Molecules great and small: the complement system

DR Mathern, PS Heeger - … Journal of the American Society of …, 2015 - journals.lww.com
The complement cascade, traditionally considered an effector arm of innate immunity
required for host defense against pathogens, is now recognized as a crucial pathogenic …

Progesterone and autoimmune disease

GC Hughes - Autoimmunity reviews, 2012 - Elsevier
Sexual dimorphism in human immune systems is most apparent in the female
predominance of certain autoimmune diseases (ADs) like systemic lupus erythematosus …

European evidence-based recommendations for diagnosis and treatment of childhood-onset systemic lupus erythematosus: the SHARE initiative

N Groot, N De Graeff, T Avcin… - Annals of the …, 2017 - ard.bmj.com
Childhood-onset systemic lupus erythematosus (cSLE) is a rare, multisystem and potentially
life-threatening autoimmune disorder with significant associated morbidity. Evidence-based …

The crossroads of autoimmunity and immunodeficiency: Lessons from polygenic traits and monogenic defects

B Grimbacher, K Warnatz, PFK Yong… - Journal of Allergy and …, 2016 - Elsevier
Autoimmune and immunodeficiency diseases are outcomes of a dysfunctional immune
system and represent 2 sides of the same coin. Multiple single-gene defects have been …

Complement and complement targeting therapies in glomerular diseases

S Andrighetto, J Leventhal, G Zaza… - International Journal of …, 2019 - mdpi.com
The complement cascade is part of the innate immune system whose actions protect hosts
from pathogens. Recent research shows complement involvement in a wide spectrum of …

Lupus manifestations in children with primary immunodeficiency diseases: comprehensive phenotypic and genetic features and outcome

SM Al-Mayouf, HA Alreefi, TA Alsinan… - Modern …, 2021 - academic.oup.com
Objectives To report the phenotypic, genetic findings and outcome of children with lupus
manifestations associated with primary immunodeficiency diseases (PIDs). Methods Data …

Phenotype and disease course differences in monogenic and sporadic childhood lupus

SM Al-Mayouf, F Alkhars, A AlSaleem - Lupus, 2023 - journals.sagepub.com
Objective To report the differences in phenotypic characteristics, disease course, and
outcome in monogenic and sporadic childhood lupus (SC-lupus) from a single tertiary …

Allogeneic hematopoietic stem cell transplantation in the treatment of human C1q deficiency: the Karolinska experience

RF Olsson, S Hagelberg, B Schiller, O Ringdén… - …, 2016 - journals.lww.com
Background Human C1q deficiency is associated with systemic lupus erythematosus (SLE)
and increased susceptibility to severe bacterial infections. These patients require extensive …

Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLE.

SM Al‐Mayouf, A AlSaleem, N AlMutairi… - International Journal …, 2018 - Wiley Online Library
Objective To report the clinical and genetic features of the first cases of chronic atypical
neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome …

Systemic lupus erythematosus with C1q deficiency: treatment with fresh frozen plasma

Z Ekinci, K Ozturk - Lupus, 2018 - journals.sagepub.com
Treatment and outcome of systemic lupus erythematosus (SLE) in C1q deficient patients are
rarely reported. The aim of this report is to share our experience about the course of …