Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID07590986

Identification of MPN-specific Antigens and Anti-MPN TCRs in Myeloproliferative Neoplasm

Led by Université Catholique de Louvain · Updated on 2026-05-15

150

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how the immune system responds to myeloproliferative neoplasms (MPN) in adults who have or are suspected to have MPN. This observational study aims to identify specific immune cells, called T cells, that can recognize MPN cells and to find targets on these cancer cells that may be useful for future immune-based treatments. The study focuses on adults with conditions like polycythemia vera, essential thrombocythemia, primary myelofibrosis, post-PMF, or unclassifiable MPN, and also includes healthy donors for comparison. Participants will provide blood and bone marrow samples, which researchers will analyze using laboratory methods including genetic sequencing, cell analysis, and cell culture experiments. These tests will help identify T cell receptors and tumor antigens linked to MPN cells. The study will continue for about 10 years to thoroughly monitor and identify these immune responses. During the study, participants will contribute samples that enable detailed research on immune cells and genetic material related to MPN. Researchers will measure the presence of MPN-specific CD8+ T cell clonotypes and their corresponding tumor antigens throughout the study period. Participants will not receive direct medical benefits, but their involvement will support the development of future immune-based therapies. The study will last approximately 10 years, allowing long-term observation and analysis.

CONDITIONS

Brief Title

Identification of MPN-specific Antigens and Anti-MPN TCRs in Myeloproliferative Neoplasm

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults previously diagnosed or suspected of having polycythemia vera, essential thrombocythemia, pre-primary myelofibrosis, overt primary myelofibrosis, or unclassifiable myeloproliferative neoplasm
  • Adults not previously diagnosed with a blood disorder can participate as controls
Not Eligible

You will not qualify if you...

  • Patients with any other hematological malignancy

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Approximately 10 years

Participants are observed over an extended period to identify specific immune responses related to myeloproliferative neoplasm.

Trial Site Locations

Total: 1 location

1

de Duve Institute, UCLouvain

Brussels, Woluwe, Belgium, 1200

Actively Recruiting

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Research Team

S

Sophie Lucas

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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