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Related Concept Videos

Humoral Immune Responses01:36

Humoral Immune Responses

Overview
Transcytosis of IgG01:15

Transcytosis of IgG

Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
Hypersensitivity Reactions: Cytolytic Reactions01:01

Hypersensitivity Reactions: Cytolytic Reactions

Type II hypersensitivity involves IgG and IgM antibodies targeting cell surface antigens, leading to cell destruction. This can occur through complement activation, antibody-dependent cell-mediated cytotoxicity (ADCC), or acting as opsonins for phagocytosis. When excessive, these reactions cause significant tissue damage.Drug-induced hemolytic anemia is a common example, where drugs like penicillin or cephalosporins bind to red blood cells, forming drug-protein complexes. These complexes...
Hypersensitivity Reactions: Immune-Complex Reactions01:19

Hypersensitivity Reactions: Immune-Complex Reactions

Type III hypersensitivity reactions occur when antigen–antibody complexes form and activate the complement system. Normally, these complexes help the clearance of antigens by phagocytes and red blood cells. However, when large numbers of immune complexes are present, they can deposit in tissues—particularly in the walls of blood vessels—leading to inflammation and tissue injury. These deposits trigger complement activation and neutrophil recruitment, resulting in serum sickness, a systemic...
Immunodeficiency Diseases01:25

Immunodeficiency Diseases

Immunodeficiency disorders are conditions in which the immune system's ability to fight infectious disease and cancer is compromised or entirely absent. The immune system comprises a complex network of cells, tissues, and organs that work together to protect the body from potentially harmful invaders. When this system is deficient or not functioning properly, it leaves the body susceptible to infections, diseases, or other complications.
There are three main causes of immunodeficiency disorders...

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Related Experiment Video

Updated: Jul 9, 2026

Generation of Recombinant Human IgG Monoclonal Antibodies from Immortalized Sorted B Cells
10:32

Generation of Recombinant Human IgG Monoclonal Antibodies from Immortalized Sorted B Cells

Published on: June 5, 2015

Reversible hypogammaglobulinaemia.

I M E Desar1, C M R Weemaes, M van Deuren

  • 1Department of General Internal Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.

The Netherlands Journal of Medicine
|December 7, 2007
PubMed
Summary

Recovery from hypogammaglobulinaemia is rare but possible. This study highlights spontaneous immunoglobulin restoration in three patients and suggests testing antibody responses after stopping immunoglobulin substitution.

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Last Updated: Jul 9, 2026

Generation of Recombinant Human IgG Monoclonal Antibodies from Immortalized Sorted B Cells
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Area of Science:

  • Immunology
  • Clinical Medicine

Background:

  • Hypogammaglobulinaemia, a condition of low immunoglobulin levels, often necessitates long-term immunoglobulin substitution therapy.
  • Understanding potential recovery mechanisms is crucial for optimizing patient management.

Observation:

  • Four patients requiring prolonged immunoglobulin substitution for hypogammaglobulinaemia were studied.
  • One patient had systemic lupus erythematosus (SLE), while three had primary hypogammaglobulinaemia of unknown etiology.
  • All patients exhibited IgA deficiency, persisting even after recovery of IgG and IgM production.

Findings:

  • Spontaneous recovery of immunoglobulin production was observed in three patients without known cause.
  • Cessation of azathioprine therapy might have contributed to recovery in the SLE patient.
  • Two patients with anti-IgA antibodies resumed producing them after discontinuing immunoglobulin therapy.

Implications:

  • Reversible hypogammaglobulinaemia, though uncommon, can occur.
  • Discontinuation of immunoglobulin substitution and assessment of vaccine response are recommended when recovery is suspected.