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1.
Vopr Virusol ; 61(2): 69-73, 2016.
Artigo em Russo | MEDLINE | ID: mdl-27451498

RESUMO

Studies of the primary cultures of granulocytes, mononuclear, and monocyte-macrophage cells derived from human blood were performed using variola virus (VARV) in the doses of 0.001-0.021 PFU/cell (plaques-forming units per cell). Positive dynamics of the virus accumulation was observed only in the monocyte-macrophages with maximum values of virus concentration (5.0-5.5 Ig PFU/ml) mainly within six days after the infection. The fact of VARV replication in the monocyte-macrophages was confirmed by the data of electron microscopy. At the same time, virus vaccines when tested in doses 3.3 and 4.2 Ig PFU/ml did not show the ability to reproduce in these human cells. The people sensitivity to VARV as assessed from the data obtained on human monocyte-macrophages corresponded to -1 PFU (taking into account the smooth interaction of the virus in the body to the cells of this type), which is consistent to previously found theoretical data on the virus sensitivity. The human susceptibility to VARV assessed experimentally can be used to predict the adequacy of developed smallpox models (in vivo) based on susceptible animals. This is necessary for reliable assessment of the efficiency of development of drugs for treatment and prophylaxis of the smallpox.


Assuntos
Macrófagos/virologia , Varíola/prevenção & controle , Vírus da Varíola/fisiologia , Vírion/crescimento & desenvolvimento , Adulto , Animais , Anticorpos Antivirais/sangue , Granulócitos/imunologia , Humanos , Macrófagos/ultraestrutura , Masculino , Microscopia Eletrônica , Especificidade de Órgãos , Cultura Primária de Células , Varíola/sangue , Varíola/imunologia , Varíola/virologia , Vacina Antivariólica/farmacologia , Vírus da Varíola/ultraestrutura , Vírion/ultraestrutura , Replicação Viral
2.
Vopr Virusol ; 53(1): 27-31, 2008.
Artigo em Russo | MEDLINE | ID: mdl-18318132

RESUMO

A genetic construct of the human interleukin-2 (IL-2) gene within vaccinia virus (L-IVP strain) has been designed. The authors show the capacity of CV-1 cells infected with the recombinant vaccinia virus VV-SIL2 to secrete human IL-2 into the culture medium. Human IL-2 has been detected by immunoblotting. The sera from the animals immunized with the recombinant virus VV-SIL2 exhibited both human IL-2 and its antibodies throughout the observation period. This recombinant virus immunization induced both humoral and cell-mediated immune responses to human IL-2; the observed changes in the concentrations of cytokines are likely to suggest that the response predominantly followed a Th1 pathway. The study construct was nontoxic at the used concentrations and administration routes. The findings point that it is promising to investigate the adjuvant properties of the recombinant VV-SIL2 vaccine-based preparation for immunization in combination with various vaccines and to study this construct in therapy for cancer diseases.


Assuntos
Anticorpos Antivirais/sangue , Imunização , Interleucina-2/genética , Interleucina-2/imunologia , Infecções por Poxviridae/sangue , Infecções por Poxviridae/imunologia , Vacina Antivariólica/imunologia , Vaccinia virus/genética , Vaccinia virus/imunologia , Animais , Linhagem Celular , Citocinas/sangue , Humanos , Técnicas Imunoenzimáticas , Injeções Subcutâneas , Interleucina-2/sangue , Ativação Linfocitária , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Vacina Antivariólica/administração & dosagem , Vacina Antivariólica/genética , Baço/imunologia , Células Th1/imunologia , Vacinas Sintéticas/administração & dosagem , Vacinas Sintéticas/imunologia
3.
Probl Tuberk Bolezn Legk ; (2): 38-42, 2007.
Artigo em Russo | MEDLINE | ID: mdl-17419334

RESUMO

The protective properties of artificial mycobacterial particles versus BCG vaccine were studied in laboratory animals with experimental tuberculosis. The findings of the decreased rate of a tuberculous process and on the increased mean life span in animals inoculated with M. bovis suggest that immunization of guinea-pigs with mycobacterial particles promotes the enhanced development of antituberculous immunity in the animals. The paper proposes a promising method for designing artificial immunogens, the high-polymer antigenic structures that imitates mycobacterial particles.


Assuntos
Vacina BCG/imunologia , Mycobacterium bovis/imunologia , Vacinas contra a Tuberculose/imunologia , Tuberculose/prevenção & controle , Vacinas Sintéticas/imunologia , Animais , Interpretação Estatística de Dados , Modelos Animais de Doenças , Cobaias , Imunização , Técnicas Imunoenzimáticas , Fagocitose , Tuberculose/imunologia
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