Kyla J. Hildebrand

ORCID: 0000-0003-3825-8202
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About
Contact & Profiles
Research Areas
  • Food Allergy and Anaphylaxis Research
  • Immunodeficiency and Autoimmune Disorders
  • Asthma and respiratory diseases
  • Drug-Induced Adverse Reactions
  • Respiratory and Cough-Related Research
  • Eosinophilic Esophagitis
  • Pharmaceutical studies and practices
  • Respiratory viral infections research
  • Allergic Rhinitis and Sensitization
  • Blood disorders and treatments
  • Pediatric health and respiratory diseases
  • Immune Cell Function and Interaction
  • Pneumonia and Respiratory Infections
  • Viral gastroenteritis research and epidemiology
  • Immune Response and Inflammation
  • Immune responses and vaccinations
  • Celiac Disease Research and Management
  • Parvovirus B19 Infection Studies
  • Contact Dermatitis and Allergies
  • Infectious Diseases and Tuberculosis
  • Child and Adolescent Health
  • RNA modifications and cancer
  • Autoimmune and Inflammatory Disorders Research
  • Diabetes and associated disorders
  • NF-κB Signaling Pathways

British Columbia Children's Hospital
2016-2025

University of British Columbia
2016-2025

Western University
2012-2024

University of Toronto
2010-2024

3M (United States)
2024

Children's Hospital
2024

Public Health Ontario
2024

Community Research and Development Information Service
2023

Canadian Paediatric Society
2019-2021

Child and Family Research Institute
2013-2020

Ana García‐García Rebeca Pérez de Diego Carlos Flores Darawan Rinchai Jordi Solé‐Violán and 95 more Àngela Deyà‐Martínez Blanca García‐Solis José M. Lorenzo-Salazar Elisa Hernández-Brito Anna-Lisa Lanz Leen Moens Giorgia Bucciol Mohamed Almuqamam Joseph B. Domachowske Elena Colino Juan Luis Santos Francisco Manuel Marco de la Calle Claudio Pignata Aziz Bousfiha Stuart E. Turvey Stefanie Bauer Filomeen Haerynck J. Gonzálo Ocejo-Vinyals Francisco Lendínez Seraina Prader Nora Naumann‐Bartsch Jana Pachlopnik Schmid Catherine M. Biggs Kyla J. Hildebrand Alexandra Dreesman Miguel Ángel Cárdenes Fatima Ailal Ibtihal Benhsaien Giuliana Giardino Agueda Molina-Fuentes Clàudia Fortuny Swetha Madhavarapu Daniel Conway Carolina Prando Laire Schidlowski María T. Martínez-Saavedra Rafael Alfaro Felipè Rodríguez de Castro Gerhard Kindle Nizar Mahlaoui Markus G. Seidel Lougaris Vassilios Mikko Seppänen Laurent Abel Alessandro Aiuti Saleh Al‐Muhsen Fahd Al‐Mulla Mark S. Anderson Evangelos Andreakos Andrés A. Arias Hagit Baris Feldman Alexandre Bélot Catherine M. Biggs Dusan Bogunovic Alexandre Bolze Анастасія Бондаренко Ahmed Aziz Bousfiha Petter Brodin Yenan T. Bryceson Carlos D. Bustamante Manish J. Butte Giorgio Casari John Christodoulou Antônio Condino‐Neto Stefan N. Constantinescu Megan A. Cooper Clifton L. Dalgard Murkesh Desai Beth A. Drolet Jamila El Baghdadi Sara Elva Espinosa‐Padilla Jacques Fellay Carlos Flores José Luis Franco Antoine Froidure Peter K. Gregersen Bodo Grimbacher Filomeen Haerynck David Hagin Rabih Halwani Lennart Hammarström James R. Heath Sarah E. Henrickson Elena W.Y. Hsieh Eystein S. Husebye Kohsuke Imai Yuval Itan Erich D. Jarvis Timokratis Karamitros Kai Kisand Cheng‐Lung Ku YL Lau Yun Ling C. Lucas Tom Maniatis

X-linked recessive deficiency of TLR7, a MyD88- and IRAK-4–dependent endosomal ssRNA sensor, impairs SARS-CoV-2 recognition type I IFN production in plasmacytoid dendritic cells (pDCs), thereby underlying hypoxemic COVID-19 pneumonia with high penetrance. We report 22 unvaccinated patients autosomal MyD88 or IRAK-4 infected (mean age: 10.9 yr; 2 mo to 24 yr), originating from 17 kindreds eight countries on three continents. 16 were hospitalized: six moderate, four severe, critical pneumonia,...

10.1084/jem.20220170 article EN cc-by The Journal of Experimental Medicine 2023-03-03
Oriol Fornés Alicia Jia Hye Sun Kuehn Qing Min Ulrich Pannicke and 95 more Nikolai Schleußner Romane Thouenon Zhijia Yu María de los Angeles Astbury Catherine M. Biggs Miguel Galicchio Jorge Alberto Garcia-Campos Silvina Gismondi Guadalupe Villarreal Kyla J. Hildebrand Manfred Hönig Jia Hou Despina Moshous Stefania Pittaluga Xiaowen Qian Jacob Rozmus Ansgar Schulz Aidé Tamara Staines‐Boone Bijun Sun Jinqiao Sun Schauer Uwe Edna Venegas‐Montoya Wenjie Wang Xiaochuan Wang Wenjing Ying Xiaowen Zhai Qinhua Zhou Altuna Akalin Isabelle André‐Schmutz Thomas F.E. Barth Bernd Baumann Anne Brüstle Gaëtan Burgio Jacinta Bustamante Jean‐Laurent Casanova Marco G. Casarotto Marina Cavazzana Loïc Chentout Ian A. Cockburn Mariantonia Costanza Chaoqun Cui Oliver Daumke Kate L. Del Bel Hermann Eibel Xiaoqian Feng Vedran Franke J. Christof M. Gebhardt Andrea Götz Stephan Grunwald Bénédicte Hoareau Timothy R. Hughes Eva‐Maria Jacobsen Martin Janz Arttu Jolma Chantal Lagresle‐Peyrou Nannan Lai Yaxuan Li Susan Lin Henry Y. Lu Saúl Oswaldo Lugo Reyes Xin Meng Peter Möller Nidia Carolina Moreno‐Corona Julie E. Niemela Gherman Novakovsky Jareb J. Pérez-Caraballo Capucine Pïcard Lucie Poggi Emilia Puig Lombardi Katrina L. Randall Anja Reisser Yohann Schmitt Sandali Seneviratne Mehul Sharma Jennifer Stoddard Srinivasan Sundararaj Harry Sutton Linh Q. Tran Ying Wang Wyeth W. Wasserman Zichao Wen Wiebke Winkler Ermeng Xiong Ally Yang Meiping Yu Lumin Zhang Hai Zhang Qian Zhao Xin Zhen Anselm Enders Sven Kracker Rubén Martínez‐Barricarte Stephan Mathas Sergio D. Rosenzweig Klaus Schwarz

Interferon regulatory factor 4 (IRF4) is a transcription (TF) and key regulator of immune cell development function. We report recurrent heterozygous mutation in IRF4, p.T95R, causing an autosomal dominant combined immunodeficiency (CID) seven patients from six unrelated families. The exhibited profound susceptibility to opportunistic infections, notably Pneumocystis jirovecii , presented with agammaglobulinemia. Patients’ B cells showed impaired maturation, decreased immunoglobulin isotype...

10.1126/sciimmunol.ade7953 article EN Science Immunology 2023-01-13

Inborn errors of immunity (IEIs) are a group conditions whereby parts the immune system missing or dysfunctional. Once thought to primarily be pediatric disorder, it is now estimated that more than 50% worldwide incident IEI cases accounted for by adults. Delayed diagnosis, late symptom onset, and phenocopies can all lead adult-onset recognition IEIs. Lack awareness regarding diversity manifestations in adults contributes diagnostic treatment delays. Prompt referral immunology critical so...

10.1186/s13223-023-00862-8 article EN cc-by Allergy Asthma and Clinical Immunology 2024-01-17

Background: Age and certain medical/social conditions are risk factors for invasive pneumococcal disease (IPD).For prevention of IPD, the National Advisory Committee on Immunization (NACI) has recommended 23-valent polysaccharide vaccine, PNEU-P-23, adults 65 years age older over 18 living with underlying conditions.NACI also 13-valent conjugate PNEU-C-13, adults; however, in publicly funded programs, this recommendation is limited to individuals IPD.Two new vaccines, PNEU-C-15 PNEU-C-20,...

10.14745/ccdr.v49i23a08 article EN cc-by Canada Communicable Disease Report 2023-03-08

COVID-19 vaccination has been associated with anaphylaxis and hypersensitivity reactions. Infectious disease physicians allergists in the Canadian Special Immunization Clinic (SIC) Network developed guidance for evaluating patients adverse events following immunization (AEFI) including suspected hypersensitivity. This study evaluated management event recurrence subsequent vaccinations.

10.1016/j.vaccine.2024.06.045 article EN cc-by-nc Vaccine 2024-06-22

By March 2024, 40 cases had been reported (12 in 2023).[1][1] One measles case can cause infection 90% of exposed, unvaccinated people.[2][2] Complications occur 30% cases, most frequently children younger than 5 years; complications include otitis media, pneumonia,

10.1503/cmaj.240371 article EN cc-by-nc-nd Canadian Medical Association Journal 2024-04-21

Background Helios (encoded by IKZF2 ), a member of the Ikaros family transcription factors, is zinc finger protein involved in embryogenesis and immune function. Although predominantly recognised for its role development function T lymphocytes, particularly CD4 + regulatory cells (Tregs), expression extends beyond system. During embryogenesis, expressed wide range tissues, making genetic variants that disrupt strong candidates causing widespread immune-related developmental abnormalities...

10.1136/jmg-2022-109127 article EN Journal of Medical Genetics 2023-06-14

Inborn errors of immunity (IEIs) are a group conditions affecting immune system development and function. Due to their clinical heterogeneity lack provider awareness, patients suffer from long diagnostic delays that increase morbidity mortality. Next-generation sequencing facilitates earlier diagnosis treatment IEIs, but too often unable see the benefit this technology due gaps in providers' knowledge regarding which test barriers accessing sequencing.Here, we provide detailed phenotyping...

10.1111/pai.13571 article EN Pediatric Allergy and Immunology 2021-06-07
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