Results 1 to 10 of about 14,924 (223)

Management of hypogammaglobulinemia in pediatric patients with refractory lupus nephritis: a focus on belimumab [PDF]

open access: yesFrontiers in Pediatrics
BackgroundAlthough the use of belimumab in children with lupus nephritis (LN) has increased over the past few years, there are limited data on the safety of belimumab in such patients with hypogammaglobulinemia. There are scarce reports of an association
Yanan Han   +5 more
doaj   +2 more sources

Improving screening for antibody deficiency using calculated globulin and serum protein electrophoresis [PDF]

open access: yesFrontiers in Immunology
PurposeAntibody deficiencies, particularly Common Variable Immunodeficiency (CVID), represent a major health concern due to comorbidities linked to delayed diagnosis.
Linda Mokrane   +8 more
doaj   +2 more sources

Case report: Persistent hypogammaglobulinemia following hematopoietic stem cell transplantation from a sibling donor with heterozygous RAG1 mutation [PDF]

open access: yesFrontiers in Immunology
IntroductionHematopoietic stem cell transplantation (HSCT) is a curative treatment for pediatric hematologic and immunologic disorders, with successful immune reconstitution being critical for long-term survival.
Jing Wu   +3 more
doaj   +2 more sources

Calculated globulin as a surrogate marker for hypogammaglobulinemia: establishing clinical decision limits in a Brazilian population cohort [PDF]

open access: yesFrontiers in Immunology
IntroductionInborn errors of immunity (formerly primary immunodeficiencies) encompass a group of genetic disorders characterized by defects in innate and/or adaptive immunity.
André L. O. Feodrippe   +4 more
doaj   +2 more sources

CART CELL THERAPY BLACK SHADOW IN HEMATOLOGICAL DISORDERS : SYSTEMIC REVIEW WITH META-ANALYSIS

open access: yesHematology, Transfusion and Cell Therapy, 2022
Aim: To determine the effect of CART therapy on hypogammaglobulinemia and bone marrow aplasia, and to determine the probable medications in management of hypogammaglobulinemia with other associated risk factors and complications.
Ghada EL Gohary
doaj   +1 more source

Fresh-frozen plasma as a low-cost replacement of intravenous immunoglobulin for the treatment of symptomatic hypogammaglobulinemia

open access: yesJournal of Emergencies, Trauma and Shock, 2023
Hypogammaglobulinemia commonly presents with chronic diarrhea. Unfortunately, these patients require intravenous immunoglobulin (IVIG) transfusions of 400–800 mg/kg every 3–4 weeks as a standard treatment for hypogammaglobulinemia.
Pankaj Kumar   +4 more
doaj   +1 more source

A COVID-19 family cluster with retinitis pigmentosa and hypogammaglobulinemia

open access: yesAnnals of Thoracic Medicine, 2022
Hypogammaglobulinemia is a heterogeneous group of innate and acquired antibody deficiency with variable disease severity, recurrent pneumonia, and bronchiectasis.
Abeer N Alshukairi   +6 more
doaj   +1 more source

Humoral immune depression following autologous stem cell transplantation is a marker of prolonged response duration in patients with mantle cell lymphoma

open access: yesHaematologica, 2022
Rituximab maintenance (RM) after autologous stem cell transplantation (ASCT) is standard-of-care for young patients with mantle cell lymphoma (MCL). RM may enhance post-transplantation immune depression and risk of infections.
Louise Bouard   +13 more
doaj   +1 more source

Hypogammaglobulinemia following COVID-19 infection in a patient on maintenance rituximab

open access: yesSAGE Open Medical Case Reports, 2021
Hypogammaglobulinemia is a known side-effect of rituximab use. It is typically asymptomatic and transient, although certain factors, such as maintenance dosing and concomitant glucocorticoid use can lead to symptomatic or prolonged hypogammaglobulinemia.
Collin O’Bryan   +2 more
doaj   +1 more source

Clinical Courses of IKAROS and CTLA4 Deficiencies: A Systematic Literature Review and Retrospective Longitudinal Study

open access: yesFrontiers in Immunology, 2022
IKAROS and CTLA4 deficiencies are inborn errors of immunity and show similar clinical phenotypes, including hypogammaglobulinemia and autoimmune diseases (ADs).
Akihiro Hoshino   +30 more
doaj   +1 more source

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