Quantification of Peripheral Blood iNKTs After Allogeneic Stem Cell Transplantation (QiNKT-HSCT)
Standardised Quantification of Invariant NKT Cells Using DryTube Technology and Flow Cytometry in Patients Who Have Undergone Allogeneic Haematopoietic Stem Cell Transplantation.
調査の概要
詳細な説明
Allogeneic haematopoietic stem cell transplantation (HSCT) is a treatment for many serious haematological malignancies. Despite advances in pre- and post-transplant management, a significant proportion of patients still develop adverse effects such as graft-versus-host disease (GvHD), relapse or cytomegalovirus reactivation. These reactions can significantly reduce patients' quality of life and may even be fatal. Invariant NKT cells (hereafter referred to as iNKT cells) are a rare population of T lymphocytes that play an important role in regulating the immune response. Depending on the expression of CD4 and CD8 markers, they can be divided into several subpopulations. iNKT cells can simultaneously support both Th1 and Th2 immune responses while suppressing the inflammatory response. Therefore, they appear to be suitable for treating diseases involving deregulated immunity, such as GvHD, autoimmune diseases, and oncological diseases. The concentration of iNKT cells after HSCT is highly variable. According to the available data, iNKT cell kinetics correspond to the severity of GvHD, as well as the risk of relapse and the development of infectious complications. However, these data are usually obtained using locally set protocols and come from single-centre measurements, which reduces their validity and clinical utility as both a biomarker and background data for possible allogeneic applications of iNKT cells in patients with low levels. To eliminate bias caused by specific local data processing and provide a robust dataset, a multicentre study is necessary to yield a representative set of results, as this is the only way to definitively establish the impact of iNKT cell levels on post-transplant outcomes. Flow cytometric analysis enables the combined examination of specific markers on the surface of cells and inside them. Due to the increasing complexity and heterogeneity of protocols, antibody manufacturers often resort to standardised dried panels, which ensure high consistency of measured data.
This project will involve monitoring iNKT cells at defined time points following allogeneic transplantation. The project's outcomes will be to determine the feasibility of standardising iNKT monitoring using the DryTube flow cytometry assay, establish differences in iNKT levels in transplanted patients across different centres, and estimate the association between iNKT levels and post-transplant complications.
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Monika Holubová, MSc.
- 電話番号:+420 377 103 991
- メール:holubovam@fnplzen.cz
研究連絡先のバックアップ
- 名前:Lenka Lukášová, MD, MSc.
- 電話番号:+420 377 103 871
- メール:LUKASOVALE@fnplzen.cz
研究場所
-
-
Czechia
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Pilsen、Czechia、チェコ、32300
- 募集
- University Hospital Pilsen
-
コンタクト:
- Monika Holubová, MSc.
- 電話番号:+420 377 103 991
- メール:holubovam@fnplzen.cz
-
コンタクト:
- Lenka Lukášová, MD, MSc.
- 電話番号:+420 377 103 871
- メール:LUKASOVALE@fnplzen.cz
-
主任研究者:
- Michal Karas, MD, MSc.
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Diagnosis: AML (exlusion of secondary disease)
- Disease status at time of HSCT: complete remission
- Karnofsky performance status: ≥80%
- Source of HSC: PBSC
Exclusion Criteria:
- Prior transplant
- Uncontrolled Malignancy
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
HSCT patients
Patients who have undergone allogeneic hematopoietic cell transplantation and have been diagnosed with acute myeloid leukemia.
|
Blood draw for diagnostic test
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Detection of peripheral blood iNKTs after HSCT using flow cytometry
時間枠:Day 30, day 60, day 90
|
iNKTs will be monitored in peripheral blood using a mixture of dried antibodies and bulk lysis and flow cytometry.
This mixture of antibodies contains the specific iNKT marker (TCRVα24Jα18) and markers for the main subsets.
The percentage of iNKT cells among leukocytes and T cells, as well as the proportion of CD4 and CD8 iNKT subsets, will be provided.
|
Day 30, day 60, day 90
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Absolute Number of Circulating iNKT Cells and Their Dynamics After HSCT
時間枠:Day 30, day 60, day 90
|
Leukocyte count will be estimated through hematological analysis, and circulating iNKTs will be counted based on flow cytometry percentage in Patient´s Peripheral Blood At day + 30, +60, +90 After HSCT.
The level of iNKTs will be reported as the number of cells per milliliter of peripheral blood.
|
Day 30, day 60, day 90
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Correlation of iNKT cell levels with Post-transplant Complications
時間枠:Day 30, day 60, day 90
|
Correlation of iNKT cell levels with Post-transplant Complications
|
Day 30, day 60, day 90
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- QiNKT-HSCT
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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