Evaluation of Immune Status Before and After Splenectomy in Immune Thrombocytopenia Patients

Sponsor
Zhang Lei (Other)
Overall Status
Recruiting
CT.gov ID
NCT03998059
Collaborator
(none)
50
1
42
1.2

Study Details

Study Description

Brief Summary

Evaluation of immune status before and after splenectomy in immune thrombocytopenia patients.

Condition or Disease Intervention/Treatment Phase
  • Procedure: splenectomy

Detailed Description

A total of 30 ITP patients will be enrolled in the study. These patients should fail to have sustained response to multiple first- and second-line treatments of ITP and agree to have splenectomy. Before splenectomy, these patients will be reassessed and still diagnosed with ITP.Their platelet level will be raised to a safe state before surgery, and the laparoscopic splenectomy will be performed in Tianjin People's Hospital. The investigators plan to take 20ml of peripheral blood (PB) of these patients at 6 time points, including 1 day before surgery, 1 week, 1 month, 3 months, 6 months, and 12 months after surgery, and take a small amount of spleen tissue during surgery.

18 age- and gender- matched healthy donor will also be enrolled as controls and taken 20ml of peripheral blood. The investigators also plan to take splenic tissue from 10 patients who have splenectomy due to Hereditary spherocytosis or trauma.

And then the investigators will do the experiments step by step. 1, Isolation of peripheral blood and splenic mononuclear cells;2, Detection of the percentage of cell population;3, Activation and proliferation of B lymphocyte; 4, Activation and proliferation of T lymphocyte;5,Apoptosis of platelets by cytotoxic T cells;6,Phagocytosis of platelets by macrophages in spleen;7,Enzyme-linked immunosorbent assay (ELISA) for cytokines.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Evaluation of Immune Status Before and After Splenectomy in Immune Thrombocytopenia Patients
Actual Study Start Date :
Jan 23, 2019
Anticipated Primary Completion Date :
Jan 23, 2022
Anticipated Study Completion Date :
Jul 23, 2022

Arms and Interventions

Arm Intervention/Treatment
30 immune thrombocytopenia(ITP) patients

A total of 30 cases. The investigators plan to take 20ml of peripheral blood (PB) of these 30 ITP patients at 6 time points, including 1 day before surgery, 1 week, 1 month, 3 months, 6 months, and 12 months after surgery

Procedure: splenectomy
These patients should fail to have sustained response to multiple first- and second-line treatments of ITP and agree to have splenectomy.Before splenectomy, these patients will be reassessed and still diagnosed with ITP.Their platelet level will be raised to a safe state before surgery, and the laparoscopic splenectomy will be performed in Tianjin People's Hospital.

20 normal controls

A total of 20 cases.18 age- and gender- matched healthy donor will also be enrolled as controls and taken 20ml of peripheral blood.

Spleens of the 30 cases patients(ITP)

These 30 ITP patients agree to have splenectomy.The investigators will take a small amount of spleen tissue during surgery.

Spleens of the 10 cases patients(normal controls)

The investigators also plan to take splenic tissue from 10 patients who have splenectomy due to hereditary spherocytosis or trauma.

Outcome Measures

Primary Outcome Measures

  1. Changes of the percentage of cell population [1 year]

    To assess the changes of the percentage of B cell subsets,regulatory B cells(Breg),regulatory T cells (Treg),supressor T cells(Ts),monocyte Fc receptor(FCR)I/II, FCRIII and FCRIIb, helper T cells(Th)subsets and the functionally-polarized CD4+ T cell subsets in peripheral blood mononuclear cells(PBMCs)at 6 time points, including 1 day before surgery, 1 week, 1 month, 3 months, 6 months, and 12 months after surgery, and to compare with the healthy controls.

  2. Changes of activation and proliferation of B and T lymphocyte, apoptosis of platelets by cytotoxic T cells(CTLs) [1 year]

    To assess the changes of activation and proliferation of B and T lymphocyte, apoptosis of platelets by cytotoxic T cells(CTLs) in peripheral blood mononuclear cells(PBMCs)at 6 time points, including 1 day before surgery, 1 week, 1 month, 3 months, 6 months, and 12 months after surgery, and to compare with the healthy controls.

  3. Changes of cytokines in the cell culture supernatants and plasma [1 year]

    To assess the changes of cytokines in the cell culture supernatants and plasma at 6 time points, including 1 day before surgery, 1 week, 1 month, 3 months, 6 months, and 12 months after surgery, and to compare with the healthy controls.

Secondary Outcome Measures

  1. Changes of phagocytosis of platelets by macrophages in itp patients spleen and the normal spleen controls. [The day of the splenectomy]

    To assess the changes of phagocytosis of platelets by macrophages in itp patients spleen and the normal spleen controls.

  2. Changes of the percentage of cell population, activation and proliferation of B and T lymphocyte, apoptosis of platelets by cytotoxic T cells(CTLs) in itp patients spleen and the normal spleen controls. [The day of the splenectomy]

    To assess the changes of the percentage of B cell subsets,regulatory B cells(Breg),regulatory T cells (Treg),supressor T cells(Ts),monocyte Fc receptor(FCR)I/II, FCRIII and FCRIIb, helper T cells(Th)subsets ,the functionally-polarized CD4+ T cell subsets, activation and proliferation of B and T lymphocyte, apoptosis of platelets by cytotoxic T cells(CTLs) in itp patients spleen and the normal spleen controls.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged 18 to 60 years old, male or female;

  • Conform to the diagnostic criteria of immune Thrombocytopenia (ITP)

  • Needed splenectomy;

  • People who are willing to sign the informed consent voluntarily and follow the research program.

Exclusion Criteria:
  • Secondary thrombocytopenic purpura;

  • Patients with poor compliance;

  • Researchers believe that patients should not participate in the test of any other condition.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yunfei Chen Tianjin Tianjin China 300020

Sponsors and Collaborators

  • Zhang Lei

Investigators

  • Principal Investigator: Lei Zhang, MD, Chinese Academy of Medical Science and Blood Disease Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Zhang Lei, vice Director of Thrombosis and Hemostasis Center, Institute of Hematology & Blood Diseases Hospital
ClinicalTrials.gov Identifier:
NCT03998059
Other Study ID Numbers:
  • KT2018087-EC-1
First Posted:
Jun 25, 2019
Last Update Posted:
Aug 27, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Zhang Lei, vice Director of Thrombosis and Hemostasis Center, Institute of Hematology & Blood Diseases Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 27, 2021