Back to Search Start Over

Change in Programmed Death-1 And Inducible Costimulator Expression in Patients with Acute Myeloid Leukemia Following Chemotherapy and Its Cytogenetic Abnormalities

Authors :
Mahdiyar Iravani Saadi
Maryam Ahmadyan
Heeva Jalali
Nasrin Noshadi
Mitra Moradi
Fatemeh Mardani Valandani
Nadiya Kheradmand
Hossain Ali Rostamipour
Fakhroddin Hosseini
Amir Ali Hamidieh
Abolfazl Khalafi-Nezhad
Source :
Galen Medical Journal. 11:e2394
Publication Year :
2022
Publisher :
Salvia Medical Sciences Ltd, 2022.

Abstract

Background: Programmed death-1 (PD-1) and inducible costimulator (ICOS) are immune checkpoint receptors participating in tumor immune evasion, which counters the activation signal provided through the T-cell receptor ligation. This study aimed to investigate the relationship between the expression of PD-1 and ICOS on mononuclear cells (MNCs) isolated from the peripheral blood of acute myeloid leukemia (AML) patients and their response to induction chemotherapy. Materials and Methods: Peripheral blood samples (5cc) were collected from 56 AML patients at first diagnosis before and after the induction therapy regimen for AML. PD-1 and ICOS expression were analyzed in all patients before and after the standard induction therapy regimen. Results: The expression of PD-1 and ICOS significantly decreased (66.7 and 16.3 fold, respectively) in AML patients following chemotherapy compared to its baseline value (P=0.01 and P=0.001, respectively). The expressions of PD-1 and ICOS were significantly different between favorable and poor risk groups. Conclusions: Lower PD-1 and ICOS expressions on the surface of MNCs before induction therapy were associated with a better response to treatments. In addition, PD-1 and ICOS expression on MNCs decreased after induction therapy.

Subjects

Subjects :
General Medicine

Details

ISSN :
23222379 and 25882767
Volume :
11
Database :
OpenAIRE
Journal :
Galen Medical Journal
Accession number :
edsair.doi...........c43fcb62d569ba54eda803b8bcdccf50
Full Text :
https://doi.org/10.31661/gmj.v11i.2394