Markers of Epstein–Barr virus in clinical assessment of Russian patients with nasopharyngeal cancer
- Authors: Smirnova K.V.1,2, Senuta N.B.1, Botezatu I.V.1, Ignatova A.V.3,4, Dushenkina T.E.1, Zolotarev A.A.3, Lichtenstein A.V.1, Gurtsevich V.E.1
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Affiliations:
- Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation
- N.I. Pirogov Russian National Research Medical University
- Russian Medical Academy of Continuing Professional Education, Ministry of Health of Russia
- Peoples’ Friendship University of Russia
- Issue: Vol 8, No 3 (2021)
- Pages: 14-24
- Section: RESEARCH ARTICLES
- Published: 05.11.2021
- URL: https://umo.abvpress.ru/jour/article/view/376
- DOI: https://doi.org/10.17650/2313-805X-2021-8-3-14-24
- ID: 376
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Full Text
Abstract
Introduction. Epstein–Barr virus (EBV) is equally widespread in the endemic and non-endemic world regions for nasopharyngeal cancer (NPC). High incidence of NPC in endemic countries and low in non-endemic countries suggest there are different mechanisms and conditions for tumor occurrence and, possibly, different clinical significance of EBV-associated markers. However, significance of these markers for determining NPC in non-endemic regions is still poorly understood. Objective – to determine clinical significance of titers of IgG/IgA antibodies to EBV capsid antigen and concentrations of the viral DNA in patients’ blood plasma as diagnostic and monitoring markers for NPC in a non-endemic region of Russia. Materials and methods. Titers of EB-specific antibodies were determined by indirect immunofluorescence, and concentration of the viral DNA in plasma was measured using a quantitative polymerase chain reaction in real time. Study group included patients with NPC (n = 96), and control group – blood donors (n = 171) and patients with other head and neck tumors (n = 33).
Results. Titers of IgG/IgA antibodies to EBV capsid antigen, being an important diagnostic marker of nasopharyngeal cancer, did not always correlate with patients’ clinical condition. Humoral response to emerging events often delayed due to inertia of the immune system. Concentration of EBV DNA in patients’ blood plasma clearly reflected the dynamics of the pathological process: it decreased to background values in remission and increased while the disease progressed. In contrast to endemic regions, we did not find any correlation between the studied EBV markers and clinical manifestations of the disease, evaluated in accordance with the TNM classification (Tumor, Nodus and Metastasis).
Conclusion. In non-endemic countries, such as Russia, serological and molecular markers of EBV can be successfully used for the primary diagnosis of NPC. However, for the disease monitoring, it is preferable to use the value of the concentrations of circulating EBV DNA, which, in contrast to the values of IgG/IgA antibody titers to VCA EBV, more accurately reflect the patient’s clinical condition.
About the authors
K. V. Smirnova
Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation; N.I. Pirogov Russian National Research Medical University
Author for correspondence.
Email: fake@neicon.ru
ORCID iD: 0000-0001-6209-977X
24 Kashirskoe Shosse, Moscow 115478
1 Ostrovityanova St., Moscow 117997
Russian FederationN. B. Senuta
Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation
Email: fake@neicon.ru
ORCID iD: 0000-0001-8915-8274
24 Kashirskoe Shosse, Moscow 115478
Russian FederationI. V. Botezatu
Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation
Email: fake@neicon.ru
ORCID iD: 0000-0002-0297-4963
24 Kashirskoe Shosse, Moscow 115478
Russian FederationA. V. Ignatova
Russian Medical Academy of Continuing Professional Education, Ministry of Health of Russia; Peoples’ Friendship University of Russia
Email: fake@neicon.ru
Bld. 1, 1/2 Barrikadnaya St., Moscow 125993
6 Miklukho-Maklaya St., Moscow 117198
Russian FederationT. E. Dushenkina
Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation
Email: fake@neicon.ru
ORCID iD: 0000-0001-8279-514X
24 Kashirskoe Shosse, Moscow 115478
Russian FederationA. A. Zolotarev
Russian Medical Academy of Continuing Professional Education, Ministry of Health of Russia
Email: fake@neicon.ru
Bld. 1, 1/2 Barrikadnaya St., Moscow 125993
Russian FederationA. V. Lichtenstein
Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation
Email: fake@neicon.ru
ORCID iD: 0000-0002-0190-5069
24 Kashirskoe Shosse, Moscow 115478
Russian FederationV. E. Gurtsevich
Research Institute of Carcinogenesis N.N. Blokhin National Medical Research Center of Oncology оf the Ministry of Health of the Russian Federation
Email: fake@neicon.ru
ORCID iD: 0000-0003-1840-4364
24 Kashirskoe Shosse, Moscow 115478
Russian FederationReferences
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