About this trial
When a person undergoes a stem cell transplant-an important procedure used to treat serious blood diseases such as leukaemia, lymphoma, or myeloma-the entire immune system is affected. The transplant essentially "resets" the immune system, meaning that the patient loses much of the protection against infections that has been built up over a lifetime. After the transplant, the patient therefore needs to be revaccinated against several diseases, such as tetanus, diphtheria, polio, COVID-19, and pneumococcal disease.
In this study, we aim to investigate how B cells-the immune cells that produce antibodies-reconstitute after a stem cell transplant. We are particularly interested in a genetic process called VDJ recombination, through which each B cell develops a unique receptor that enables it to recognize and fight a specific virus or bacterium. This process is what makes our immune system so effective. But what happens to this diversity after the entire immune system has been restarted with new stem cells? Does the body regain the same ability to recognize pathogens? Are there differences between patients who receive their own stem cells (autologous transplantation) and those who receive stem cells from another person (allogeneic transplantation)?
To answer these questions, we will follow patients undergoing stem cell transplantation at Umeå University Hospital. We will collect blood samples before and after the transplantation and will assess whether-and how well-patients generate antibodies in response to the vaccines given after transplantation. Using flow cytometry and genetic analyses, we will examine both which B-cell populations are generated and what their genetic architecture looks like. The goal is to understand how the new immune system is rebuilt after transplantation and, ultimately, to help improve vaccination strategies and infection prevention for this vulnerable patient group
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age > 18 years.
Willing and able to participate in all parts of the study.
Signed written consent.
Patients with a plasma cell disease of lymphoma that qualify for autologous hematological stem cell transplantation determined by the attending physician OR Patients with a condition for which allogenic stem cell transplantation could be needed and qualify for haematological stem cell transplantation according to the attending physician OR Stem cell donor, donating to a study participant.
Disqualifiers
Unable to give informed consent.
Not suitable for participation in the study according to the view of the attending physician.
Previous participation in this trial.
Trial population
Patients who fulfill the inclusion criteria and will receive their stem cell transplantation at the department of hematology at the Umeå university hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
VDJ recombination of the B-cell receptor (BCR) after autologous and allogenic stem cell transplantation compared to samples from before transplantation or to samples from stem cell donor. For comparison IgM and IgG antibody levels will also be measured.
The study will examine the BCR development and VDJ recombination after stem cell transplantation in response to exposure to different vaccine antigens compared to the samples taken before transplantation or samples from the stem cell donor when available. Because the lack of previous studies and by being an exploratory study it is not possible to define quantitative measurable endpoints.
Differences in response to vaccine antigens following autologous stem cell transplantation compared to allogenic stem cell transplantation in VDJ recombination of the B-cell receptor and in IgM and IgG antibody levels.
The study will examine the BCR development and VDJ recombination after stem cell transplantation in response to exposure to vaccine antigens compared to the before transplantation or to the stem cell donor. Because the lack of previous studies and by being an exploratory study it is not possible to define quantitative measurable endpoints..
Sponsors and contacts
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Umeå University
Lead sponsor
Region Västerbotten
Collaborator
This trial is not recruiting at the moment. You can still explore other options: