Robin Kobbe

ORCID: 0000-0001-6067-3408
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About
Contact & Profiles
Research Areas
  • Malaria Research and Control
  • SARS-CoV-2 and COVID-19 Research
  • COVID-19 Clinical Research Studies
  • Immunodeficiency and Autoimmune Disorders
  • Mosquito-borne diseases and control
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Migration, Health and Trauma
  • Long-Term Effects of COVID-19
  • HIV/AIDS Research and Interventions
  • Vaccine Coverage and Hesitancy
  • Blood disorders and treatments
  • Parasites and Host Interactions
  • Respiratory viral infections research
  • Travel-related health issues
  • HIV Research and Treatment
  • HIV/AIDS drug development and treatment
  • COVID-19 Impact on Reproduction
  • Immune responses and vaccinations
  • Immune Cell Function and Interaction
  • Viral gastroenteritis research and epidemiology
  • SARS-CoV-2 detection and testing
  • Dermatological diseases and infestations
  • Global Maternal and Child Health
  • COVID-19 and Mental Health
  • Tuberculosis Research and Epidemiology

Universität Hamburg
2016-2025

University Medical Center Hamburg-Eppendorf
2016-2025

Bernhard Nocht Institute for Tropical Medicine
2005-2025

Klinik und Poliklinik für Kinder- und Jugendmedizin
2009-2024

Center for Discovery
2024

Hackensack Meridian Health
2024

German Center for Infection Research
2016-2024

Friedrich Schiller University Jena
2024

Jena University Hospital
2024

University of Oxford
2021

Florian Götzinger Begoña Santiago Antoni Noguera‐Julián Miguel Lanaspa Laura Lancella and 95 more Francesca Ippolita Calò Carducci Natalia Gabrovska Svetlana Velizarova Petra Prunk Veronika Osterman Uroš Krivec Andrea Lo Vecchio Delane Shingadia Antoni Soriano‐Arandes Susana Melendo Marcello Lanari Luca Pierantoni Noémie Wagner Arnaud G. L’Huillier Ulrich Heininger Nicole Ritz Srini Bandi Nina Krajcar Srđan Roglić Mar Santos Christelle Christiaens Marine Creuven Danilo Buonsenso Steven B. Welch Matthias Bogyi Folke Brinkmann Marc Tebruegge Jasmin Pfefferle Angela Zacharasiewicz Angelika Berger Roland Berger Volker Strenger Daniela S. Kohlfürst Anna Zschocke Benoît Bernar Burkhard Simma Edda Haberlandt Christina Thir Ariane Biebl Koen Vanden Driessche Tine Boiy Daan Van Brusselen An Bael Sara Debulpaep Petra Schelstraete Ivan Pavić Ulrikka Nygaard Jonathan Peter Glenthoej Lise Jensen Ilona Lind Mihhail Tistsenko Ülle Uustalu Laura Buchtala Stephanie Thee Robin Kobbe Cornelius Rau Nicolaus Schwerk Michael Barker Μαρία Τσολιά Irini Eleftheriou Patrick J. Gavin O Kozdoba Borbála Zsigmond Piero Valentini Inga Ivaškevičienė Rimvydas Ivaškevičius Valentina Vilc Elisabeth H. Schölvinck A Rojahn Anastasios Smyrnaios Claus Klingenberg Í.T. De Carvalho Andreia Ribeiro Анна Старшинова Ivan Solovič Lola Falcón-Neyra Olaf Neth Laura Minguell Matilde Bustillo Alonso Aida M. Gutiérrez-Sánchez Borja Guarch Ibáñez Francesc Ripoll Beatriz Soto Karsten Kötz Petra Zimmermann Hanna Schmid Franziska Zucol A. Niederer Michael Buettcher Benhur Şirvan Çetin Olga Bilogortseva Vera Chechenyeva Alicia Demirjian Fiona Shackley Lynne McFetridge

10.1016/s2352-4642(20)30177-2 article EN other-oa The Lancet Child & Adolescent Health 2020-06-25

An outbreak caused by Shiga-toxin–producing Escherichia coli O104:H4 occurred in Germany May and June of 2011, with more than 3000 persons infected. Here, we report a cluster cases associated single family describe an open-source genomic analysis isolate from one member the family. This involved use rapid, bench-top DNA sequencing technology, data release, prompt crowd-sourced analyses. In less week, these studies revealed that strain belonged to enteroaggregative E. lineage had acquired...

10.1056/nejmoa1107643 article EN public-domain New England Journal of Medicine 2011-07-27

Human tuberculosis (TB) is caused by members of the Mycobacterium complex (MTBC). The MTBC comprises several human-adapted lineages known as M. sensu stricto, well two (L5 and L6) traditionally referred to africanum. Strains L5 L6 are largely limited West Africa for reasons unknown, little their genomic diversity, phylogeography evolution. Here, we analysed genomes 350 320 strains, isolated from patients 21 African countries, plus 5 related that had not been classified into any lineages. Our...

10.1099/mgen.0.000477 article EN cc-by Microbial Genomics 2021-02-01

In sub-Saharan Africa, malaria is a leading cause of morbidity and mortality among young children. Detailed knowledge spatial variation epidemiology associated risk factors important for planning evaluating malaria-control measures.The incidences socioeconomic were assessed over 21 months, from January 2003 to September 2005, in 535 children 9 villages small rural area with high Plasmodium falciparum transmission Ghana. Household positions mapped by use global positioning system, the effects...

10.1086/524066 article EN The Journal of Infectious Diseases 2007-12-04

Gain-of-function (GOF) mutations in the signal transducer and activator of transcription 1 (STAT1) result unbalanced STAT signaling cause immune dysregulation immunodeficiency. The latter is often characterized by susceptibility to recurrent Candida infections, resulting clinical picture chronic mucocutaneous candidiasis (CMC). This study aims assess frequency GOF STAT1 a large international cohort CMC patients. was sequenced genomic DNA from 57 patients 35 healthy family members. functional...

10.1007/s10875-015-0214-9 article EN cc-by Journal of Clinical Immunology 2015-11-25

Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous mutations NFKB2 have recently been established as a molecular cause of common variable immunodeficiency (CVID) and DAVID-syndrome, rare condition combining deficiency anterior pituitary hormone with CVID. Here, we investigate 15 previously unreported patients primary (PID) from eleven unrelated families heterozygous NFKB2-mutations including eight the p.Arg853* nonsense mutation five harboring unique novel...

10.3389/fimmu.2019.00297 article EN cc-by Frontiers in Immunology 2019-03-19

The transcription factor BCL11B is essential for development of the nervous and immune system, Bcl11b deficiency results in structural brain defects, reduced learning capacity, impaired cell mice. However, precise role humans largely unexplored, except a single patient with missense mutation, affected by multisystem anomalies profound deficiency. Using massively parallel sequencing we identified 13 patients bearing heterozygous germline alterations BCL11B. Notably, all them are global...

10.1093/brain/awy173 article EN Brain 2018-05-31
Tiziana Lorenzini Manfred Fliegauf Nils Klammer Natalie Frede Michele Proietti and 95 more Alla Bulashevska Nadezhda Camacho-Ordóñez Markku Varjosalo Matias Kinnunen Esther de Vries J.W.M. van der Meer Rohan Ameratunga Chaim M. Roifman Yael Dinur Schejter Robin Kobbe Timo Hautala Faranaz Atschekzei Reinhold E. Schmidt Claudia Schröder Polina Stepensky Bella Shadur Luis Alberto Pedroza Michiel van der Flier Mónica Martínez‐Gallo Luis Ignacio González‐Granado Luís M. Allende Anna Shcherbina N. B. Kuzmenko V.P. Zakharova João Farela Neves Peter Švec Ute Fischer Winnie Ip Oliver Bartsch Safa Barış Christoph Klein Raif S. Geha Janet Chou Mohammed F. Alosaimi Lauren Weintraub Kaan Boztuğ Tatjana Hirschmugl Maria Marluce dos Santos Vilela Dirk Holzinger Maximilian Seidl Vassilios Lougaris Alessandro Plebani Laia Alsina M. Piquer‐Gibert Àngela Deyà‐Martínez C Slade Asghar Aghamohammadi Hassan Abolhassani Lennart Hammarström Outi Kuismin Merja Helminen Hana Lango Allen James E. Thaventhiran Alexandra F. Freeman Matthew Cook Shahrzad Bakhtiar Mette Christiansen Charlotte Cunningham‐Rundles Niraj Patel William Rae Tim Niehues Nina Brauer Jaana Syrjänen Mikko Seppänen Siobhan O. Burns Paul Tuijnenburg Taco W. Kuijpers Klaus Warnatz Bodo Grimbacher Zoe Adhya Hana Alachkar Ariharan Anantharachagan Richard Antrobus Gururaj Arumugakani Sofie Ashford William J. Astle Anthony Attwood Chiara Bacchelli Joana Batista Helen Baxendale Claire Bethune Shahnaz Bibi Marta Bleda Barbara Boardman Claire Booth John R. Bradley Gerome Breen Matthew A. Brown Michael J. Browning Mary Brownlie Matthew Buckland Siobhan O. Burns Oliver S. Burren Keren Carss John C. Chambers

10.1016/j.jaci.2019.11.051 article EN Journal of Allergy and Clinical Immunology 2020-04-09

Children with human immunodeficiency virus type 1 (HIV-1) infection have limited options for effective antiretroviral treatment (ART).We conducted an open-label, randomized, noninferiority trial comparing three-drug ART based on the HIV integrase inhibitor dolutegravir standard care (non-dolutegravir-based ART) in children and adolescents starting first- or second-line ART. The primary end point was proportion of participants virologic clinical failure by 96 weeks, as estimated Kaplan-Meier...

10.1056/nejmoa2108793 article EN New England Journal of Medicine 2021-12-29

ODYSSEY showed superior efficacy for dolutegravir-based antiretroviral therapy (ART) versus standard of care (SOC) in children living with HIV starting first-line or second-line ART aged 4 weeks older. Here, we aim to compare virological outcomes and resistance the dolutegravir group SOC up 96 weeks. was an open-label, multicentre, randomised, non-inferiority trial done 29 centres seven countries (Germany, Spain, South Africa, Thailand, UK, Uganda, Zimbabwe). recruited at least 28 days...

10.1016/s2352-3018(24)00155-3 article EN cc-by The Lancet HIV 2025-02-01

Primary antibody deficiencies (PADs) are the most frequent primary immunodeficiencies in human subjects. The genetic causes of PADs largely unknown. Sec61 translocon alpha 1 subunit (SEC61A1) is major complex, which main polypeptide-conducting channel endoplasmic reticulum membrane. SEC61A1 a target gene spliced X-box binding protein and strongly induced during plasma cell (PC) differentiation.We identified novel defect studied its pathologic mechanism 11 patients from 2 unrelated families...

10.1016/j.jaci.2017.06.042 article EN publisher-specific-oa Journal of Allergy and Clinical Immunology 2017-08-04

Intermittent preventive antimalarial treatment in infants (IPTi) with sulfadoxine-pyrimethamine reduces falciparum malaria and anemia but has not been evaluated areas intense perennial transmission. It is unknown whether an additional the second year of life prolongs protection.A randomized, double-blinded, placebo-controlled trial administration therapy at 3, 9, 15 months age was conducted 1070 children area Ghana where holoendemic. Participants were monitored for 21 after recruitment...

10.1086/518575 article EN Clinical Infectious Diseases 2007-06-06

Abstract SARS-CoV-2 is the causative agent of COVID-19 and a severe threat to global health. Patients infected with show wide range symptoms disease severity, while limited data available on its immunogenicity. Here, kinetics development SARS-CoV-2-specific antibody responses in relation clinical features dynamics specific B-cell populations are reported. Immunophenotyping B cells was performed by flow cytometry longitudinally collected PBMCs. In parallel, serum samples were analyzed for...

10.1101/2020.04.14.20059733 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2020-04-17

Predominantly antibody deficiencies (PAD) are a heterogeneous group of disorders characterized by dysfunctional production, low immunoglobulin levels in serum and impaired vaccine responses. The clinical picture is variable, ranging from mild symptoms to severe complications, which may include autoimmunity, gastrointestinal disease, allergy, malignancies. If left untreated, PAD patients at risk enduring disease progression, irreversible organ damage, reduced life expectancy. A timely...

10.3389/fimmu.2021.786516 article EN cc-by Frontiers in Immunology 2021-12-17

Abstract Human parvovirus 4 has been considered to be transmitted only parenterally. However, after novel genotype 3 of was found in 2 patients with no parenteral risks, we tested infants Ghana. A viremia rate 8.6% over years indicates that this infection is common children Africa.

10.3201/eid1607.100025 article EN cc-by Emerging infectious diseases 2010-06-24

The identification and characterization of rare immune cell populations in humans can be facilitated by their growth advantage the context specific genetic diseases. Here, we use autoimmune lymphoproliferative syndrome to identify a population FAS-controlled TCRαβ+ T cells. They include CD4+, CD8+, double-negative cells defined CD38+CD45RA+T-BET− expression pattern. These unconventional are present healthy individuals, generated before birth, enriched lymphoid tissue, do not expand during...

10.1084/jem.20192191 article EN cc-by-nc-sa The Journal of Experimental Medicine 2020-11-10

So far, only a few reports about reinfections with SARS-CoV-2 have been published, and they often lack detailed immunological virological data. We report reinfection genetically distinct variant in an immunocompetent female healthcare worker that has led to mild disease course. No obvious viral escape mutations were observed the second virus variant. The infectious was shed from patient during infection episode despite presence of neutralizing antibodies her blood. Our data indicate moderate...

10.3390/v13040661 article EN cc-by Viruses 2021-04-12

Vulnerability to infectious diseases in refugees is dependent on country of origin, flight routes, and conditions. Information specific medical needs different groups lacking. We assessed the prevalence diseases, immunity vaccine-preventable chronic conditions children, adolescents, adult from Ukraine who arrived Germany 2022. Using media, we recruited Ukrainian at 13 sites between 9-12/2022. An antigen test for acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) infection, serologies...

10.1016/j.jiph.2024.02.003 article EN cc-by Journal of Infection and Public Health 2024-02-16
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