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Screening potential allergy vaccine components

In vitro evaluation of the immune-skewing potential of different candidate building blocks for nanoparticle-based allergen immunotherapy for treatment of allergy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24623
Enrollment
50
Registered
2020-01-13
Start date
2020-01-31
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Allergy

Interventions

None

Sponsors

Investigator initiated- Amsterdam university medical centers
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: There are three categories of subjects for blood donation: ? Subjects with doctor-diagnosed allergic rhinitis ? Subjects with doctor-diagnosed non-allergic rhinitis ? Healthy subjects, defined as not having allergic or non-allergic rhinitis or other inflammatory non-communicable diseases such as rheumatoid arthritis, type 2 diabetes, celiac disease, colitis ulcerosa, Chrohn’s disease, and multiple sclerosis. All three categories should meet the following additional criteria: • Age between 18 and 65. • Signed informed consent.

Exclusion criteria

Exclusion criteria: • History of AIT (SCIT or SLIT) with any allergen within the past year at the time of blood donation. • Ongoing AIT (SCIT or SLIT) with any allergen at the time of blood donation. • Vaccination within one week before blood donation. • Immunosuppressive or biological medication (e.g. IL-5, anti-IgE therapy) within the last six months prior to blood donation. • Severe immune disorders (including auto-immune diseases) and/or diseases requiring immunosuppressive drugs. • Active malignancies or any malignant disease during the previous 5 years. • Active inflammation or infection at the time of blood donation. • Use of systemic steroids within 4 weeks before the blood donation. • Treatment with systemic and local ß-blockers. • Subjects who are students or employees of the institution or 1st grade relatives or partners of the investigators.

Design outcomes

Primary

MeasureTime frame
The aim of the study is to obtain a blood sample for isolation of monocytes. These monocytes will be used to generate monocyte-derived dendritic cells (moDC).

Contacts

Public ContactLaurian Jongejan

Amsterdam university Medical centers

l.zuidmeer@amsterdamumc.nl0205666819

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)