Actively Recruiting

Age: 18Years +
All Genders
ID06458504

Virus-induced Immunosuppression Via Infection of Hematopoietic Progenitors

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-03-20

45

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research explores how HIV-1 and SARS-CoV-2 viruses may infect long-lived hematopoietic stem and progenitor cells (HSPCs) that have the ability to renew themselves. These infected cells could become a lasting source of infected cells, affecting the process of blood cell formation known as hematopoiesis. The study aims to understand virus-induced immunosuppression, a condition where immune cells decline due to viral infections, which is serious and seen in chronic HIV-1 and some COVID-19 patients. The mechanisms behind this immunosuppression and effective treatments are not well known. The study will evaluate which types of HSPCs are targeted by HIV-1 and SARS-CoV-2, both inside the body and in laboratory settings. It will also assess whether infected HSPCs change the bone marrow environment by increasing inflammatory signals that could harm the production of lymphocytes, a type of immune cell. This observational study does not involve treatments but focuses on detailed evaluations. Participants include HIV-positive patients with various viral loads and healthy individuals who have had bone marrow biopsies or myelograms as part of their medical care at Ambroise Paré Hospital. Researchers will monitor the bone marrow environment over a year to see how infected cells may affect it. Various tests and analyses will be performed to measure immune status and bone marrow changes throughout the study until its completion in March 2026.

CONDITIONS

Brief Title

Viral Infection of HSPC Impacts Hematopoiesis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • HIV-positive patients with either negative or positive viral load
  • Managed at Ambroise Paré Hospital
  • Patients with a bone marrow biopsy or myelogram performed as part of their care
  • Healthy subjects without HIV who have had a bone marrow biopsy or myelogram for suspected hematological issues
  • Managed at Ambroise Paré Hospital
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

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.

Sample Collection

Duration - Up to 1 year

Participants provide bone marrow biopsies or myelograms as part of their routine care for evaluation of hematopoietic stem and progenitor cells (HSPC) infection.

1 to 2 visits depending on clinical care

Long-term Monitoring

Duration - Up to 1 year

Participants are monitored for changes in the bone marrow environment and immune cell function over time.

Trial Site Locations

Total: 1 location

1

Hematology and interne medicine department, Ambroise Paré hospital - APHP

Boulogne-Billancourt, France, 92100

Actively Recruiting

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Research Team

C

Claude CAPRON, MD, PhD

F

Fernando REAL, PhD

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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