Abdullah Alangari

ORCID: 0000-0002-0104-8175
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About
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Research Areas
  • Immunodeficiency and Autoimmune Disorders
  • Asthma and respiratory diseases
  • Food Allergy and Anaphylaxis Research
  • Allergic Rhinitis and Sensitization
  • Respiratory and Cough-Related Research
  • Dermatology and Skin Diseases
  • Urticaria and Related Conditions
  • Contact Dermatitis and Allergies
  • Blood disorders and treatments
  • Immune Cell Function and Interaction
  • Mast cells and histamine
  • Gastrointestinal disorders and treatments
  • Autoimmune and Inflammatory Disorders Research
  • Drug-Induced Adverse Reactions
  • Pediatric health and respiratory diseases
  • interferon and immune responses
  • Inhalation and Respiratory Drug Delivery
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Tuberculosis Research and Epidemiology
  • Actinomycetales infections and treatment
  • Eosinophilic Esophagitis
  • Immune Response and Inflammation
  • S100 Proteins and Annexins
  • Myxozoan Parasites in Aquatic Species
  • Chronic Lymphocytic Leukemia Research

King Saud University
2013-2024

King Abdullah International Medical Research Center
2023

National Guard Health Affairs
2023

King Saud bin Abdulaziz University for Health Sciences
2023

King's College London
2023

Riyadh Armed Forces Hospital
2019

King Khalid University Hospital
2008-2012

University of Southampton
2008-2011

National Hospital
2010

Children's Hospital of Chongqing Medical University
2010

Ludovic de Beaucoudrey Arina Samarina Jacinta Bustamante Aurelié Cobat Stéphanie Boisson‐Dupuis and 95 more Jacqueline Feinberg Saleh Al‐Muhsen Lucile Jannière Y Rose Maylis de Suremain Xiao‐Fei Kong Orchidée Filipe‐Santos Ariane Chapgier Capucine Pïcard Alain Fischer Figen Doğu Aydan İkincioğulları Gönül Tanır Sami Al-Hajjar Suliman Aljumaah Husn H. Frayha Zobaida Alsum Sulaiman Al-Ajaji Abdullah Alangari Abdulaziz Al‐Ghonaium Parisa Adimi Naghan Davood Mansouri Imen Ben‐Mustapha Judith Yancoski Ben‐Zion Garty Carlos Rodríguez‐Gallego Isabel Caragol Necil Kütükçüler Dinakantha Kumararatne Smita Y. Patel Rainer Döffinger Andrew Exley Olle Jeppsson Janine Reichenbach David Nadal Yaryna Boyko Barbara Pietrucha Suzanne T. Anderson Michael Levin Liliane Schandené Kinda Schepers André Efira Françoise Mascart Masao Matsuoka Tatsunori Sakai Claire‐Anne Siegrist Klára Frecerová Renate Blüetters-Sawatzki Jutta Bernhöft Joachim Freihorst Ulrich Baumann Darko Richter Filomeen Haerynck Frans De Baets Vas Novelli David A. Lammas Christiane Vermylen David Tuerlinckx Chris Nieuwhof Małgorzata Pac W. Haas Ingrid Müller‐Fleckenstein Bernhard Fleckenstein Jacob Levy Revathi Raj Aileen Cleary Cohen David B. Lewis Steven M. Holland Kuender D. Yang Xiaochuan Wang Xiaohong Wang Liping Jiang Xiqiang Yang Chaomin Zhu Yuanyuan Xie Pamela Lee Koon Wing Chan Tong‐Xin Chen Gabriela Castro Ivelisse Natera Ana Codoceo Alejandra King Liliana Bezrodnik Daniela Di Giovani María Isabel Gaillard Dewton de Moraes Vasconcelos Anete Sevciovic Grumach Alberto José da Silva Duarte Ruth Aldana Francisco Espinosa‐Rosales Mohammed Bejaoui Ahmed Aziz Bousfiha Jamila El Baghdadi Namık Yaşar Özbek Güzide Aksu

Interleukin-12 receptor β1 (IL-12Rβ1) deficiency is the most common form of Mendelian susceptibility to mycobacterial disease (MSMD). We undertook an international survey 141 patients from 102 kindreds in 30 countries. Among probands, first infection occurred at a mean age 2.4 years. In 78 patients, this was caused by Bacille Calmette-Guérin (BCG; n = 65), environmental mycobacteria (EM; also known as atypical or nontuberculous mycobacteria) (n 9) Mycobacterium tuberculosis 4). Twenty-two...

10.1097/md.0b013e3181fdd832 article EN Medicine 2010-11-01

Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous autosomal recessive immune disorder characterized by the occurrence of uncontrolled activation lymphocytes and macrophages infiltrating multiple organs. Disease-causing mutations in perforin (PRF1; also known as FHL2), Munc13-4 (UNC13D; FHL3), syntaxin-11 (STX11; FHL4) genes have been identified individuals with FHL. These all encode proteins involved cytotoxic activity lymphocytes. Here, we show that gene...

10.1172/jci40732 article EN Journal of Clinical Investigation 2009-11-04

Herpes simplex encephalitis (HSE) is the most common sporadic viral of childhood. Autosomal recessive (AR) UNC-93B and TLR3 deficiencies autosomal dominant (AD) TRAF3 underlie HSE in some children. We report here unrelated children with AR or AD TRIF deficiency. The form disease was found to be due a homozygous nonsense mutation that resulted complete absence protein. Both TLR3- TRIF-dependent TLR4 signaling pathways were abolished. heterozygous missense mutation, resulting dysfunctional In...

10.1172/jci59259 article EN Journal of Clinical Investigation 2011-11-21

Deficiency of ubiquitin-specific peptidase 18 (USP18) is a severe type I interferonopathy. USP18 down-regulates interferon signaling by blocking the access Janus-associated kinase 1 (JAK1) to receptor. The absence results in unmitigated interferon-mediated inflammation and lethal during perinatal period. We describe neonate who presented with hydrocephalus, necrotizing cellulitis, systemic inflammation, respiratory failure. Exome sequencing identified homozygous mutation at an essential...

10.1056/nejmoa1905633 article EN New England Journal of Medicine 2020-01-15

To characterize the features of cold urticaria in children, with particular focus on systemic reactions, because little pediatric data are available.Chart reviews 30 children <18 years old who were evaluated past 3 at Children's Hospital Allergy Program (Boston, MA) and a private allergy practice. Demographic, diagnostic, therapeutic collected. Telephone interviews patients and/or their parents performed to obtain follow-up data.Our showed that mean median ages onset approximately 7 years....

10.1542/peds.113.4.e313 article EN PEDIATRICS 2004-04-01

Glucocorticoids are the mainstay of asthma therapy. They primarily used to suppress airway inflammation, which is central pathological change in asthmatic patients' airways. This achieved by many different mechanisms. The classical mechanism suppression genetic transcription inflammatory cytokines that key pathophysiology (transrepression). On other hand, certain inhibitory activated glucocorticoids (transactivation), a also mediates adverse effects glucocorticoids. onset action through...

10.4103/1817-1737.65040 article EN cc-by-nc-sa Annals of Thoracic Medicine 2010-01-01

IFN- γ has been used in the treatment of IL-12R β 1 deficiency patients with disseminated BCG infection (BCGosis), but optimal dose to reach efficacy is not clear. We a 2.7-year-old patient and refractory BCG-osis. IFN was started at 50 μ g/m 2 3 times per week. The upgraded 100 mcg/m after months, then 200 6 months afterwards. Serum mycobactericidal activity lymphocytes number function were evaluated throughout study. There no clinical response or doses. However, there some additional...

10.1155/2011/691956 article EN cc-by Clinical and Developmental Immunology 2010-12-22

Introduction As manuka honey (MH) exhibits immunoregulatory and anti-staphylococcal activities, we aimed to investigate if it could be effective in the treatment of atopic dermatitis (AD). Methods Adult volunteers with bilateral AD lesions were asked apply MH on one site overnight for seven consecutive days leave contralateral untreated as possible. Three Item Severity score was used evaluate response. Skin swabs obtained from both sites before after presence staphylococci enterotoxin...

10.1002/iid3.153 article EN cc-by Immunity Inflammation and Disease 2017-03-30

BackgroundInhaled corticosteroids, known to be effective as a maintenance medication in chronic asthma, have also been suggested therapy for acute asthma when given at high doses.MethodsA double-blind, randomized, placebo-controlled trial was conducted children aged 2 12 years with moderate or severe determined based on clinical score of 5 15 points, where is the most severe. We compared addition budesonide 1,500 μg vs placebo standard treatment, which included salbutamol, ipratropium...

10.1378/chest.13-2298 article EN cc-by-nc-nd CHEST Journal 2014-01-02

Alternative medicine is defined as medical therapies that are not regarded orthodox by the profession. The teaching of complementary and alternative (CAM) in schools becoming prevalent worldwide. Only a few studies have been done to assess students' attitude toward CAM need for courses.An observational, descriptive, cross-sectional study was conducted on students two universities, King Saud (KSU) Majmaah (MU) colleges, between February April 2015. A survey developed validated pilot study....

10.4103/jfcm.jfcm_98_17 article EN Journal of Family and Community Medicine 2018-01-01

Manuka honey (MH) is a complex nutritional material with antimicrobial, antioxidant and anti-inflammatory activity. We have previously shown that MH down regulates IL-4-induced CCL26 expression in immortalized keratinocytes. As contains potential ligands of the Aryl Hydrocarbon Receptor (AHR), key regulator skin homeostasis, we hypothesize this effect mediated via AHR activation. Here, treated HaCaT cell lines, either stable transfected an empty vector (EV-HaCaT) or which had been silenced...

10.1016/j.phrs.2023.106848 article EN cc-by Pharmacological Research 2023-07-05

BACKGROUND AND OBJECTIVES:Genetic association studies have demonstrated that over 100 variants in target genes (including ADAM33) are associated with airway remodeling and hyper-responsiveness different ethnic groups; however, this has never been evaluated Arabic populations.The objective of study was to determine whether ADAM33 polymorphisms asthma a population asthmatic children from Saudi Arabia. DESIGN SETTING:A cross-sectional pilot comparing the normal subjects patients Arabia period 1...

10.5144/0256-4947.2012.479 article EN cc-by-nc-nd Annals of Saudi Medicine 2012-09-01

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

Purine nucleoside phosphorylase (PNP) deficiency is a rare autosomal recessive metabolic disorder that results in combined immunodeficiency, neurologic dysfunction and autoimmunity. PNP has never been reported from Saudi Arabia or patients with an Arabic ethnic background. We report on two girls deficiency. Both showed severe lymphopenia neurological involvement. Sequencing of the gene one girl revealed novel missense mutation Pro146>Leu exon 4 due to change codon CCT>CTT. Expression (146L)...

10.4103/0256-4947.55320 article EN cc-by-nc-nd Annals of Saudi Medicine 2009-07-01

True allergic reactions to local anesthetics are extremely rare and constitute less than 1% of all reactions. In addition, many those caused by the preservative constituents anesthetics. Here we report a 12 year old girl with anaphylaxis lidocaine (an amide anesthetic) on two occasions. The allergy was confirmed positive skin prick test drug. Skin testing challenge another anesthetic (articaine) were negative. Subsequently, its use well tolerated in dental procedure. Up our knowledge, this...

10.1016/j.jsps.2013.10.001 article EN cc-by-nc-nd Saudi Pharmaceutical Journal 2013-10-12

Gastrointestinal basidiobolomycosis (GIB), caused by Basidiobolus ranrum, is a rare fungal infection with limited geographic distribution. The majority of the cases are reported from warm areas Arizona in USA, Saudi Arabia and Iran. We report middle aged patient who was admitted to hospital suspected metastatic colonic carcinoma. He presented constipation, anorexia weight loss. Computed tomography scan disclosed mass involving mid distal sigmoid colon hypodense lesion hepatic segment IV....

10.1016/j.idcr.2019.e00565 article EN cc-by-nc-nd IDCases 2019-01-01
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