Mohammed F. Alosaimi

ORCID: 0000-0002-8025-3491
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About
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Research Areas
  • Immunodeficiency and Autoimmune Disorders
  • Immune Cell Function and Interaction
  • SARS-CoV-2 and COVID-19 Research
  • COVID-19 Clinical Research Studies
  • Diabetes and associated disorders
  • Long-Term Effects of COVID-19
  • interferon and immune responses
  • Blood disorders and treatments
  • Immune Response and Inflammation
  • NF-κB Signaling Pathways
  • Cytomegalovirus and herpesvirus research
  • Neonatal Respiratory Health Research
  • Autoimmune and Inflammatory Disorders Research
  • Viral-associated cancers and disorders
  • IoT and Edge/Fog Computing
  • Parvovirus B19 Infection Studies
  • T-cell and B-cell Immunology
  • Virus-based gene therapy research
  • Viral Infections and Outbreaks Research
  • Thyroid Disorders and Treatments
  • Wound Healing and Treatments
  • Adenosine and Purinergic Signaling
  • Privacy-Preserving Technologies in Data
  • SARS-CoV-2 detection and testing
  • Dental Erosion and Treatment

King Saud University
2018-2025

Cardiff University
2023

King Khalid University Hospital
2021-2023

Umm al-Qura University
2021

King Abdul Aziz University Hospital
2021

Boston Children's Hospital
2018-2020

Harvard University
2018-2020

Qian Zhang Paul Bastard Zhiyong Liu Jérémie Le Pen Marcela Moncada‐Vélez and 95 more Jie Chen Masato Ogishi Ira K. D. Sabli Stephanie Hodeib Cecilia B. Korol Jérémie Rosain Kaya Bilgüvar Junqiang Ye Alexandre Bolze Benedetta Bigio Rui Yang Andrés A. Arias Qinhua Zhou Yu Zhang Fanny Onodi Sarantis Korniotis Léa Karpf Quentin Philippot Marwa Chbihi Lucie Bonnet‐Madin Karim Dorgham Nikaïa Smith William M. Schneider Brandon S. Razooky Hans-Heinrich Hoffmann Eleftherios Michailidis Leen Moens Ji Eun Han Lazaro Lorenzo Lucy Bizien Philip Meade Anna‐Lena Neehus Aileen Camille Ugurbil Aurélien Corneau Gaspard Kerner Peng Zhang Franck Rapaport Yoann Seeleuthner Jérémy Manry Cécile Masson Yohann Schmitt Agatha Schlüter Tom Le Voyer Taushif Khan Juan Li Jacques Fellay Lucie Roussel Mohammad Shahrooei Mohammed F. Alosaimi Davood Mansouri Haya Al‐Saud Fahd Al‐Mulla Feras Almourfi Saleh Zaid Al-Muhsen Fahad Alsohime Saeed Al Turki Rana Hasanato Diederik van de Beek Andrea Biondi Laura Rachele Bettini Mariella D’Angiò Paolo Bonfanti Luisa Imberti Alessandra Sottini Simone Paghera Eugenia Quirós-Roldán Camillo Rossi Andrew J. Oler Miranda F. Tompkins Camille Alba Isabelle Vandernoot Jean‐Christophe Goffard Guillaume Smits Isabelle Migeotte Filomeen Haerynck Pere Soler‐Palacín Andrea Martín-Nalda Roger Colobrán Pierre‐Emmanuel Morange Sevgi Keleş Fatma Çölkesen Tayfun Özçelık Kadriye Kart Yaşar Sevtap Şenoğlu Şemsi̇ Nur Karabela Carlos Rodríguez‐Gallego Giuseppe Novelli Sami Hraiech Yacine Tandjaoui-Lambiotte Xavier Duval Cédric Laouénan Andrew L. Snow Clifton L. Dalgard Joshua D. Milner Donald C. Vinh

The genetics underlying severe COVID-19 immune system is complex and involves many genes, including those that encode cytokines known as interferons (IFNs). Individuals lack specific IFNs can be more susceptible to infectious diseases. Furthermore, the autoantibody dampens IFN response prevent damage from pathogen-induced inflammation. Two studies now examine likelihood affects risk of coronavirus disease 2019 (COVID-19) through components this (see Perspective by Beck Aksentijevich). Q....

10.1126/science.abd4570 article EN cc-by Science 2020-09-24
Daniela Matuozzo Estelle Talouarn Astrid Marchal Peng Zhang Jérémy Manry and 95 more Yoann Seeleuthner Yu Zhang Alexandre Bolze Matthieu Chaldebas Baptiste Milisavljevic Adrian Gervais Paul Bastard Takaki Asano Lucy Bizien Federica Barzaghi Hassan Abolhassani Ahmad Abou Tayoun Alessandro Aiuti Ilad Alavi Darazam Luis M. Allende Rebeca Alonso‐Arias Andrés A. Arias Gökhan Aytekіn Peter Bergman Simone Bondesan Yenan T. Bryceson Ingrid G. Bustos Óscar Cabrera-Marante Sheila Cárcel Paola Carrera Giorgio Casari Khalil Chaïbi Roger Colobrán Antônio Condino‐Neto Laura Covill Ottavia M. Delmonte Loubna El Zein Carlos Flores Peter K. Gregersen Marta Gut Filomeen Haerynck Rabih Halwani Selda Hançerli Lennart Hammarström Nevin Hatipoğlu Adem Karbuz Sevgi Keleş Christèle Kyheng Rafael León‐López José Luis Franco Davood Mansouri Javier Martínez‐Picado Özge Metin Akcan Isabelle Migeotte Pierre‐Emmanuel Morange Guillaume Morelle Andrea Martín-Nalda Giuseppe Novelli Antonio Novelli Tayfun Özçelık Figen Palabıyık Qiang Pan‐Hammarström Rebeca Pérez de Diego Laura Planas‐Serra Daniel E. Pleguezuelo Carolina Prando Aurora Pujol Luis Felipe Reyes Jacques G. Rivière Carlos Rodríguez‐Gallego Julián Rojas Patrizia Rovere‐Querini Agatha Schlüter Mohammad Shahrooei Ali Sobh Pere Soler‐Palacín Yacine Tandjaoui-Lambiotte Imran Tipu Cristina Tresoldi Jesús Troya Diederik van de Beek Mayana Zatz Paweł Zawadzki Saleh Zaid Al-Muhsen Mohammed F. Alosaimi Fahad Alsohime Hagit Baris Feldman Manish J. Butte Stefan N. Constantinescu Megan A. Cooper Clifton L. Dalgard Jacques Fellay James R. Heath YL Lau Richard P. Lifton Tom Maniatis Trine H. Mogensen Horst von Bernuth Alban Lermine Michel Vidaud

Abstract Background We previously reported that impaired type I IFN activity, due to inborn errors of TLR3- and TLR7-dependent interferon (IFN) immunity or autoantibodies against IFN, account for 15–20% cases life-threatening COVID-19 in unvaccinated patients. Therefore, the determinants remain be identified ~ 80% cases. Methods report here a genome-wide rare variant burden association analysis 3269 patients with COVID-19, 1373 SARS-CoV-2-infected individuals without pneumonia. Among 928...

10.1186/s13073-023-01173-8 article EN cc-by Genome Medicine 2023-04-05
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

Human cells homozygous for rare loss-of-expression (LOE) TYK2 alleles have impaired, but not abolished, cellular responses to IFN-α/β (underlying viral diseases in the patients) and IL-12 IL-23 mycobacterial diseases). Cells common P1104A allele selectively impaired isolated disease). We report three new forms of deficiency six patients from five families (R864C, G996R, G634E, or G1010D) compound heterozygous a (A928V). All these missense encode detectable proteins. The R864C G1010D are...

10.1084/jem.20220094 article EN cc-by The Journal of Experimental Medicine 2022-09-12

STAT2 is a transcription factor activated by type I and III interferons. We report 23 patients with loss of function variants causing autosomal recessive (AR), complete deficiency. Both cells transfected mutant alleles the patients' display impaired expression interferon stimulated genes control in-vitro viral infections. Clinical manifestations from early childhood onward include severe adverse reaction to live attenuated vaccines (LAV, 12/17 patients) infections (10/23 patients),...

10.1172/jci168321 article EN cc-by Journal of Clinical Investigation 2023-03-28

Background Post-acute coronavirus disease 2019 (COVID-19) syndrome, also known as long COVID, is a prolonged illness after the acute phase of COVID-19. Hospitalized patients were to have persisting symptoms fatigue, headache, dyspnea, and anosmia. There need describe characteristics individuals with post-COVID-19 in comparison baseline characteristics. Purpose To investigate clinical biochemical people who recovered from COVID-19 6 months discharge hospital. Methods This was prospective...

10.3389/fmed.2022.1067082 article EN cc-by Frontiers in Medicine 2022-12-06
Romain Lévy Florian Gothe Mana Momenilandi Thomas Magg Marie Materna and 95 more Philipp Peters Johannes Raedler Quentin Philippot Anita Rack-Hoch David Langlais Mathieu Bourgey Anna-Lisa Lanz Masato Ogishi Jérémie Rosain Emmanuel Martin Sylvain Latour Natasha Vladikine Marco Distefano Taushif Khan Franck Rapaport M. Schulz Ursula Holzer Anders Fasth Georgios Sogkas Carsten Speckmann Arianna Troilo Venetia Bigley Anna Roppelt Yael Dinur-Schejter Ori Toker Karen Helene Bronken Martinsen Roya Sherkat Ido Somekh Raz Somech Dror S. Shouval Jörn‐Sven Kühl Winnie Ip Elizabeth McDermott Lucy Cliffe Ahmet Özen Safa Barış Hemalatha G. Rangarajan Emmanuelle Jouanguy Anne Puel Jacinta Bustamante Marie‐Alexandra Alyanakian Mathieu Fusaro Yi Wang Xiao‐Fei Kong Aurélie Cobat David Boutboul Martin Castelle Claire Aguilar Olivier Hermine Morgane Cheminant Félipe Suarez Alişan Yıldıran Aziz Bousfiha Hamoud Al‐Mousa Fahad Alsohime Deniz Çağdaş Roshini S. Abraham Alan P. Knutsen Børre Fevang Sagar Bhattad Ayça Kıykım Baran Erman Tugba Arıkoğlu Ekrem Ünal Ashish Kumar Christoph B. Geier Ulrich Baumann Bénédicte Neven Julie Calas Elizabeth Feuille Angela Chan Gözde Yeşil Justine Nammour Élise Bandet Capucine Pïcard Ibtihal Benhsaien Peter Lang Faranaz Atschekzei Klaus Warnatz Sophie Hambleton Mukesh Desai Elif Karakoç-Aydıner Burcu Kolukısa Saleh Al‐Muhsen Mohammed F. Alosaimi Funda Çipe Anas M. Alazami Gonca Hancıoğlu Bilge Can Meydan Hanne Sørmo Sorte Asbjørg Stray‐Pedersen Geetha Mammayil Nazan Tökmeci Anna Shcherbina Polina Stepensky

Patients with inherited CARMIL2 or CD28 deficiency have defective T cell signaling, but their immunological and clinical phenotypes remain largely unknown. We show that only one of three isoforms is produced functional across leukocyte subsets. Tested mutant alleles from 89 patients 52 families impair canonical NF-κB not AP-1 NFAT activation in cells stimulated via CD28. Like CD28-deficient patients, CARMIL2-deficient display recalcitrant warts low blood counts CD4+ CD8+ memory TREGs. Unlike...

10.1084/jem.20220275 article EN cc-by The Journal of Experimental Medicine 2022-12-14

<title>Abstract</title> Objective To achieve consensus on the definition and clinical approach of Monogenic Inflammatory Immune Dysregulation Disorders (MIIDDs), a collective term for rare conditions marked by inflammation, immune dysregulation, infection susceptibility. Methods A multi-step, evidence-based, multidisciplinary process was employed, consisting of: 1) systematic literature review across four electronic databases (Cochrane Library, Web Science, Scopus, MEDLINE via PubMed),...

10.21203/rs.3.rs-5942561/v1 preprint EN cc-by Research Square (Research Square) 2025-02-06

There are limited data on the efficacy and safety of favipiravir antiviral in coronavirus disease 2019 (COVID-19), particularly more progressed phase. This study aims to evaluate effect reducing length hospital stay in-hospital mortality among moderate severe hospitalized COVID-19 patients.A prospective, multicenter observational was conducted that included adult patients four major regions (Riyadh (Riyadh), Eastern (Dammam), Al-Qassem (Buraydah), Macca (Jeddah) Saudi Arabia. For primary...

10.3389/fmed.2022.826247 article EN cc-by Frontiers in Medicine 2022-03-04

CBL-B is an E3 ubiquitin ligase that ubiquitinates proteins downstream of immune receptors to downregulate positive signaling cascades. Distinct homozygous mutations in CBLB were identified 3 unrelated children with early-onset autoimmunity, one whom also had chronic urticaria. Patient T cells exhibited hyperproliferation response anti-CD3 cross-linking. One the mutations, p.R496X, abolished expression, and a second mutation, p.C464W, resulted preserved expression. The third p.H285L SH2...

10.1172/jci154487 article EN cc-by Journal of Clinical Investigation 2022-08-25

The severe manifestation of coronavirus disease 2019 (COVID-19) is known to be mediated by several cytokines and chemokines. study aimed compare the early cytokine profile mild COVID-19 patients that with COVID-19-like symptoms tested negative for Severe Acute Respiratory Syndrome Coronavirus-2 in Reverse-Transcriptase Polymerase Chain Reaction (RT-PCR) test.This was a prospective, observational on admitted King Khalid University Hospital, Saud Medical City from June November 2020. Clinical...

10.2147/jir.s408663 article EN cc-by-nc Journal of Inflammation Research 2023-06-01

COVID-19 is diagnosed using RT-PCR assays of samples from nasal and oropharyngeal swabs. People with negative often presented clinical manifestations COVID-19. The data on such patients are lacking. present study aims to characterize the who were suspected cases tested in compared had been positive.This a retrospective, observational adult confirmed admitted King Saud University Medical City, Riyadh, Saudi Arabia, 1st March 2020 until 30th November 2020. Laboratory confirmation done through...

10.1016/j.jiph.2021.09.014 article EN cc-by-nc-nd Journal of Infection and Public Health 2021-09-23

Enamel demineralization and white-spot lesions (WSLs) around the orthodontic brackets are common clinical complications after fixed appliance therapy. WSLs form mainly due to plaque deposition during treatment period. This study was designed compare evaluate efficacy of two different remineralization agents on WSLs, which “Clinpro 5000 Colgate Sensitive Pro-Relief”. 27 caries-free human premolar teeth were collected extraction for purposes. The crowns set in acrylic resin, entire surfaces...

10.1155/2021/6644069 article EN cc-by International Journal of Dentistry 2021-01-18

Cardiovascular disease is one of the main causes hospital admission and mortality, thyroid dysfunction increases risk developing acute or exacerbation chronic cardiac conditions. The aim this study to investigate prevalence hormone abnormality among patients in care unit (CCU) its relation diagnosis, clinical, biochemical data, hospital-related outcomes.We conducted a retrospective cohort observational that included adult who were admitted CCU. We excluded those with known received...

10.2147/ijgm.s292750 article EN cc-by-nc International Journal of General Medicine 2021-02-01
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