Original Research

Published on 11 Jan 2022

Clinical Courses of IKAROS and CTLA4 Deficiencies: A Systematic Literature Review and Retrospective Longitudinal Study

in Primary Immunodeficiencies

Akihiro Hoshino
Etsushi Toyofuku
Noriko Mitsuiki
Motoi Yamashita
Keisuke Okamoto
Michio Yamamoto
Kenji Kanda
Genki Yamato
Dai Keino
Yuri Yoshimoto-Suzuki

Frontiers in Immunology

doi 10.3389/fimmu.2021.784901

5,030 views
7 citations

Editorial

Published on 11 Jan 2022

Editorial: Immune-Related Non-Communicable Diseases in Africa

in Primary Immunodeficiencies

Mohamed-Ridha Barbouche
Brian Stephen Eley

Frontiers in Immunology

doi 10.3389/fimmu.2021.816257

2,431 views

Mini Review

Published on 10 Jan 2022

The Primary Immunodeficiency Database in Japan

in Primary Immunodeficiencies

Kanako Mitsui-Sekinaka
Yujin Sekinaka
Akifumi Endo
Kohsuke Imai
Shigeaki Nonoyama

Frontiers in Immunology

doi 10.3389/fimmu.2021.805766

5,339 views
4 citations

Original Research

Published on 10 Jan 2022

Fatigue Is Common in Immunoglobulin G Subclass Deficiency and Correlates With Inflammatory Response and Need for Immunoglobulin Replacement Therapy

in Primary Immunodeficiencies

Per Wågström
Åsa Nilsdotter-Augustinsson
Mats Nilsson
Janne Björkander
Charlotte Dahle
Sofia Nyström

Frontiers in Immunology

doi 10.3389/fimmu.2021.797336

30,381 views
7 citations

Original Research

Published on 04 Jan 2022

Autoimmune Cytopenias and Dysregulated Immunophenotype Act as Warning Signs of Inborn Errors of Immunity: Results From a Prospective Study

in Primary Immunodeficiencies

Ebe Schiavo
Beatrice Martini
Enrico Attardi
Filippo Consonni
Sara Ciullini Mannurita
Maria Luisa Coniglio
Marco Tellini
Elena Chiocca
Ilaria Fotzi
Laura Luti

Frontiers in Immunology

doi 10.3389/fimmu.2021.790455

8,385 views
18 citations

Original Research

Published on 03 Jan 2022

Implementation of Universal Newborn Screening for Severe Combined Immunodeficiency in Singapore While Continuing Routine Bacille-Calmette-Guerin Vaccination Given at Birth

in Primary Immunodeficiencies

Su-Wan Bianca Chan
Youjia Zhong
Soon Chuan James Lim
Sherry Poh
Kai Liang Teh
Jian Yi Soh
Chia Yin Chong
Koh Cheng Thoon
Michaela Seng
Ee Shien Tan

Frontiers in Immunology

doi 10.3389/fimmu.2021.794221

5,239 views
11 citations

Review

Published on 24 Dec 2021

Inborn Errors of Immunity in the Premature Infant: Challenges in Recognition and Diagnosis

in Primary Immunodeficiencies

Scott M. Gordon
Amy E. O’Connell

Frontiers in Immunology

doi 10.3389/fimmu.2021.758373

7,172 views
9 citations

Original Research

Published on 24 Dec 2021

Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1

in Primary Immunodeficiencies

Manfred Anim
Georgios Sogkas
Gunnar Schmidt
Natalia Dubrowinskaja
Torsten Witte
Reinhold Ernst Schmidt
Faranaz Atschekzei

Frontiers in Immunology

doi 10.3389/fimmu.2021.767188

4,015 views
5 citations

Case Report

Published on 22 Dec 2021

Case Report: Analysis of Preserved Umbilical Cord Clarified X-Linked Anhidrotic Ectodermal Dysplasia With Immunodeficiency in Deceased, Undiagnosed Uncles

in Primary Immunodeficiencies

Satoshi Inaba
Yuta Aizawa
Yuki Miwa
Chihaya Imai
Hidenori Ohnishi
Hirokazu Kanegane
Akihiko Saitoh

Frontiers in Immunology

doi 10.3389/fimmu.2021.786164

3,827 views
1 citation

Case Report

Published on 21 Dec 2021

Case Report: First Occurrence of Plasmablastic Lymphoma in Activated Phosphoinositide 3-Kinase δ Syndrome

in Primary Immunodeficiencies

Zexi Yin
Xin Tian
Runying Zou
Xiangling He
Keke Chen
Chengguang Zhu

Frontiers in Immunology

doi 10.3389/fimmu.2021.813261

2,265 views
6 citations

Original Research

Published on 21 Dec 2021

Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity: A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers

in Primary Immunodeficiencies

Kim Elsink
Manon M. H. Huibers
Iris H. I. M. Hollink
Annet Simons
Evelien Zonneveld-Huijssoon
Lars T. van der Veken
Helen L. Leavis
Stefanie S. V. Henriet
Marcel van Deuren
Frank L. van de Veerdonk

Frontiers in Immunology

doi 10.3389/fimmu.2021.780134

5,169 views
21 citations

Original Research

Published on 20 Dec 2021

Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity

in Primary Immunodeficiencies

Ludmila Perelygina
Raeesa Faisthalab
Emily Abernathy
Min-hsin Chen
LiJuan Hao
Lionel Bercovitch
Diana K. Bayer
Lenora M. Noroski
Michael T. Lam
Maria Pia Cicalese

Frontiers in Immunology

doi 10.3389/fimmu.2021.796065

6,715 views
26 citations

Case Report

Published on 20 Dec 2021

Case Report: Meningoencephalitis With Thrombotic Occlusive Vasculopathy in a Young EBV-Naïve Boy Is Associated With a Novel SH2D1A Mutation

in Primary Immunodeficiencies

Jolanda Steininger
Raphael Rossmanith
Christoph B. Geier
Alexander Leiss-Piller
Lukas Thonhauser
Simone Weiss
Johannes A. Hainfellner
Michael Freilinger
Wolfgang M. Schmidt
Martha M. Eibl

Frontiers in Immunology

doi 10.3389/fimmu.2021.747738

3,391 views
2 citations

Case Report

Published on 20 Dec 2021

Case Report: A New Gain-of-Function Mutation of STAT1 Identified in a Patient With Chronic Mucocutaneous Candidiasis and Rosacea-Like Demodicosis: An Emerging Association

in Primary Immunodeficiencies

Martin Martinot
Anne Sophie Korganow
Mathieu Wald
Julie Second
Elodie Birckel
Antoine Mahé
Laurent Souply
Mahsa Mohseni-Zadeh
Laure Droy
Julien Tarabeux

Frontiers in Immunology

doi 10.3389/fimmu.2021.760019

4,638 views
13 citations

Case Report

Published on 17 Dec 2021

Case Report: Fatal Complications of BK Virus-Hemorrhagic Cystitis and Severe Cytokine Release Syndrome Following BK Virus-Specific T-Cells

in Primary Immunodeficiencies

Elizabeth M. Holland
Corina Gonzalez
Elliot Levy
Vladimir A. Valera
Heather Chalfin
Jacquelyn Klicka-Skeels
Bonnie Yates
David E. Kleiner
Colleen Hadigan
Hema Dave

Frontiers in Immunology

doi 10.3389/fimmu.2021.801281

5,007 views
14 citations

Original Research

Published on 17 Dec 2021

Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study

in Primary Immunodeficiencies

Jessica Rojas-Restrepo
Andrés Caballero-Oteyza
Katrin Huebscher
Hanna Haberstroh
Manfred Fliegauf
Baerbel Keller
Robin Kobbe
Klaus Warnatz
Stephan Ehl
Michele Proietti

Frontiers in Immunology

doi 10.3389/fimmu.2021.786516

6,192 views
26 citations

Navigation group

Articles

Clinical Courses of IKAROS and CTLA4 Deficiencies: A Systematic Literature Review and Retrospective Longitudinal Study

Editorial: Immune-Related Non-Communicable Diseases in Africa

The Primary Immunodeficiency Database in Japan

Fatigue Is Common in Immunoglobulin G Subclass Deficiency and Correlates With Inflammatory Response and Need for Immunoglobulin Replacement Therapy

Autoimmune Cytopenias and Dysregulated Immunophenotype Act as Warning Signs of Inborn Errors of Immunity: Results From a Prospective Study

Implementation of Universal Newborn Screening for Severe Combined Immunodeficiency in Singapore While Continuing Routine Bacille-Calmette-Guerin Vaccination Given at Birth

Inborn Errors of Immunity in the Premature Infant: Challenges in Recognition and Diagnosis

Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1

Case Report: Analysis of Preserved Umbilical Cord Clarified X-Linked Anhidrotic Ectodermal Dysplasia With Immunodeficiency in Deceased, Undiagnosed Uncles

Case Report: First Occurrence of Plasmablastic Lymphoma in Activated Phosphoinositide 3-Kinase δ Syndrome

Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity: A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers

Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity

Case Report: Meningoencephalitis With Thrombotic Occlusive Vasculopathy in a Young EBV-Naïve Boy Is Associated With a Novel SH2D1A Mutation

Case Report: A New Gain-of-Function Mutation of STAT1 Identified in a Patient With Chronic Mucocutaneous Candidiasis and Rosacea-Like Demodicosis: An Emerging Association

Case Report: Fatal Complications of BK Virus-Hemorrhagic Cystitis and Severe Cytokine Release Syndrome Following BK Virus-Specific T-Cells

Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study