PubMed Health⌕ Search

PubMed · 3481426

IgG4 and hyposensitization.

Abstract

The mechanism of action of hyposensitization is still unclear. Probably, allergen-blocking antibodies have some effect, in particular in insect venom allergy, but it is likely that other mechanisms are operative as well. With the types of treatment currently available suppression of the production of specific IgE antibodies does not seem to be a dominating factor. In view of the presumed minor contribution of allergen-blocking antibodies in inhalant allergy, it is as yet impossible to define the role of IgG4 antibodies other than quantitatively: It is the main allergen-blocking antibody! There is no conclusive evidence that the IgG4 is the exclusive allergen-blocking antibody in immediate type allergy. However, its main biologic significance might well be on a completely different level, viz. prevention of immune complex disease. The production of non-complement fixing antibodies, unable to form large complexes due to functional monovalency, during prolonged antigenic exposure seems to provide adequate protection against complement-induced damage and other sequela of precipitating immune complexes that can be expected from a persistent production of IgG1. The rare occurrence of immune complex induced disorders during hyposensitization therapy is possibly a result of this phenomenon.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

S Van der Zee, R C Aalberse. IgG4 and hyposensitization.. https://doi.org/10.2500/108854187778999667

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Thermodynamic and kinetic analysis of the interaction between hepatitis B surface antibody and antigen on a gold electrode modified with cysteamine and colloidal gold via electrochemistry.

Hepatitis B surface antibody (HBsAb) was immobilized to the surface of a gold electrode modified with cysteamine and colloidal gold as matrices to detect hepatitis B surface antigen (HBsAg). Differential pulse voltammetry (DPV) method was used for the investigation of the specific interaction between the immobilized HBsAb and HBsAg in solution, which was followed as a change of peak current in DPV with time. With the modified gold electrode, the differences in affinity of HBsAb with HBsAg at the temperatures of 37 and 40 degrees C were easily distinguished and the kinetic rate constants (k(ass) and k(diss)) and kinetic affinity constant K were determined from the curves of current versus time. In addition, the thermodynamic constants, DeltaG, DeltaH and DeltaS, of the interaction at 37 degrees C were calculated, which were -56.65, -64.54 and -25.45 kJ mol(-1), respectively.

Antigen-Antibody Reactions↗

Impact of different inhibitor reactivities with commercial factor VIII concentrates on thrombin generation.

In order to describe the haemostatic role of a variation in inhibitor reactivity with different factor VIII (FVIII) concentrates, we have compared inhibitor titres against a panel of FVIII concentrates and correlated titre with the capacity to inhibit thrombin generation. Three plasma-derived concentrates were tested in vitro in mixing experiments with inhibitor plasmas from 11 patients with severe haemophilia A: Fanhdi, which contains von Willebrand factor (VWF) with a final ratio of approximately 1:1 (VWF IU per IU FVIII:C); Haemate-P with a ratio of 2.5:1 and Hemofil-M containing only trace amounts of VWF. In addition, the recombinant FVIII concentrate Kogenate Bayer containing no VWF was included. Inhibitor titres and the capacity to generate thrombin were measured. A statistically significant difference in measured titres was found with the highest titres recorded against Hemofil-M. The inhibitor titres needed to inhibit 50% maximum thrombin generation were the lowest for Kogenate Bayer and the highest and similar for Fanhdi and Haemate-P with intermediate titres needed for inhibition of Hemofil-M. In this study, the thrombin generation assay provides additional indications for the role of VWF in the treatment of patients with inhibitors. The VWF-containing concentrates Fanhdi and Haemate-P, added to FVIII-deficient plasma with the presence of inhibitor, generate more thrombin than do the purified concentrates Hemofil-M and Kogenate Bayer.

Antigen-Antibody Reactions↗