Case Report

Published on 16 Jul 2024

Sweet syndrome associated with moderate leukocyte adhesion deficiency type I: a case report and review of the literature

in Primary Immunodeficiencies

Yoshine Saito
Anupama Kewalramani
Xiao P. Peng
Aimee Magnarelli
Howard M. Lederman

Frontiers in Immunology

doi 10.3389/fimmu.2024.1425289

940 views

Original Research

Published on 15 Jul 2024

Immune dysregulation due to bi-allelic mutation of the actin remodeling protein DIAPH1

in Primary Immunodeficiencies

Sagar Bhattad
Somashekara H. Ramakrishna
Ratan Kumar
Joseph M. Choi
Janet G. Markle

Frontiers in Immunology

doi 10.3389/fimmu.2024.1406781

1,037 views

Original Research

Accepted on 12 Jul 2024

The Effect of HLA Genotype on Disease Onset and Severity in CTLA-4 Insufficiency

in Primary Immunodeficiencies

Sara Posadas-Cantera
Noriko MITSUIKI
Florian Emmerich
Virginia Patiño
Hanns-Martin Lorenz
Olaf Neth
Ingunn Dybedal
Kjetil Taskén
Alejandro Schaffer
Bodo Grimbacher

Frontiers in Immunology

doi 10.3389/fimmu.2024.1447995

127 views

Original Research

Published on 12 Jul 2024

Flow cytometry-based diagnostic approach for inborn errors of immunity: experience from Algeria

in Primary Immunodeficiencies

Azzeddine Tahiat
Reda Belbouab
Abdelghani Yagoubi
Saliha Hakem
Faiza Fernini
Malika Keddari
Hayet Belhadj
Souad Touri
Samira Aggoune
Jennifer Stoddard

Frontiers in Immunology

doi 10.3389/fimmu.2024.1402038

2,276 views
1 citation

Case Report

Published on 09 Jul 2024

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report

in Primary Immunodeficiencies

Zhe Sun
Ruoqu Wei
Chaolan Pan
Cheng Ni
Xue Zhang
Wenbin Guan
Ruhong Cheng
Yan Gu
Hong Yu
Kejun He

Frontiers in Immunology

doi 10.3389/fimmu.2024.1414573

891 views
1 citation

Mini Review

Published on 08 Jul 2024

Expanding CXCR4 variant landscape in WHIM syndrome: integrating clinical and functional data for variant interpretation

in Primary Immunodeficiencies

Katarina Zmajkovicova
Keith Nykamp
Grace Blair
Melis Yilmaz
Jolan E. Walter

Frontiers in Immunology

doi 10.3389/fimmu.2024.1411141

1,192 views

Review

Published on 05 Jul 2024

The complex nature of CXCR4 mutations in WHIM syndrome

in Primary Immunodeficiencies

José Miguel Rodríguez-Frade
Luis Ignacio González-Granado
César A. Santiago
Mario Mellado

Frontiers in Immunology

doi 10.3389/fimmu.2024.1406532

1,532 views

Review

Published on 04 Jul 2024

Hem1 inborn errors of immunity: waving goodbye to coordinated immunity in mice and humans

in Primary Immunodeficiencies

Alexandra Christodoulou
Julia Y. Tsai
Nutthakarn Suwankitwat
Andreas Anderson
Brian M. Iritani

Frontiers in Immunology

doi 10.3389/fimmu.2024.1402139

1,331 views

Correction

Published on 28 Jun 2024

Corrigendum: Exploring the intersection of epigenetics, DNA repair, and immunology from studies of ICF syndrome, an inborn error of immunity

in Primary Immunodeficiencies

Motoko Unoki

Frontiers in Immunology

doi 10.3389/fimmu.2024.1445756

526 views

Original Research

Published on 28 Jun 2024

Nijmegen breakage syndrome: 25-year experience of diagnosis and treatment in Ukraine

in Primary Immunodeficiencies

Oksana Boyarchuk
Larysa Kostyuchenko
Hayane Akopyan
Anastasiia Bondarenko
Alla Volokha
Anna Hilfanova
Ihor Savchak
Liliia Nazarenko
Nataliia Yarema
Olha Urbas

Frontiers in Immunology

doi 10.3389/fimmu.2024.1428724

1,123 views

Original Research

Published on 27 Jun 2024

Charting a course for global progress in PIDs by 2030 — proceedings from the IPOPI global multi-stakeholders’ summit (September 2023)

in Primary Immunodeficiencies

Samya Van Coillie
Johan Prévot
Silvia Sánchez-Ramón
David M. Lowe
Michael Borg
Brigitte Autran
Gesmar Segundo
Antonio Pecoraro
Nicolas Garcelon
Cornelis Boersma

Frontiers in Immunology

doi 10.3389/fimmu.2024.1430678

1,558 views
1 citation

Original Research

Published on 26 Jun 2024

A degranulation assay using Vγ9Vδ2 T cells for the rapid diagnosis of familial hemophagocytic syndromes

in Primary Immunodeficiencies

Olivia Jorisch-Mühlebach
Dina Pitts
Raphaela Tinner
Hong Ying Teh
Conrad Roelli
Seraina Prader
Stefano Vavassori
Jana Pachlopnik Schmid

Frontiers in Immunology

doi 10.3389/fimmu.2024.1391967

1,262 views

Perspective

Published on 25 Jun 2024

Paving the way in implementation of SCID newborn screening in developing nations: feasibility study and strategies to move forward in Malaysia

in Primary Immunodeficiencies

Gaayathri Kumarasamy
Khayrin Khairiz
Wai Leng Chang
Thin Thin Aye
Adli Ali

Frontiers in Immunology

doi 10.3389/fimmu.2024.1400247

1,854 views
1 citation

Original Research

Published on 30 May 2024

Infection risk in patients with autoimmune cytopenias and immune dysregulation treated with mycophenolate mofetil and sirolimus

in Primary Immunodeficiencies

Mattia Comella
Elena Palmisani
Marcello Mariani
Gianluca Dell’Orso
Maria Licciardello
Maria Carla Giarratana
Luca Arcuri
Sara Pestarino
Alice Grossi
Marina Lanciotti

Frontiers in Immunology

doi 10.3389/fimmu.2024.1415389

1,099 views

Correction

Published on 29 May 2024

Corrigendum: Low rates of headache and migraine associated with intravenous immunoglobulin infusion using a 15-minute rate escalation protocol in 123 patients with primary immunodeficiency

in Primary Immunodeficiencies

Bob Geng
Kim Clark
Mark Evangelista
Eric Wolford

Frontiers in Immunology

doi 10.3389/fimmu.2024.1430313

489 views

Review

Published on 28 May 2024

MALT1 substrate cleavage: what is it good for?

in Primary Immunodeficiencies

Bahareh Nemati Moud
Franziska Ober
Thomas J. O’Neill
Daniel Krappmann

Frontiers in Immunology

doi 10.3389/fimmu.2024.1412347

2,487 views

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Articles

Sweet syndrome associated with moderate leukocyte adhesion deficiency type I: a case report and review of the literature

Immune dysregulation due to bi-allelic mutation of the actin remodeling protein DIAPH1

The Effect of HLA Genotype on Disease Onset and Severity in CTLA-4 Insufficiency

Flow cytometry-based diagnostic approach for inborn errors of immunity: experience from Algeria

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report

Expanding CXCR4 variant landscape in WHIM syndrome: integrating clinical and functional data for variant interpretation

The complex nature of CXCR4 mutations in WHIM syndrome

Hem1 inborn errors of immunity: waving goodbye to coordinated immunity in mice and humans

Corrigendum: Exploring the intersection of epigenetics, DNA repair, and immunology from studies of ICF syndrome, an inborn error of immunity

Nijmegen breakage syndrome: 25-year experience of diagnosis and treatment in Ukraine

Charting a course for global progress in PIDs by 2030 — proceedings from the IPOPI global multi-stakeholders’ summit (September 2023)

A degranulation assay using Vγ9Vδ2 T cells for the rapid diagnosis of familial hemophagocytic syndromes

Paving the way in implementation of SCID newborn screening in developing nations: feasibility study and strategies to move forward in Malaysia

Infection risk in patients with autoimmune cytopenias and immune dysregulation treated with mycophenolate mofetil and sirolimus

Corrigendum: Low rates of headache and migraine associated with intravenous immunoglobulin infusion using a 15-minute rate escalation protocol in 123 patients with primary immunodeficiency

MALT1 substrate cleavage: what is it good for?