Granulomatous disease in CVID: retrospective analysis of clinical characteristics and treatment efficacy in a cohort of 59 patients

…, M Malphettes, C Fieschi, L Galicier, D Boutboul… - Journal of clinical …, 2013 - Springer
Background Granulomatous disease (GD) will develop in a subset of patients with common
variable immunodeficiency (CVID). Little is known about the efficacy of therapeutic agents …

Microsporidiosis in solid organ transplant recipients: two Enterocytozoon bieneusi cases and review

F Lanternier, D Boutboul, J Menotti… - Transplant Infectious …, 2009 - Wiley Online Library
Microsporidiosis first came to prominence as an opportunistic infection in patients with acquired
immunodeficiency syndrome. Microsporidia are now emerging pathogens responsible …

Convalescent plasma therapy for B-cell–depleted patients with protracted COVID-19

…, M Michel, M Mahevas, D Boutboul… - Blood, The Journal …, 2020 - ashpublications.org
… (D) IL-6 was assessed in 5 patients at days −5 and +7, considering days 0 and +1 the
days of CPT. (F) ddPCR was assessed in 9 patients with a sensitivity threshold of 1.17 log (copies …

[HTML][HTML] Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: a cohort study

…, V Barlogis, T Asano, L Galicier, D Boutboul… - Journal of Allergy and …, 2016 - Elsevier
… AD, IgG (Fig 6, A), IgA (Fig 6, B), and IgM levels (Fig 6, C) and B-cell numbers (Fig 6, D) of
patients with APDS2 before onset of immunoglobulin replacement or other therapies. EH, CD4 …

Microbial ecology perturbation in human IgA deficiency

…, M Malphettes, L Galicier, D Boutboul… - Science translational …, 2018 - science.org
… (D) SIgA-binding levels of ex vivo purified and fixed microbiota are measured by a flow
cytometry–based assay. Gray histograms represent isotype control, and black lines represent anti-…

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

…, L Yun, C Thumerelle, E Oksenhendler, D Boutboul… - Medicine, 2012 - journals.lww.com
Autosomal dominant deficiency of signal transducer and activator of transcription 3 (STAT3)
is the main genetic etiology of hyper-immunoglobulin (Ig) E syndrome. We documented the …

Profound symptomatic hypogammaglobulinemia: a rare late complication after rituximab treatment for immune thrombocytopenia. Report of 3 cases and systematic …

R Levy, M Mahévas, L Galicier, D Boutboul… - Autoimmunity …, 2014 - Elsevier
Introduction B-cell depletion with rituximab (RTX) is widely used to treat autoimmune diseases,
especially as second-line therapy for immune thrombocytopenia (ITP). The incidence of …

Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

…, LF Reyes, M Garzaro, N Hatipoglu, D Boutboul… - Science …, 2023 - science.org
Life-threatening “breakthrough” cases of critical COVID-19 are attributed to poor or waning
antibody (Ab) response to SARS-CoV-2 vaccines in individuals already at risk. Preexisting …

Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect

…, G Mouillot, N Vince, D Boutboul… - Clinical Infectious …, 2009 - academic.oup.com
Background. Common variable immunodeficiency (CVID) is a primary immune deficiency
defined by defective antibody production. In most series, a small proportion of patients present …

The full spectrum of Castleman disease: 273 patients studied over 20 years

…, D Boutboul, D Fajgenbaum… - British Journal of …, 2018 - Wiley Online Library
… 2‐( 18 F)fluoro‐2‐deoxy‐D‐glucose positron emission tomography/computed tomography
was useful in 62 patients for staging/classification of the disease and for excluding associated …