Vol 57, No 2 (2012)

The review analyzes recent data and current ideas on the enzyme cyclooxygenase 2 (COX-2) as a possible biomarker of virus-associated human malignant neoplasm. Possible mechanisms of COX-2 activation in the cells infected with oncogenic human viruses, such as hepatitis B virus, Epstein-Barr virus, and human papillomavirus are considered in detail.

The paper provides a theoretical analysis for determining whether the antiviral nonspecific drugs being tested are promising to solve biosafety problems in the treatment of exotic viral infections. The essence of the proposed concept of evaluation of protective effectiveness is to analyze the effect of a test drug on the pathogenesis of experimental infection from the fact that it is effective in adequately eliminating the animal-simulated leading syndrome of human disease. The given approaches to using adequacy criteria to select the species of animals meeting the goals of tests in terms of pathogenetic and pharmacological parameters determine a new methodology for evaluating the efficacy of protective agents. Basic requirements for a testing procedure are presented. The prognostic value of evaluation of the protective efficacy of antiviral agents for man will depend on the approximation of the pathogenetic features and external manifestation of disease in the selected animal species to human infection. The paper also covers the comparative characteristics of the course of Ebola fever and Venezuelan equine encephalomyelitis in man and some species of monkey.

The self-assembly of marine macrophyte glycolipids, holothurian saponin, and cholesterol gave rise to nanoscale morphological structures called tubular immunostimulating (TI) complexes. Whether the latter could be used on the basis of vaccine preparations containing the influenza virus subunit antigens was studied. there was an obvious increase in the immunogenicity of influenza virus hemagglutinin when the experimental animals were immunized with this antigen as part of TI complexes. It was shown that the adjuvant activity of the TI complex to influenza virus hemagglutinin could be enhanced by adding the known antioxidant echinochrome a from a sand-dollar (echinarachnius parma) to the matrix of the TI complex.

The use of the RNA interference technique yielded data on the antiviral activity of small interfering RNA (siRNA) oligonucleotides against hepatitis С virus (HCV) infection in the pig embryo kidney (SPEV) cell cultures. The RNA interference technique is based on the specific recognition of the mRNA target by using the specially designed siRNA (19-22 bp) oligonucleotides. in particular, it was shown that siRNA added to the monolayer of HCv-infected sPEv cells resulted in the protection of the infected cells against the cytopathogenic activity of the virus. The results were confirmed in the experiments that demonstrated the ability of RNA oligonucleotides to reduce the production of infectious (cytopathogenic) HCV by infected SPEV cells in early-stage infection.

The currently used tick-borne encephalitis virus vaccines are based on the inactivation of tick-borne encephalitis virus (TBEV) of Far Eastern or West European genetic types from the primary cultures of chick embryo fibroblasts. Since the WHO recommends that vaccines should be designed using continuous cell cultures rather than chick embryos as a substrate, this investigation has compared the infection of continuous monolayer SPEV, Vero E6, and vaccine line Vero (B) cell cultures with TBEV strains of the Siberian and Far Eastern genetic types dominating in the endemic regions of Russia. After cell infection with Far Eastern (Sofyin and 205 strains) or Siberian (Aina, 2530, 2689, and 2703 strains) TBEV genetic types, the viable TBEV titers reached 2.8 lg CPD50 for Vero (B) cells, 5.5 lg CPD50 for Vero E6 cells, and up to 9 lg CPD50 for SPEV cells. The quantitative scores of TBEV E antigen in enzyme immunoassay (EiA) and genome equivalents by reverse-transcription polymerase chain reaction (PCR), followed by real-time PCR, permitted one to estimate as high as 108 virions in 1 ml of culture fluid, which corresponded to those of the microscopic observations of CPD for SPEV cells and substantially exceeded the values for Vero E6 cells, and for Vero (B) cells in particular. The data of TBEV strain titration, EiA, and realtime reverse-transcription PCR suggest that the Russian vaccine Vero (B) cell line defined as meeting the WHO requirements, as well as Vero E6 cells may be used to design tick-borne encephalitis vaccine.