Role of T Lymphocytes in Hypersensitivity Reactions to Asparaginase in Patients Treated for Acute Lymphoblastic Leukemia.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-99
SponsorCentre Hospitalier Universitaire de Nice

About this trial

Acute lymphoblastic leukemia is a type of blood cancer that primarily affects children. Fortunately, current treatments are highly effective. One of the key drugs used is asparaginase, which works by depriving leukemic cells of a substance that is essential for their survival.

However, asparaginase can also cause adverse effects, including severe allergic reactions in some patients. These reactions may be related to specific genetic factors and/or individual differences in immune responses.

The aim of this research project is to better understand why certain patients develop poor tolerance to asparaginase. To achieve this, the investigators plan to collect blood cells from patients during treatment and then re-expose these cells to the drug in the laboratory. the investigators will assess whether specific immune cells-particularly T lymphocytes-become abnormally activated, which could help explain hypersensitivity reactions.

Ultimately, our goal is to develop a biological assay capable of predicting which patients are at increased risk of reacting adversely to asparaginase, so that they can be offered a more tailored and safer treatment strategy.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Confirmed diagnosis of B- or T-lineage acute lymphoblastic leukemia (ALL) according to current morphological, immunophenotypic, and molecular criteria.

Treatment according to a standard therapeutic protocol including administration of asparaginase (PEG-asparaginase or native E. coli asparaginase).

Age ≥ 1 year.

Inclusion prior to the consolidation phase (sampling scheduled between induction and consolidation).

Disqualifiers

Prior hematopoietic stem cell transplantation (HSCT).

Trisomy 21 (Down syndrome), due to distinct immunological features and potentially different tolerance to asparaginase.

Emergency situation or clinical context not allowing appropriate patient information and informed consent.

Trial design

Design model

Single group

Treatments tested in this trial

  • Asparaginase-induced in vitro T-cell stimulation

    Drug

    Flow cytometric analysis of asparaginase-specific T-cell activation, compared with an unstimulated control condition and a non-antigen-dependent (polyclonal) stimulation condition. Comparison of asparaginase-specific T-cell activation between patients who developed a clinical reaction to asparaginase and patients who did not.

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: In vitro exposure to asparaginaseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of T lymphocytes producing IFN-γ in response to asparaginase stimulation, compared with background (unstimulated) levels and the maximal response induced by PMA/ionomycin within the same patient.

Absolute number of T lymphocytes producing IFN-? in response to asparaginase stimulation

Time frame
At inclusion (baseline) day 1

Secondary outcomes

Other outcomes

Sponsors and contacts

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