Jens Kühle

ORCID: 0000-0002-6963-8892
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About
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Research Areas
  • Multiple Sclerosis Research Studies
  • Amyotrophic Lateral Sclerosis Research
  • Skin and Cellular Biology Research
  • Polyomavirus and related diseases
  • Peripheral Neuropathies and Disorders
  • Parkinson's Disease Mechanisms and Treatments
  • Neuroinflammation and Neurodegeneration Mechanisms
  • RNA regulation and disease
  • Rheumatoid Arthritis Research and Therapies
  • Advanced Neuroimaging Techniques and Applications
  • Neurogenesis and neuroplasticity mechanisms
  • Alzheimer's disease research and treatments
  • Prion Diseases and Protein Misfolding
  • Hereditary Neurological Disorders
  • Systemic Sclerosis and Related Diseases
  • Long-Term Effects of COVID-19
  • Neurogenetic and Muscular Disorders Research
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Immunotherapy and Immune Responses
  • S100 Proteins and Annexins
  • Autoimmune and Inflammatory Disorders Research
  • Systemic Lupus Erythematosus Research
  • Acute Lymphoblastic Leukemia research
  • Mycobacterium research and diagnosis
  • Monoclonal and Polyclonal Antibodies Research

University Hospital of Basel
2016-2025

University of Basel
2015-2025

University Medical Center Freiburg
2011-2025

University of Freiburg
2008-2024

Hospital Base
2008-2024

University College London
2009-2024

Institute of Neuroimmunology of the Slovak Academy of Sciences
2017-2024

Institute for Biomedicine
2024

Neurology, Inc
2002-2024

The University of Melbourne
2020-2023

Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system unknown etiology. We tested hypothesis that MS caused by Epstein-Barr virus (EBV) in cohort comprising more than 10 million young adults on active duty US military, 955 whom were diagnosed with during their period service. Risk increased 32-fold after infection EBV but was not other viruses, including similarly transmitted cytomegalovirus. Serum levels neurofilament light chain, biomarker...

10.1126/science.abj8222 article EN other-oa Science 2022-01-14

Neurofilament light chains (NfL) are unique to neuronal cells, shed the cerebrospinal fluid (CSF), and detectable at low concentrations in peripheral blood. Various diseases causing damage have resulted elevated CSF concentrations. We explored value of an ultrasensitive single-molecule array (Simoa) serum NfL (sNfL) assay multiple sclerosis (MS).sNfL levels were measured healthy controls (HC, n = 254) two independent MS cohorts: (1) cross-sectional with paired samples (n 142), (2)...

10.1002/ana.24954 article EN cc-by-nc-nd Annals of Neurology 2017-05-17

There is a long history of research into body fluid biomarkers in neurodegenerative and neuroinflammatory diseases. However, only few CSF are being used clinical practice. One the most critical factors biomarker inadequate powering studies because lack sufficient samples that can be obtained single-center studies. Therefore, collaboration between investigators needed to establish large biobanks well-defined samples. Standardized protocols for biobanking prerequisite ensure statistical power...

10.1212/wnl.0b013e3181c47cc2 article EN Neurology 2009-11-30

Abstract Background: Neuronal damage is the morphological substrate of persisting neurological disability. Neurofilaments (Nf) are specific cytoskeletal proteins neurons and their quantification has shown encouraging results as a biomarker for axonal injury. Methods: We aimed at comparing widely used conventional ELISA Nf light chain (NfL) with an electrochemiluminescence-based method (ECL assay) newly developed single-molecule array (Simoa) in clinically relevant cerebrospinal fluid (CSF)...

10.1515/cclm-2015-1195 article EN Clinical Chemistry and Laboratory Medicine (CCLM) 2016-04-12

Neurofilament light protein (NfL) is elevated in cerebrospinal fluid (CSF) of a number neurological conditions compared with healthy controls (HC) and candidate biomarker for neuroaxonal damage. The influence age sex largely unknown, levels across disorders have not been systematically to date.

10.1001/jamaneurol.2019.1534 article EN JAMA Neurology 2019-06-17

To test blood and CSF neurofilament light chain (NfL) levels in relation to disease progression survival amyotrophic lateral sclerosis (ALS).

10.1212/wnl.0000000000001642 article EN cc-by Neurology 2015-05-02

Abstract Neurofilament light (NfL) protein is a marker of neuro-axonal damage and can be measured not only in cerebrospinal fluid but also serum, which allows for repeated assessments. There still limited knowledge regarding the association serum NfL (sNfL) with age subclinical morphologic brain changes their dynamics normal population. We sNfL by single molecule array (Simoa) assay 335 individuals participating population-based cohort study after mean follow-up time 5.9 years (n = 103)....

10.1038/s41467-020-14612-6 article EN cc-by Nature Communications 2020-02-10

ObjectiveNeuronal damage is the morphological substrate of persisting neurological disability. Neurofilaments (Nf) are cytoskeletal proteins neurons and their release into cerebrospinal fluid has shown encouraging results as a biomarker for neurodegeneration. This study aimed to validate quantification Nf light chain (NfL) in blood samples, biofluid source easily accessible longitudinal studies. MethodsWe developed applied highly sensitive electrochemiluminescence (ECL) based immunoassay NfL...

10.1371/journal.pone.0075091 article EN cc-by PLoS ONE 2013-09-20

<h3>Objective</h3> To assess the value of blood neurofilament light chain (NfL) as a biomarker recent, ongoing, and future disease activity tissue damage its utility to monitor treatment response in relapsing-remitting multiple sclerosis. <h3>Methods</h3> We measured NfL samples from 589 patients with sclerosis (from phase 3 studies fingolimod vs placebo, FREEDOMS interferon [IFN]-β-1a, TRANSFORMS) 35 healthy controls compared levels clinical MRI-related outcomes. <h3>Results</h3> At...

10.1212/wnl.0000000000007032 article EN cc-by-nc-nd Neurology 2019-02-09

Neuro-axonal injury is a key factor in the development of permanent disability multiple sclerosis. Neurofilament light chain peripheral blood has recently emerged as biofluid marker reflecting neuro-axonal damage this disease. We aimed at comparing serum neurofilament levels sclerosis and healthy controls, to determine their association with measures disease activity ability predict future clinical worsening well brain spinal cord volume loss. was measured by single molecule array assay 2183...

10.1093/brain/awy154 article EN Brain 2018-05-13

The oral immunomodulator FTY720 has shown efficacy in patients with relapsing multiple sclerosis (MS). functionally antagonizes sphingosine 1-phosphate receptor-1 (S1P1) on T cells and consequently inhibits S1P/S1P1-dependent lymphocyte egress from secondary lymphoid organs. Little is known about the phenotype function of remaining peripheral blood during long-term treatment.T FTY720-treated, interferon-beta (IFNbeta)-treated untreated MS, healthy donors (HD) were analyzed respect to cell...

10.1212/01.wnl.0000327609.57688.ea article EN Neurology 2008-10-13

Cerebrospinal fluid collection by lumbar puncture (LP) is performed in the diagnostic workup of several neurological brain diseases. Reluctance to perform procedure among others due a lack standards and guidelines minimize risk complications, such as post-LP headache or back pain.We provide consensus for LP complications. The recommendations are based on (1) data from large multicenter feasibility study (evidence level II-2), (2) systematic literature review needle characteristics...

10.1016/j.dadm.2017.04.007 article EN cc-by-nc-nd Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring 2017-01-01
Jens Kühle Giulio Disanto Ruth Dobson Rocco Adiutori Luca Bianchi and 94 more J. Topping JP. Bestwick Ute‐Christiane Meier Mónica Marta Gloria Dalla Costa Tessel F. Runia E. P. Evdoshenko N. Lazareva Éric Thouvenot Pietro Iaffaldano Vita Direnzo Mohsen Khademi Fredrik Piehl Manuel Comabella M.H. Sombekke Joep Killestein Harald Hegen Stefan Rauch Sandra D’Alfonso JC Alvarez-Cermeño Pavlína Kleinová Dana Horáková Romy Roesler Florian Lauda Sara Llufriú Timuçin Avşar Uğur Uygunoğlu Ayşe Altıntaş Sabahattin Saip Til Menge Cecília Rajda Roberto Bergamaschi Natalia Moll Michael Khalil Romain Marignier Irena Dujmović Henrik Larsson Clas Malmeström Elio Scarpini Chiara Fenoglio Stig Wergeland Alice Laroni Viviana Annibali Silvia Romano A. Martinez Adriana Carrá Marco Salvetti Antonio Uccelli Øivind Torkildsen K-M Myhr Daniela Galimberti Konrad Rejdak Jan Lycke Jette Lautrup Frederiksen Jelena Drulović Cyrille B. Confavreux David Brassat Christian Enzinger Siegrid Fuchs Isabel Boscá Jean Pelletier Christophe Picard Elena Colombo D. Franciotta Tobias Derfuß RLP Lindberg Özgür Yaldizli László Vécsei BC Kieseier HP Hartung Pablo Villoslada Aksel Sıva Albert Saiz Hayrettin Tumani Eva Havrdová Luisa María Villar Maurizio Leone Nadia Barizzone Florian Deisenhammer C Teunissen Xavier Montalbán Mar Tintoré Tomas Olsson Maria Trojano Sylvain Lehmann Giovanni Castelnovo С. В. Лапин Rogier Hintzen L Kappos Roberto Furlan V Martinelli Giacomo P. Comi SV Ramagopalan Gavin Giovannoni

Background and objective: We explored which clinical biochemical variables predict conversion from clinically isolated syndrome (CIS) to definite multiple sclerosis (CDMS) in a large international cohort. Methods: Thirty-three centres provided serum samples 1047 CIS cases with at least two years’ follow-up. Age, sex, presentation, T2-hyperintense lesions, cerebrospinal fluid (CSF) oligoclonal bands (OCBs), CSF IgG index, cell count, 25-hydroxyvitamin D3 (25-OH-D), cotinine titres against...

10.1177/1352458514568827 article EN Multiple Sclerosis Journal 2015-02-13

Abstract Objective To evaluate cerebrospinal fluid ( CSF ) and serum neurofilament light chain (NfL) levels in genetic frontotemporal dementia FTD as a potential biomarker the presymptomatic stage during conversion into symptomatic stage. Additionally, to correlate NfL clinical neuroimaging parameters. Methods In this multicenter case–control study, we investigated 174 subjects (48 controls, 40 carriers 86 patients with microtubule‐associated protein tau MAPT ), progranulin GRN chromosome 9...

10.1002/acn3.325 article EN cc-by Annals of Clinical and Translational Neurology 2016-07-01

Neurofilament light chain (NfL) levels in the cerebrospinal fluid (CSF) of multiple sclerosis (MS) patients correlate with degree neuronal injury. To date, little is known about NfL concentrations serum relapsing remitting (RRMS) and their relationship CSF magnetic resonance imaging (MRI) measures disease severity. We aimed to validate quantification samples RRMS, as a biofluid source easily accessible for longitudinal studies.A total 31 RRMS underwent sampling. After median time 3.6 years,...

10.1177/1352458515623365 article EN Multiple Sclerosis Journal 2016-01-12

Neurofilaments are elevated in the cerebrospinal fluid (CSF) and serum of amyotrophic lateral sclerosis (ALS) patients. However, timing this increase is unknown. To characterize premanifest disease phase, we performed a cross-sectional study on asymptomatic (n = 12) symptomatic 64) ALS mutation carriers family controls 19). NF-L (neurofilament-light chain) pNF-H (phosphorylated neurofilament-heavy normal before symptom onset increased by at least an order magnitude early CSF (pNF-H) or...

10.1002/ana.24552 article EN Annals of Neurology 2015-11-03

<h3>Importance</h3> Unrecognized demyelinating events often precede the clinical onset of multiple sclerosis (MS). Identification these at time occurrence would have implications for early diagnosis and search causal factors disease. <h3>Objective</h3> To assess whether serum neurofilament light chain (sNfL) levels are elevated before MS onset. <h3>Design, Setting, Participants</h3> Nested case-control study among US military personnel who samples stored in Department Defense Serum...

10.1001/jamaneurol.2019.3238 article EN JAMA Neurology 2019-09-13
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