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Completed

NCT Number: NCT04453917

Dynamics of T Cell Expression of Immune Checkpoint Molecules in Progressive Multifocal Leukoencephalopathy

Progressive multifocal leukoencephalopathy (PML) is a rare viral infection of the central nervous system (CNS) occurring in immunocompromised patients. Recovery of JC virus (JCV) specific T cell immune responses is the only available therapeutic option. JCV may use immune checkpoint inhibitory pathways to evade immune responses. The aim of this project is to determine whether T cell expression of immune checkpoint molecules is correlated to antiviral T cell responses, control of JCV replication and PML outcome. Immune checkpoint blockade by reversing T cell exhaustion may represent a therapeutic perspective for PML.

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Key information

About this study

PML is a devastating orphan disease of the CNS due to the reactivation of JCV in immunocompromised patients. Given the lack of drugs controlling JCV replication, initiation of antiretroviral therapy in HIV-infected patients or cessation of immunosuppressive therapies in others, and subsequent recovery of JCV-specific T cell immune responses remains to date the only available therapeutic option. Promoting antiviral immune responses may improve the control of viral replication and the outcome of this severe disease. Immune checkpoint molecules such as PD-1 are inhibitory receptors expressed on T cells that trigger inhibitory signaling pathways, limiting effector immune responses in cancer and chronic infections. Immune checkpoint inhibitory pathways implicated in evading immune responses may be at play in PML. Immune checkpoint blockade using monoclonal antibodies targeting PD-1, by reversing T cell exhaustion, has been suggested as a therapeutic perspective for PML. More insights in the dynamics of immune checkpoint molecules expressed by T cells in PML patients are needed to pave the way for a therapeutic study.

The aim here is to determine whether T cell expression of a broad range of immune checkpoint molecules, and its dynamics, correlates with the generation of antiviral of immune responses, the control of JCV replication and PML outcome.

To this end the investigators will recruit 15 PML patients from 4 teaching hospitals in the South West of France and assess at PML diagnosis and 1, 3 and 6 months after, the expression of immune checkpoint molecules on circulating T cells, ex vivo specific immune responses against a JCV peptide library, JC viral load in cerebrospinal fluid, blood and urine, and clinical and neuroradiological outcomes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults ≥18 years old
  • Informed consent
  • Active virological PML : Recent neurological symptoms (< 3 months) with brain MRI lesions suggestive of PML and positive PCR in cerebrospinal fluid for JCV
  • Affiliated or benefiting from public health insurance.

Exclusion criteria

  • Non active PML
  • Possible PML with negative JCV PCR
  • Adults under guardianship or other legal protection, deprived of their liberty by judicial or administrative decision
  • Pregnant and/or breastfeeding women

Treatment and study plan

collection of blood and urine

Biological

Collection of blood (47 mL) and urine (5 mL) at PML diagnosis and 1, 3 and 6 months after, for analysis of immune checkpoint molecules expression, detection of antiviral immune responses and virological analyses.

Spinal tap

Biological

Spinal tap for monitoring of JC viral load at PML diagnosis and 1, 3 and 6 months after, and collection of CSF (2 mL) for virological analyses.

Brain MRI

Diagnostic Test

Brain MRI at at PML diagnosis and 3 and 6 months after

Neurological evaluation

Biological

Neurological evaluation at PML diagnosis and 1, 3 and 6 months after

Primary outcomes

  1. Immune checkpoint molecules

    Time frame: 1 month

    Expression level of a broad panel of immune checkpoint molecules by T cells at PML diagnosis bu flow cytometry

  2. Immune checkpoint molecules

    Time frame: 3 months

    Expression level of a broad panel of immune checkpoint molecules by T cells at PML diagnosis bu flow cytometry

  3. Immune checkpoint molecules

    Time frame: 6 months

    Expression level of a broad panel of immune checkpoint molecules by T cells at PML diagnosis bu flow cytometry

  4. JC viral load

    Time frame: 1 month

    JC viral load in cerebrospinal fluid, blood and urine by ultra-sensitive PCR at PML diagnosis

  5. JC viral load

    Time frame: 3 months

    JC viral load in cerebrospinal fluid, blood and urine by ultra-sensitive PCR at PML diagnosis

  6. JC viral load

    Time frame: 6 months

    JC viral load in cerebrospinal fluid, blood and urine by ultra-sensitive PCR at PML diagnosis

  7. Detection of immune responses against a JCV peptide library

    Time frame: 1 month

    Detection of specific immune responses against a JCV peptide library at PML diagnosis by flow cytometry

  8. Detection of immune responses against a JCV peptide library

    Time frame: 3 months

    Detection of specific immune responses against a JCV peptide library at PML diagnosis by flow cytometry

  9. Detection of immune responses against a JCV peptide library

    Time frame: 6 months

    Detection of specific immune responses against a JCV peptide library at PML diagnosis by flow cytometry

Secondary outcomes

  1. Differential impact of immune checkpoint inhibition

    Time frame: 1 month, 3 months and 6 months

    Differential impact of immune checkpoint inhibition in vitro on detection of specific immune responses at PML diagnosis by flow cytometry

  2. Clinical outcome with Performance status

    Time frame: 1 month, 3 months and 6 months

    Clinical outcome using validated scales such as Performance status at PML diagnosis

  3. Clinical outcome with NIHSS

    Time frame: 1 month, 3 months and 6 months

    Clinical outcome using validated scales such as NIHSS (National Institute of Health Stroke Score) at PML diagnosis

  4. Clinical outcome with Rankin

    Time frame: 1 month, 3 months and 6 months

    Clinical outcome using validated scales such as Rankin at PML diagnosis

  5. Neuroradiological monitoring

    Time frame: 3 months and 6 months

    Neuroradiological monitoring by brain MRI at PML diagnosis

  6. JC virus genotyping

    Time frame: 1 month, 3 months and 6 months

    JC virus genotyping in blood, cerebrospinal fluid (CSF) and urine by ultra-sensitive PCR at PML diagnosis

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Registry information

Acronym: ICIP

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Jul 1, 2020
Registry last updated
Dec 31, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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