Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity

J Bustamante, S Boisson-Dupuis, L Abel… - Seminars in …, 2014 - Elsevier
Mendelian susceptibility to mycobacterial disease (MSMD) is a rare condition characterized
by predisposition to clinical disease caused by weakly virulent mycobacteria, such as BCG …

Inborn errors of IL-12/23-and IFN-γ-mediated immunity: molecular, cellular, and clinical features

O Filipe-Santos, J Bustamante, A Chapgier… - Seminars in …, 2006 - Elsevier
Mendelian susceptibility to mycobacterial diseases confers predisposition to clinical disease
caused by weakly virulent mycobacterial species in otherwise healthy individuals. Since …

2013 IDSA clinical practice guideline for vaccination of the immunocompromised host

LG Rubin, MJ Levin, P Ljungman… - Clinical infectious …, 2014 - academic.oup.com
An international panel of experts prepared an evidenced-based guideline for vaccination of
immunocompromised adults and children. These guidelines are intended for use by primary …

The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases

S Al-Muhsen, JL Casanova - Journal of allergy and clinical immunology, 2008 - Elsevier
Primary immunodeficiencies (PIDs) were long thought to be exclusively recessive traits—
autosomal recessive (AR) in most cases, with a few X-linked recessive (XR) diseases. In …

Vaccination in primary immunodeficiency disorders

A Sobh, FA Bonilla - The Journal of Allergy and Clinical Immunology: In …, 2016 - Elsevier
Immunocompromised patients have increased susceptibility to vaccine-preventable
infections. Thus, vaccination is a critical issue in this population. Vaccines are usually …

Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases

S Norouzi, A Aghamohammadi, S Mamishi… - Journal of Infection, 2012 - Elsevier
Primary immunodeficiency diseases (PIDs) are a group of inherited disorders, characterized
by defects of the immune system predisposing individuals to variety of manifestations …

Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds

C Prando, A Samarina, J Bustamante… - Medicine, 2013 - journals.lww.com
Abstract Autosomal recessive interleukin (IL)-12 p40 (IL-12p40) deficiency is a rare genetic
etiology of Mendelian susceptibility to mycobacterial disease (MSMD). We report the …

Primary immunodeficiency diseases and Bacillus Calmette-Guérin (BCG)-vaccine–derived complications: a systematic review

S Fekrvand, R Yazdani, P Olbrich, A Gennery… - The Journal of Allergy …, 2020 - Elsevier
Background Bacillus Calmette-Guérin (BCG) vaccine is a live attenuated bacterial vaccine
derived from Mycobacterium bovis, which is mostly administered to neonates in regions …

Neutralization of IFNγ defeats haemophagocytosis in LCMV‐infected perforin‐and Rab27a‐deficient mice

JP Schmid, CH Ho, F Chrétien, JM Lefebvre… - EMBO molecular …, 2009 - embopress.org
Hereditary haemophagocytic lymphohistiocytosis (HLH) is a fatal inflammatory disease and
treatments currently may lead to serious side effects. There is a pressing need for effective …

Fourth update on the Iranian National Registry of Primary Immunodeficiencies: integration of molecular diagnosis

H Abolhassani, F Kiaee, M Tavakol… - Journal of clinical …, 2018 - Springer
Background The number of inherited diseases and the spectrum of clinical manifestations of
primary immunodeficiency disorders (PIDs) are ever-expanding. Molecular diagnosis using …