Clinical Trial Details
— Status: Recruiting
Administrative data
NCT number |
NCT04657237 |
Other study ID # |
359 |
Secondary ID |
|
Status |
Recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
January 2017 |
Est. completion date |
November 2021 |
Study information
Verified date |
December 2020 |
Source |
Assiut University |
Contact |
shereen M kamal, assocate professor |
Phone |
01006279209 |
Email |
sheridouh79[@]yahoo.com |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Surgery is first-line treatment for solid tumors. However, surgical trauma-induced
physiologic stress has been demonstrated to facilitate metastasis and recurrence in different
types of cancer. It has been reported that the PD-1/PD-L1 pathway could be activated by
surgical stress. Hence, we instigate the effect of anesthetic technique on expression of PD1
and PD1 ligand.
Description:
The cellular immune response plays a central part in postoperative clearance of tumor cells.
T lymphocytes and natural killer (NK) cells are two predominant cytotoxic effector cells that
are the major components of antitumor immunity. In mouse models, proliferation of T
lymphocytes in response to surgical trauma is defective . Programmed death-1 (PD-1) belongs
to the CD28 receptor superfamily. It is an inhibitory receptor, and its expression is
upregulated on activated leukocytes, resulting in an inhibited immune response. PD-1
interacts with two ligands: programmed death ligand-1 (PD-L1, also referred to as B7-H1) and
programmed death ligand-2 (PD-L2, also known as B7-DC). PD-L2 is expressed mainly on
activated dendritic cells (DCs) and macrophages, whereas PD-L1 is distributed widely. In
addition to immune cells, some subsets of tumor cells also express PD-L1 to escape from
immunosurveillance. It has been reported that the PD-1/PD-L1 pathway could be activated by
surgical stress. Hence, we instigate the effect of anesthetic technique on expression of PD1
and PD1 ligand.