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Researching trained immunity in ANCA-associated vasculitis

Researching trained immunity in ANCA-associated vasculitis - TACTIC-AAV

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53213
Enrollment
100
Registered
2023-06-26
Start date
2024-06-11
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

AAV ANCA-associated vasculitis Wegner

Interventions

None listed

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age between 18 and 70 years old. Positive AAV diagnosis.

Exclusion criteria

Exclusion criteria: Lack of informed consent Current infection CKD stage 5 or dialysis Pregnancy Active cancer

Design outcomes

Primary

MeasureTime frame
1. What are the differences in the transcriptome of circulating monocytes from AAV patients when the disease is in remission or when the disease is active (flares), and how does this differ with the transcriptome of circulating monocytes from healthy individuals? 2. What are the differences in the epigenome of circulating monocytes from AAV patients when the disease is in remission or when the disease is active (flares), and how does this differ with the epigenome of circulating monocytes from healthy individuals? 3. What are the differences in the cytokine response of circulating monocytes from AAV patients when the disease is in remission or when the disease is active (flares), and how does this differ with the response of circulating monocytes from healthy individuals?

Secondary

MeasureTime frame
1. Are there correlations between the trained immunity profile of circulating monocytes (identified by transcriptome, epigenetics, and cytokine response) and the degree of current disease activity in clinical variables of AAV patients? 2. Are there correlations between the trained immunity profile of circulating monocytes (identified on the basis of the transcriptome, epigenetics, and cytokine response) and the risk of the occurrence of flares in the future. 3. Are there correlations between the trained immunity profile of circulating monocytes (identified based on the transcriptome, epigenetics, and cytokine response) and inflammatory markers in the blood.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)