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Regulation of Blood Dendritic Cells During Immune Therapy for Hymenoptera Venom Allergy

Regulation of Blood Dendritic Cells During Immune Therapy for Hymenoptera Venom Allergy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00947908
Enrollment
20
Registered
2009-07-28
Start date
2009-06-30
Completion date
2010-06-30
Last updated
2010-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hymenoptera Venom Allergy

Keywords

Hymenoptera venom allergy, Dendritic cells (DC)

Brief summary

Dendritic cells (DC) play a key role in the pathogenesis of allergic diseases. The regulation of blood dendritic cells in patients with hymenoptera venom allergy before and during immune therapy is unknown.

Interventions

BIOLOGICALHymenoptera venom

Patients are treated with hymenoptera (bee or wasp) venom using subcutaneous injections. The initiation of immune therapy consists of a 52-hour-period in which patients are treated with increasing doses of hymenoptera venom. Afterwards, patients are treated with monthly subcutaneous injections with a fixed dose of hymenoptera venom. Blood will be collected directly before and 1 hour after initiation of immune therapy and after 12 months of immune therapy (directly before the next subcutaneous injection of hymenoptera venom).

Sponsors

University of Rostock
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with diagnosed hymenoptera venom allergy * No previous treatments for hymenoptera venom allergy

Exclusion criteria

* Treatment with immunosuppressive agents * Any malignant disease * Infections within 1 week prior to the initiation of the treatment

Design outcomes

Primary

MeasureTime frame
Number of myeloid DC and plasmacytoid DC in peripheral bloodDirectly before, 1 hour after, and 12 months after initiation of immune therapy

Secondary

MeasureTime frame
Surface molecule expression on myeloid DC and plasmacytoid DCDirectly before, 1 hour after, and 12 months after initiation of immune therapy

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026