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RNAi-mediated Double Gene Knockdown and Gustatory Perception Measurement in Honey Bees Apis mellifera
Published on: July 25, 2013
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Combined active and passive immunotherapy in honeybee-sting allergy
The Journal of Allergy and Clinical Immunology
|July 1, 1986
Summary
Passive immunotherapy with beekeeper gammaglobulin temporarily increased tolerated honeybee venom doses in allergic patients. However, allergic side effects recurred, suggesting limitations in the patients' own IgG response for long-term bee venom immunotherapy.
Area of Science:
- Allergy and Immunology
- Immunotherapy
- Toxicology
Background:
- Bee venom immunotherapy (VIT) is a treatment for honeybee sting allergies.
- Previous attempts at VIT were halted due to recurrent allergic side effects (SE).
- Passive immunotherapy using beekeeper gammaglobulin was explored to improve VIT tolerance.
Purpose of the Study:
- To evaluate the efficacy of beekeeper gammaglobulin pretreatment in patients with honeybee sting allergy previously intolerant to VIT.
- To assess the impact of passive immunotherapy on the dose escalation and maintenance of bee venom immunotherapy.
- To investigate the qualitative aspects of the patients' IgG response to bee venom components.
Main Methods:
- Five patients with a history of severe allergic side effects to bee venom immunotherapy (VIT) received pretreatment with beekeeper gammaglobulin.
- Rush hyposensitization protocol was used to increase the tolerated dose of honeybee venom (BV).
- Immunological analysis, including crossed radioimmunoelectrophoresis and IgG subclass analysis, was performed.
Main Results:
- Pretreatment with beekeeper gammaglobulin allowed a 5- to 800-fold increase in tolerated bee venom dose, with maintenance doses reached rapidly.
- The IgG response to bee venom was not suppressed by the gammaglobulin infusion.
- Allergic side effects recurred in all patients within 2 to 9 weeks, necessitating dose adjustments or discontinuation in one case.
- Analysis revealed a lack of IgG response to specific bee venom components in some patients and an atypical IgG subclass pattern compared to tolerant beekeepers (lacking IgG2 response).
Conclusions:
- Beekeeper gammaglobulin can facilitate dose escalation in bee venom immunotherapy for allergic patients.
- The recurrence of side effects suggests that passive immunotherapy does not fully resolve underlying immune system deficiencies.
- Qualitative defects in the patients' endogenous IgG response, particularly the absence of an IgG2 response, may contribute to treatment failure in bee venom immunotherapy.
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