Immunoglobulin G4-Related Disease

Immunoglobulin G4-related disease is a spectrum of systemic autoimmune diseases in which immunoglobulin G4 plays a pathophysiologic role. It can affect multiple organs in highly variable presentations, characterized by inflammatory lesions composed of IgG4-positive plasma cells, further infiltrated by T helper cells when linked to progressive fibrosis and eventual organ damage. Discover the latest research on immunoglobulin G4-related disease here.

June 12, 2020
Open Access

IgG4-Related Disease with Selective Testicular Involvement- A Rare Entity: Case Report with Review of Literature

Türk patoloji dergisi
Asbah ShamsPuneet Gupta
July 4, 2020

Autoimmune pancreatitis type 2

Current Opinion in Gastroenterology
Nicolò de Pretis, Luca Frulloni
May 19, 2020
Case Report

Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis

Translational Andrology and Urology
Young Jin KimEun Hui Bae
June 12, 2020

Immunological Role of IgG Subclasses

Immunological Investigations
Cecilia NapodanoUmberto Basile
April 7, 2020

Pulmonary Eosinophilic Granulomatosis with Polyangiitis Has IgG4 Plasma Cells and Immunoregulatory Features

The American Journal of Pathology
Zachary M DongFrederic Clayton
June 23, 2020

Coexistence of IgG4-related autoimmune hepatitis and inflammatory pseudotumors of the liver:a case report

Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology
Yasuyo AdachiTakao Endo
July 7, 2020

Efficacy and limitations of the histological diagnosis of type 1 autoimmune pancreatitis with endoscopic ultrasound-guided fine needle biopsy with large tissue amounts

Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [et Al.]
Kenji NotoharaKazuichi Okazaki
March 25, 2020
Review

IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review

Rheumatology International
Shota OkamotoTakayuki Sumida
March 28, 2020
Case Report

Orbital pseudotumor as the presenting symptom of Crohn's disease in a male child

American Journal of Ophthalmology Case Reports
Rhys IshiharaRichard Legge
April 30, 2020

IgG4-related disease: a clinical perspective

Rheumatology
Federica MaritatiAugusto Vaglio
April 15, 2020

Divergent chemokine receptor expression and the consequence for human IgG4 B cell responses

European Journal of Immunology
Peter-Paul A UngerTheo Rispens
May 28, 2020

Immunostaining With Immunoglobulin G Subclass Antibody Cocktail for Diagnosis of Type 1 Autoimmune Pancreatitis

International Journal of Surgical Pathology
Rie NakataHiroyoshi Ota
June 18, 2020
Review
Open Access

Autoimmune Pathology in Myasthenia Gravis Disease Subtypes Is Governed by Divergent Mechanisms of Immunopathology

Frontiers in Immunology
Miriam L FichtnerKevin C O'Connor
April 13, 2020

Thoracic Involvement in IgG4-Related Disease

Seminars in Respiratory and Critical Care Medicine
Marta Casal MouraJay H Ryu

Sign up to follow this feed and discover related papers.

Related Feeds

Acute Disseminated Encephalomyelitis

Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disease of the central nervous system. Discover the latest research on acute disseminated encephalomyelitis here.

Addison Disease

Addison's disease, also known as primary adrenal insufficiency and hypocortisolism, is a long-term endocrine disorder in which the adrenal glands do not produce enough steroid hormones. Discover the latest research on Addison's disease here.

Adult-Onset Still's Disease

Adult-onset Still's disease (AOSD) is a form of Still's disease, a rare systemic autoinflammatory disease characterized by the classic triad of persistent high spiking fevers, joint pain, and a distinctive salmon-colored bumpy rash. Discover the latest research on AOSD here.

Anti-N-Methyl-D-Aspartate Receptor Encephalitis

Anti-N-Methyl-D-Aspartate (NMDA) receptor encephalitis is a form of of brain inflammation due to antibodies against NMDA receptors. Discover the latest research on anti-NMDA receptor encephalitis here.

Antiphospholipid Syndrome

Antiphospholipid syndrome or antiphospholipid antibody syndrome (APS or APLS), is an autoimmune, hypercoagulable state caused by the presence of antibodies directed against phospholipids.

Autoimmune Diabetes & Tolerance

Patients with type I diabetes lack insulin-producing beta cells due to the loss of immunological tolerance and autoimmune disease. Discover the latest research on targeting tolerance to prevent diabetes.

Autoimmune Disease Therapy

In autoimmune diseases, the immune system responds and attacks self-antigens and damages or impairs the function of the tissues. The treatment for autoimmune diseases often involves immunosuppressive agents, but newer treatments are being investigated. Discover the latest research on autoimmune disease therapy here.

Autoimmune Diseases

Autoimmune diseases occur as a result of an attack by the immune system on the body’s own tissues resulting in damage and dysfunction. There are different types of autoimmune diseases, in which there is a complex and unknown interaction between genetics and the environment. Discover the latest research on autoimmune diseases here.

Autoimmune Hemolytic Anemia

Autoimmune hemolytic anemia (AIHA) occurs when antibodies directed against the person's own red blood cells (RBCs) cause them to burst (lyse), leading to an insufficient number of oxygen-carrying red blood cells in the circulation. Discover the latest research on AIHA here.

Autoimmune Hepatitis

Autoimmune hepatitis formerly called lupoid hepatitis, is a chronic, autoimmune disease of the liver that occurs when the body's immune system attacks liver cells causing the liver to be inflamed. Discover the latest research on autoimmune hepatitis here.

© 2020 Meta ULC. All rights reserved
/feed-previews/immunoglobulin-g4-related-disease/ba889a87-013e-4b06-bef5-e99848ec6bb9