Complement and antibody primary immunodeficiency in juvenile systemic lupus erythematosus patients

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Lupus

• Publication date

  2011-08-03

• Fields of study

  Medicine

• Identifiers
  DOI 10.1177/0961203311411598PMID 21813590
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• The efficacy of tacrolimus in patients with interstitial lung diseases complicated with polymyositis or dermatomyositis

  2014cited by this paper
• Selective IgA Deficiency

  2010cited by this paper
• Anti‐C1q Antibodies in Juvenile‐Onset Systemic Lupus Erythematosus

  2009cited by this paper
• Management of hypogammaglobulinaemia occurring in patients with systemic lupus erythematosus.

  2008cited by this paper
• Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.

  2008cited by this paper
• Disorders of Apoptosis: Mechanisms for Autoimmunity in Primary Immunodeficiency Diseases

  2008cited by this paper
• Understanding Systemic Lupus Erythematosus Physiopathology in the Light of Primary Immunodeficiencies

  2008cited by this paper
• Lack of Association of VDR Gene Polymorphisms with Thyroid Autoimmune Disorders: Familial and Case/Control Studies

  2007cited by this paper
• Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.

  2007cited by this paper
• Reversible hypogammaglobulinaemia.

  2007cited by this paper
• The validity of the inclusion of "lupus headache" in the Systemic Lupus Erythematosus Disease Activity Index.

  2007cited by this paper
• Hereditary Complement Deficiency and Lupus

  2007cited by this paper
• Tolerance and autoimmunity: lessons at the bedside of primary immunodeficiencies.

  2007cited by this paper
• Common variable immunodeficiency in systemic lupus erythematosus.

  2007cited by this paper
• Complement deficiencies and systemic lupus erythematosus

  2007cited by this paper
• Selective IgA deficiency in children and adults with systemic lupus erythematosus

  2007cited by this paper
• A Defect of Regulatory T Cells in Patients with Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy1

  2007cited by this paper
• Cutaneous and other lupus‐like symptoms in carriers of X‐linked chronic granulomatous disease: incidence and autoimmune serology

  2007cited by this paper
• X-Linked Agammaglobulinemia: Report on a United States Registry of 201 Patients

  2006cited by this paper
• Phenotype-genotype association grid: a convenient method for summarizing multiple association analyses

  2006cited by this paper
• Which complement assays and typings are necessary for the diagnosis of complement deficiency in patients with lupus erythematosus? A study of 25 patients.

  2006cited by this paper
• Abnormal apoptosis in chronic granulomatous disease and autoantibody production characteristic of lupus.

  2006cited by this paper
• Role of complement and other innate immune mechanisms in the removal of apoptotic cells.

  2006cited by this paper
• The health status and quality of life of adults with X-linked agammaglobulinemia.

  2006cited by this paper
• Real-time PCR quantification of human complement C4A and C4B genes

  2006cited by this paper
• Orphanet Journal of Rare Diseases BioMed Central Review

  2006cited by this paper
• International pediatric sepsis consensus conference: Definitions for sepsis and organ dysfunction in pediatrics*

  2005cited by this paper
• Thymic commitment of regulatory T cells is a pathway of TCR-dependent selection that isolates repertoires undergoing positive or negative selection.

  2005cited by this paper
• IGM is required for efficient complement mediated phagocytosis of apoptotic cells in vivo

  2005cited by this paper
• The intricate role of complement component C4 in human systemic lupus erythematosus.

  2004cited by this paper
• The role of complement in the development of systemic lupus erythematosus.

  2004cited by this paper
• Autoimmunity in Wiskott-Aldrich syndrome

  2003cited by this paper
• Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study.

  2002cited by this paper
• Systemic lupus erythematosus disease activity index 2000.

  2002cited by this paper
• Analysis of human leukocyte antigens class II-DR in Brazilian children and adolescents with systemic lupus erythematosus.

  2002cited by this paper
• Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome

  2002cited by this paper
• Deficiency in Serum Immunoglobulin (Ig)m Predisposes to Development of Igg Autoantibodies

  2000cited by this paper
• Lupus erythematosus associated with genetically determined deficiency of the second component of the complement.

  2000cited by this paper
• Accelerated development of IgG autoantibodies and autoimmune disease in the absence of secreted IgM.

  2000cited by this paper
• Systemic lupus erythematosus, complement deficiency, and apoptosis.

  2000cited by this paper
• Chronic Granulomatous Disease: Report on a National Registry of 368 Patients

  2000cited by this paper
• Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition.

  1999cited by this paper
• Cardiac tamponade due to systemic lupus erythematosus in a 7-year-old boy with selective IgG subclass deficiency

  1998cited by this paper
• Clinical review 93: Autoimmune polyglandular syndrome type 1.

  1998cited by this paper
• IgA deficiency and SLE: prevalence in a clinic population and a review of the literature

  1997cited by this paper
• Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus.

  1997cited by this paper
• C1q binds directly and specifically to surface blebs of apoptotic human keratinocytes: complement deficiency and systemic lupus erythematosus revisited.

  1997cited by this paper
• Combined Heterozygous Deficiency of the Classical Complement Pathway Proteins C2 and C4

  1997cited by this paper
• The reliability of the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index in patients with systemic lupus erythematosus.

  1997cited by this paper
• C2 deficiency in blood donors and lupus patients: prevalence, clinical characteristics and HLA-associations in the Brazilian population

  1997cited by this paper
• Type II Human Complement C2 Deficiency

  1996cited by this paper
• IgM deficiency in systemic lupus erythematosus patients.

  1995cited by this paper
• Linkage of IgA deficiency to Gm allotypes; the influence of Gm allotypes on IgA‐IgG subclass deficiency

  1995cited by this paper
• Invariance and restriction toward a limited set of self-antigens characterize neonatal IgM antibody repertoires and prevail in autoreactive repertoires of healthy adults.

  1995cited by this paper
• Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.

  1993cited by this paper
• Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.

  1992cited by this paper
• Selective IgA deficiency.

  1988cited by this paper
• IgM reduction in systemic lupus erythematosus.

  1988cited by this paper
• Development of selective IgM deficiency in systemic lupus erythematosus patients with disease of long duration.

  1987cited by this paper
• Immunoglobulin G (IgG) subclasses and human disease.

  1984cited by this paper
• Immunologic disorders in infants and children

  1973cited by this paper
• [Erythematosus].

  1971cited by this paper

• Serious infections and tuberculosis adversely impact outcomes of juvenile onset systemic lupus erythematosus in India

  2024cites this paper
• The mosaic of systemic lupus erythematosus: From autoimmunity to autoinflammation and immunodeficiency and back.

  2024cites this paper
• Reduced expressions of apoptosis-related proteins TRAIL, Bcl-2, and TNFR1 in NK cells of juvenile-onset systemic lupus erythematosus patients: relations with disease activity, nephritis, and neuropsychiatric involvement

  2024cites this paper
• Childhood-onset systemic lupus erythematosus associated with inborn errors of immunity: One or several conditions?

  2024cites this paper
• Lupus Nephritis in Children: Novel Perspectives

  2023cites this paper
• The yin and the yang of early classical pathway complement disorders.

  2022cites this paper
• Diagnostic Challenges in Patients with Inborn Errors of Immunity with Different Manifestations of Immune Dysregulation

  2022cites this paper
• Immunoglobulin levels in systemic lupus erythematosus: A narrative review

  2021cites this paper
• An Update on the Management of Childhood-Onset Systemic Lupus Erythematosus

  2021cites this paper
• Lupus manifestations in children with primary immunodeficiency diseases: Comprehensive phenotypic and genetic features and outcome

  2021cites this paper
• Lupus Nephritis

  2021cites this paper
• Acquired low immunoglobulin levels and risk of clinically relevant infection in adult patients with systemic lupus erythematosus: a cohort study.

  2020cites this paper
• Elevated serum interleukin-34 level in juvenile systemic lupus erythematosus and disease activity

  2020cites this paper
• Revisiting the complement system in systemic lupus erythematosus

  2020cites this paper
• Higher interferon score and normal complement levels may identify a distinct clinical subset in children with systemic lupus erythematosus

  2020cites this paper
• Alterations of Total Serum Immunoglobulin Concentrations in Pemphigus and Pemphigoid: Selected IgG2 Deficiency in Bullous Pemphigoid

  2020cites this paper
• Isotype defects

  2020cites this paper
• Mapping Out Autoimmunity Control in Primary Immune Regulatory Disorders.

  2020cites this paper
• Does Genetics Play a Role in Auto-immune Diseases?

  2020cites this paper
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  2018cites this paper
• Complement deficiency in pediatric-onset systemic lupus erythematosus

  2018cites this paper
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  2018cites this paper
• Selective IgA Deficiency

  2018cites this paper
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  2017cites this paper
• Complement in autoimmune diseases.

  2017cites this paper
• Approach to the Management of Autoimmunity in Primary Immunodeficiency

  2017cites this paper
• Management considerations for childhood-onset systemic lupus erythematosus patients and implications on therapy

  2016cites this paper
• High frequency of immunodeficiency-like states in systemic lupus erythematosus: a cross-sectional study in 300 consecutive patients.

  2016cites this paper
• Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical Pathway

  2016cites this paper
• C1q Deficiency and Neuropsychiatric Systemic Lupus Erythematosus

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• Primary immunodeficiency association with systemic lupus erythematosus: review of literature and lessons learned by the Rheumatology Division of a tertiary university hospital at São Paulo, Brazil.

  2016cites this paper
• Low C4, C4A and C4B gene copy numbers are stronger risk factors for juvenile-onset than for adult-onset systemic lupus erythematosus.

  2016cites this paper
• Systemic lupus erythematosus: Is it one disease?

  2016cites this paper
• Features of 847 Childhood‐Onset Systemic Lupus Erythematosus Patients in Three Age Groups at Diagnosis: A Brazilian Multicenter Study

  2016influential citation
• Rheumatologic manifestations of primary immunodeficiency diseases

  2016cites this paper
• Lupus eritematoso sistémico: ¿es una sola enfermedad?

  2016cites this paper
• Associação de imunodeficiência primária com lúpus eritematoso sistêmico: revisão da literatura e as lições aprendidas pela Divisão de Reumatologia de um hospital universitário terciário em São Paulo

  2016cites this paper
• utoimmune diseases and autoantibodies in ediatric patients and their first-degree relatives ith immunoglobulin A deficiency

  2015cites this paper
• Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus

  2015influential citation
• Cardiac tamponade as the initial presentation of systemic lupus erythematosus: a case report and review of the literature

  2015cites this paper
• Primary complement and antibody deficiencies in autoimmune rheumatologic diseases with juvenile onset: a prospective study at two centers

  2015cites this paper
• Early-Onset Autoimmune Disease as a Manifestation of Primary Immunodeficiency

  2015cites this paper
• A Multicenter Study of Invasive Fungal Infections in Patients with Childhood-onset Systemic Lupus Erythematosus

  2015cites this paper
• Clinical presentation of human C1q deficiency: How much of a lupus?

  2015cites this paper
• [Autoimmune diseases and autoantibodies in pediatric patients and their first-degree relatives with immunoglobulin A deficiency].

  2015cites this paper
• Doenças autoimunes e autoanticorpos em pacientes pediátricos e seus parentes de primeiro grau com deficiência de imunoglobulina

  2015cites this paper
• Cancer Immunology and Immunodeficiency TUMOR

  2015cites this paper
• Chapter 16 – Isotype Defects

  2014cites this paper
• Considerations for Primary Immune Deficiency Disorders in South America

  2014cites this paper
• Reduced expressions of Fas and Bcl-2 proteins in CD14+ monocytes and normal CD14 soluble levels in juvenile systemic lupus erythematosus

  2013cites this paper
• Attending to Warning Signs of Primary Immunodeficiency Diseases Across the Range of Clinical Practice

  2013cites this paper
• Pediatric Immunological Disorders Biorepository (PIDBioRep) at University of São Paulo Medical School, Brazil

  2013cites this paper
• Primary Immunodeficiency Diseases in Different Age Groups: A Report on 1,008 Cases from a Single Brazilian Reference Center

  2013cites this paper
• Hypogammaglobulinemia in pediatric systemic lupus erythematosus

  2013cites this paper
• The complement system in pediatric systemic lupus erythematosus, atypical hemolytic uremic syndrome, and complocentric membranoglomerulopathies

  2012cites this paper
• Taxonomy for systemic lupus erythematosus with onset before adulthood

  2012cites this paper
• Disseminated histoplasmosis in a juvenile lupus erythematosus patient.

  2012cites this paper
• Invasive Fungal Infections in Patients with Systemic Lupus Erythematosus

  2012cites this paper
• Complications of autologous hematopoietic stem cell transplantation for patients with autoimmune diseases

  2012cites this paper
• Defective and excessive immunities in pediatric diseases.

  2012cites this paper
• Increased neutrophil oxidative burst metabolism in systemic lupus erythematosus

  2012cites this paper
• Current world literature.

  2012cites this paper
• Advances in primary immunodeficiency diseases in Latin America: epidemiology, research, and perspectives

  2012cites this paper
• IgA deficiency: what is new?

  2012cites this paper