Projects per year
Abstract
BACKGROUND AND AIM:Infections and immune deregulation frequently complicate chronic lymphocytic leukemia (CLL) disease. In immunocopromised individuals, EBV can either become reactivated or establish latency programs II and III. The aim of this study was to analyze the types of EBV infection in newly-diagnosed CLL patients with the CD38-negative (CD38<6%), CD38-moderate (CD38>6%<30%), and CD38-positive (CD38>30%) leukemic cells in peripheral blood (PB).
METHODS:PB cells of 53 newly diagnosed CLL patients were examined for the EBV copy number and mRNA expression of the EBV-encoded genes, BZLF, LMP1, EBNA2, and LMP2A, and the CLL negative prognostic ZAP70. RESULTS:There were not significant differences in the ZAP70 mRNA levels between the CLL patient groups. In the CD38-negative patients (n=21), the EBV copy number was low (< 29 copies per 105 cells) or undetectable. In two patients of the CD38-moderate group (n=20), the EBV copy number was 264 and 522. In the CD38-positive group (n=12), in one patient, 250 EBV copies were detected. BZLF mRNA was found in one patient of the CD38-positive group, indicating early stage of lytic EBV infection. LMP1 mRNA was detected in two patients in the CD38-positive group: one patient had EBNA2 mRNA, another one was EBNA2-negative but LMP2A-positive what suggest the latency type II and III, respectively.
CONCLUSIONS:Possible EBV involvement was revealed in 5 out of 53 patients with newly diagnosed CLL. To assess the putative role of EBV in CLL progression, following up of these patients is being conducted. The studies were funded by the Latvian Council of Science projects No.651/2014 and No.lzp-2018/1-0156.
METHODS:PB cells of 53 newly diagnosed CLL patients were examined for the EBV copy number and mRNA expression of the EBV-encoded genes, BZLF, LMP1, EBNA2, and LMP2A, and the CLL negative prognostic ZAP70. RESULTS:There were not significant differences in the ZAP70 mRNA levels between the CLL patient groups. In the CD38-negative patients (n=21), the EBV copy number was low (< 29 copies per 105 cells) or undetectable. In two patients of the CD38-moderate group (n=20), the EBV copy number was 264 and 522. In the CD38-positive group (n=12), in one patient, 250 EBV copies were detected. BZLF mRNA was found in one patient of the CD38-positive group, indicating early stage of lytic EBV infection. LMP1 mRNA was detected in two patients in the CD38-positive group: one patient had EBNA2 mRNA, another one was EBNA2-negative but LMP2A-positive what suggest the latency type II and III, respectively.
CONCLUSIONS:Possible EBV involvement was revealed in 5 out of 53 patients with newly diagnosed CLL. To assess the putative role of EBV in CLL progression, following up of these patients is being conducted. The studies were funded by the Latvian Council of Science projects No.651/2014 and No.lzp-2018/1-0156.
Original language | English |
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Pages | 218 |
Number of pages | 1 |
Publication status | Published - 15 Sept 2021 |
Event | 23rd Annual Conference of the European Society for Clinical Virology - Manchester, United Kingdom Duration: 15 Sept 2021 → 18 Sept 2021 Conference number: 23 https://www.escv2021.org/conference-information/about-escv/ https://healthmanagement.org/c/hospital/event/23rd-annual-conference-of-the-european-society-for-clinical-virology |
Conference
Conference | 23rd Annual Conference of the European Society for Clinical Virology |
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Abbreviated title | ESCV 2021 |
Country/Territory | United Kingdom |
City | Manchester |
Period | 15/09/21 → 18/09/21 |
Internet address |
Field of Science*
- 1.6 Biological sciences
- 3.3 Health sciences
Publication Type*
- 3.4. Other publications in conference proceedings (including local)
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Dive into the research topics of 'EPSTEIN BARR VIRUS INFECTION IN NEWLY DIAGNOSED CD38-POSITIVE AND CD38-NEGATIVE PATIENTS WITH CHRONIC LYMPHOCYTIC LEUKEMIA'. Together they form a unique fingerprint.Projects
- 1 Finished
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Investigation of the chemokine receptors CCR1 and CCR2 and EBV infection aimed on disclosure of new markers that can predict the high risk for progression of chronic lymphocytic leukemia
Holodņuka, I. (Project leader), Kozireva, S. (Participant), Zvejniece, L. (Expert (PhD student)), Pavlova, J. (Participant) & Demida, O. (Assistant (student))
31/08/18 → 30/11/21
Project: Fundamental and Applied Research Programme