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Evaluation of mRNA Expression of CD244 and Its Adapter Molecules in CD8+ T Cells in Acute Leukemia.
Mohammadi, Maryam; Asgarian-Omran, Hossein; Najafi, Ahmad; Valadan, Reza; Karami, Hossein; Naderisoraki, Mohammad; Zaboli, Ehsan; Eslami, Mohammad; Tehrani, Mohsen.
Affiliation
  • Mohammadi M; Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
  • Asgarian-Omran H; Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
  • Najafi A; Gastrointestinal Cancer Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
  • Valadan R; Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
  • Karami H; Molecular and Cell-Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
  • Naderisoraki M; Thalassemia Research Center (TRC), Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Mazandaran Iran.
  • Zaboli E; Thalassemia Research Center (TRC), Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Mazandaran Iran.
  • Eslami M; Gastrointestinal Cancer Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
  • Tehrani M; Department of Hematology and Oncology, Imam Khomeini hospital, Mazandaran university of Medical Sciences, Sari, Iran.
Iran Biomed J ; 27(4): 214-8, 2023 07 01.
Article in En | MEDLINE | ID: mdl-37634081
ABSTRACT

Background:

This study investigated the role of the immune-checkpoint receptor (ICR), CD244, and its adapter molecules, in CD8+ T cells in acute leukemia.

Methods:

Blood samples were obtained from 21 acute lymphoblastic leukemia (ALL) and 6 acute myeloid leukemia (AML) patients and 20 control subjects. Relative gene expression of CD244, immune receptor tyrosine-based switch motif-associated protein (SA), EWS/FLI1-activated transcript 2 (EAT-2), and LncRNA-GSTT1-AS1 were evaluated using quantitative reverse transcription polymerase chain reaction.

Results:

Expression of CD244, SAP, and EAT-2 were significantly lower in CD8+ T cells from ALL patients than those from control subjects. Interestingly, the expression of SAP was much lower than that of CD244, indicating a lower ratio of SAP to CD244. Also, SAP expression was significantly lower in AML patients compared to the control group. Expression of LncRNA-GSTT1-AS1 showed no significant difference in ALL and AML patients compared to control subjects.

Conclusion:

The low SAP/CD244 expression ratio in CD8+ T cells in ALL suggests an inhibitory role for CD244 in ALL.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / RNA, Long Noncoding Limits: Humans Language: En Journal: Iran Biomed J Journal subject: BIOLOGIA / MEDICINA Year: 2023 Document type: Article Affiliation country: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / RNA, Long Noncoding Limits: Humans Language: En Journal: Iran Biomed J Journal subject: BIOLOGIA / MEDICINA Year: 2023 Document type: Article Affiliation country: Iran