclear whether antigen-experienced are shared between CNS and peripheral blood (PB) compartments. We applied deep repertoire sequencing IgG heavy chain variable region genes (IgG-VH) in paired cerebrospinal fluid PB samples from patients with MS other neurological diseases to identify related that common For first time our knowledge, we found a restricted pool clonally...

10.1172/jci63842 article EN Journal of Clinical Investigation 2012-11-19
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