Inflammatory Cytokine-Producing Cells and Inflammation Markers in the Synovium of Osteoarthritis Patients Evidenced in Human Herpesvirus 7 Infection

Autor: Mihails Tarasovs, Sofija Semenistaja, Zaiga Nora-Krukle, Modra Murovska, Valerija Groma, Sandra Skuja, Simons Svirskis
Rok vydání: 2020
Předmět:
0301 basic medicine
Male
medicine.medical_treatment
viruses
Herpesvirus 7
Human

lcsh:Chemistry
0302 clinical medicine
Virus latency
Medicine
lcsh:QH301-705.5
Spectroscopy
Aged
80 and over

Synovitis
Synovial Membrane
virus diseases
General Medicine
Middle Aged
Computer Science Applications
Cytokine
medicine.anatomical_structure
PCR
immunohistochemistry
CD4 Antigens
Cytokines
Tumor necrosis factor alpha
ELISA
Female
medicine.symptom
Adult
Roseolovirus Infections
Inflammation
synovium
Article
Catalysis
Inorganic Chemistry
03 medical and health sciences
HHV-7
Immune system
Antigen
Osteoarthritis
Humans
Physical and Theoretical Chemistry
Molecular Biology
Aged
030203 arthritis & rheumatology
business.industry
Interleukin-6
Tumor Necrosis Factor-alpha
Organic Chemistry
medicine.disease
cytokines
osteoarthritis
030104 developmental biology
lcsh:Biology (General)
lcsh:QD1-999
Immunology
DNA
Viral

Synovial membrane
business
Biomarkers
Zdroj: International Journal of Molecular Sciences
Volume 21
Issue 17
International Journal of Molecular Sciences, Vol 21, Iss 6004, p 6004 (2020)
ISSN: 1422-0067
Popis: A direct association between joint inflammation and the progression of osteoarthritis (OA) has been proposed, and synovitis is considered a powerful driver of the disease. Among infections implicated in the development of joint disease, human herpesvirus 7 (HHV-7) infection remains poorly characterized. Therefore, we assessed synovitis in OA patients
determined the occurrence and distribution of the HHV-7 antigen within the synovial membrane of OA-affected subjects
and correlated plasma levels of the pro-inflammatory cytokines tumor necrosis factor (TNF), interleukin-6 (IL-6), and TNF expressed locally within lesioned synovial tissues with HHV-7 observations, suggesting differences in persistent latent and active infection. Synovial HHV-7, CD4, CD68, and TNF antigens were detected immunohistochemically. The plasma levels of TNF and IL-6 were measured by an enzyme-linked immunosorbent assay. Our findings confirm the presence of persistent HHV-7 infection in 81.5% and reactivation in 20.5% of patients. In 35.2% of patients, virus-specific DNA was extracted from synovial membrane tissue samples. We evidenced the absence of histopathologically detectable synovitis and low-grade changes in the majority of OA patients enrolled in the study, in both HHV-7 PCR+ and HHV-7 PCR‒ groups. The number of synovial CD4-positive cells in the HHV-7 polymerase chain reaction (PCR)+ group was significantly higher than that in the HHV-7 PCR‒ group. CD4- and CD68-positive cells were differently distributed in both HHV-7 PCR+ and HHV-7 PCR‒ groups, as well as in latent and active HHV-7 infection. The number of TNF+ and HHV-7+ lymphocytes, as well as HHV-7+ vascular endothelial cells, was strongly correlated. Vascular endothelial cells, especially in the case of infection reactivation, appeared vulnerable. The balance between virus latency and reactivation is a long-term relationship between the host and infectious agent, and the immune system appears to be involved in displaying overreaction when a shift in the established equilibrium develops.
Databáze: OpenAIRE