The 2019 American College of Rheumatology/European league against rheumatism classification criteria for IgG4‐related disease

ZS Wallace, RP Naden, S Chari, H Choi… - Arthritis & …, 2020 - Wiley Online Library
Objective IgG4‐related disease (IgG4‐RD) can cause fibroinflammatory lesions in nearly
any organ. Correlation among clinical, serologic, radiologic, and pathologic data is required …

Natural killer cells in human autoimmune diseases

N Schleinitz, F Vély, JR Harlé, E Vivier - Immunology, 2010 - Wiley Online Library
Natural killer (NK) cells have been implicated in tumour surveillance and in the early control
of several microbial infections. In autoimmune disease their involvement in these processes …

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

JN Boursiquot, L Gérard, M Malphettes… - 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 …

[HTML][HTML] Association of COVID-19 inflammation with activation of the C5a–C5aR1 axis

J Carvelli, O Demaria, F Vély, L Batista… - Nature, 2020 - nature.com
Abstract Coronavirus disease 2019 (COVID-19) is a disease caused by infection with severe
acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and has resulted in a pandemic …

Long-term outcomes of autoimmune pancreatitis: a multicentre, international analysis

PA Hart, T Kamisawa, WR Brugge, JB Chung… - Gut, 2013 - gut.bmj.com
Objective Autoimmune pancreatitis (AIP) is a treatable form of chronic pancreatitis that has
been increasingly recognised over the last decade. We set out to better understand the …

Infections in 252 patients with common variable immunodeficiency

E Oksenhendler, L Gérard, C Fieschi… - Clinical Infectious …, 2008 - academic.oup.com
Background. Common variable immunodeficiency is characterized by recurrent infections
and defective immunoglobulin production. Methods. The DEFI French national study …

Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

A Fischer, J Provot, JP Jais, A Alcais… - Journal of Allergy and …, 2017 - Elsevier
Background Primary immunodeficiencies (PIDs) are inherited diseases associated with a
considerable increase in susceptibility to infections. It is known that PIDs can also …

Severe imbalance of IL-18/IL-18BP in patients with secondary hemophagocytic syndrome

K Mazodier, V Marin, D Novick, C Farnarier, S Robitail… - Blood, 2005 - ashpublications.org
Hemophagocytic syndrome (HPS) is characterized by an uncontrolled and poorly
understood activation of T-helper 1 (Th-1) lymphocytes and macrophages. We studied 20 …

High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody

Y Allenbach, J Keraen, A Bouvier, V Jooste… - Brain, 2016 - academic.oup.com
Cancer can occur in patients with inflammatory myopathies. This association is mainly
observed in dermatomyositis, and myositis-specific antibodies have allowed us to delineate …

IgG4-related systemic disease: features and treatment response in a French cohort: results of a multicenter registry

M Ebbo, L Daniel, M Pavic, P Sève, M Hamidou… - Medicine, 2012 - journals.lww.com
IgG4-related systemic disease is now recognized as a systemic disease that may affect
various organs. The diagnosis is usually made in patients who present with elevated IgG4 in …