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NCT Number: NCT06195800

Biomarkers of aHSCT

The underlying disease mechanisms which occur in patients with immune mediation neurological diseases, such as Multiple Sclerosis (MS), are incompletely understood. For such patients, autologous haematopoietic stem cell transplantation (aHSCT) has been increasingly used as a highly successful one-off treatment for some patients. This treatment aims to delete the faulty immune system with a course of chemotherapy and then 'reboot' the immune system using a patients' own stem cells (a cell with the unique ability of being a building block to create many different cells in the body) to stop further damage. Over the last 20 years more than 1800 patients with MS have been treated in Europe with high levels of success. It may be more successful than disease modifying treatment but unfortunately, a small portion of people do not respond to this treatment optimally and continue to accumulate disability. There is a risk of side effects, restricted largely to the time of treatment, which necessitates the need to ensure appropriate patients are treated. Whilst aHSCT is a very effective therapy, it is still in its early phase of development, is not in widespread use, and there is incomplete knowledge regarding how it works and importantly, why it does not work in some patients, and how to monitor response to treatment.

Unfortunately, there is no way of detecting which patients will, and will not, benefit from the different treatments available or a way of monitoring the immune system to ensure further treatment is provided before irreversible damage occurs.

This study will investigate the immune system which is found in the fluid surrounding the brain and spinal cord, blood and stool of patients undergoing aHSCT and compare it to those receiving disease modifying treatment. This study will therefore further the understanding of biomarkers of aHSCT to develop an awareness of how it can be refined, may improve monitoring of patients following treatment and permit the development of markers which can predict potential treatment success or failure before patients are exposed to the risks.

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Sheffield Teaching Hospitals NHS Foundation Trust

Sheffield, England, S10 2JF, United Kingdom

Location status: Recruiting

Location contact

Gavin Brittain, MBBS, MRCP

CONTACT

[email protected]

07845519027

Gavin Brittain, MBBS, MRCP

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of a immune mediated neurological disease according to disease specific criteria (active treatment arm) or diagnosis of relapsing remitting multiple sclerosis (control arm).
  • Treatment with autologous haematopoetic stem cell transplantation (active treatment arm) or high efficacy disease modifying treatment (control arm).
  • Willing to provide biological samples for analysis and undergo clinical assessments for the duration of follow up.
  • Able to understand English and provide informed consent.

Exclusion criteria

  • Inability to provide informed consent.

Treatment and study plan

Primary outcomes

  1. Quantitatively and qualitatively characterise the immune profile of the stem cells, blood, cerebrospinal fluid (CSF) and the microbiome pre and post treatment.

    Time frame: 24 months

    Phenotype profiling of stem cells, cells in blood and CSF using multi-parameter flow cytometry.

    Profile the gut microbiome using 16S rRNA sequencing and flow cytometric analysis.

  2. Perform single cell RNA sequencing (scRNA-Seq) on paired CSF and blood pre and post treatment.

    Time frame: 24 months

    Profiling of T cell receptor and B cell receptor repertoire diversity and clonality

Secondary outcomes

  1. Characterisation of the regeneration of mucosal cell immunity and the reconstitution of pathogen specific immunity following aHSCT by scRNA-Seq on nasopharyngeal swabs and mucosal strips.

    Time frame: 24 months

    Assess immune response in treated patients post vaccination.

  2. Evaluate immunological disease response and the duration of response to aHSCT according to expanded disability status scale score (EDSS)

    Time frame: 24 months

    EDSS to be observed longitudinally following treatment.

  3. Evaluate immunological disease response and the duration of response to aHSCT according to low contrast visual acuity (LCLA)

    Time frame: 24 months

    LCLA to be observed longitudinally following treatment.

  4. Evaluate immunological disease response and the duration of response to aHSCT according to multiple sclerosis functional composite score (MSFC)

    Time frame: 24 months

    MSFC to be observed longitudinally following treatment.

  5. Evaluate immunological disease response and the duration of response to aHSCT according to short form 36 (SF-36)

    Time frame: 24 months

    SF-36 to be observed longitudinally following treatment.

  6. Evaluate immunological disease response and the duration of response to aHSCT according to symbol digit modality test (SDMT)

    Time frame: 24 months

    SDMT to be observed longitudinally following treatment.

  7. Evaluate immunological disease response and the duration of response to aHSCT according to Karnofsky performance status

    Time frame: 24 months

    Karnofsky performance status to be observed longitudinally following treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

Gavin Brittain, MBBS, MRCP

CONTACT

[email protected]

+44114 271 1900

Sponsors and collaborators

Lead sponsor

Sheffield Teaching Hospitals NHS Foundation Trust

Other

Collaborators

  • Nottingham Trent University
  • Sheffield Hospitals Charity
  • University of Sheffield

Registry information

Official study title

Identifying Immune Biomarkers of Disease and Disease Control in Autoimmune Neurological Disease Using Autologous Haematopoietic Stem Cell Transplantation

Acronym: BIO-MS

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jan 8, 2024
Registry last updated
Jan 8, 2024

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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