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1.
Adv Gerontol ; 22(4): 676-9, 2009.
Artigo em Russo | MEDLINE | ID: mdl-20405739

RESUMO

There are an increased spontaneous platelet aggregation and decreased ADP-induced platelet aggregation in old-aged people with diabetes I than in healthy subjects. In diabetes II the ADP-induced platelet aggregation was increased. In diabetes I and II intravascular coagulation strengthens, while in II type diabetes these changes are less, than in type I. It is associated with a later age of diabetes II and its complications occurrence.


Assuntos
Envelhecimento/sangue , Diabetes Mellitus Tipo 1/sangue , Diabetes Mellitus Tipo 2/sangue , Hemostasia/fisiologia , Interpretação Estatística de Dados , Diabetes Mellitus Tipo 1/tratamento farmacológico , Diabetes Mellitus Tipo 1/epidemiologia , Diabetes Mellitus Tipo 2/tratamento farmacológico , Diabetes Mellitus Tipo 2/epidemiologia , Feminino , Humanos , Insulina/administração & dosagem , Insulina/uso terapêutico , Masculino , Pessoa de Meia-Idade , Agregação Plaquetária/fisiologia
2.
Bioorg Khim ; 34(5): 639-44, 2008.
Artigo em Russo | MEDLINE | ID: mdl-19060938

RESUMO

We and other authors have recently shown that the pattern of the immune response to components of anthrax, the Bacillus anthracis lethal toxin, is complex. In addition to neutralizing antibodies, the antitoxin antibody pool contains antibodies enhancing the toxin lethal action. We mapped the epitopes in the protective antigen that are responsible for the induction of both antibody types. In this study, we obtained new data on the cytotoxicity of the B. anthracis lethal toxin toward the J774 A.1 cell line in the presence of monoclonal antibodies to various domains of the protective antigen and the lethal factor. The role of the Fc fragment of immunoglobulins in enhancing the lethal toxin action was shown. These results may serve as a basis for the development of a new generation vaccine for anthrax.


Assuntos
Anticorpos Antibacterianos/imunologia , Antígenos de Bactérias/imunologia , Bacillus anthracis/imunologia , Toxinas Bacterianas/imunologia , Exotoxinas/imunologia , Animais , Anticorpos Monoclonais/biossíntese , Anticorpos Monoclonais/imunologia , Anticorpos Monoclonais/isolamento & purificação , Linhagem Celular , Mapeamento de Epitopos , Fragmentos Fc das Imunoglobulinas/imunologia , Camundongos
3.
Mol Gen Mikrobiol Virusol ; (3): 21-6, 2004.
Artigo em Russo | MEDLINE | ID: mdl-15354937

RESUMO

Anthrax belongs to highly dangerous infections of man and animals. No effective treatment methods for pulmonary types of the disease have been yet developed. The existing anthrax vaccines were designed decades ago and need improvement to fit the large-scale vaccination of population. At the same time, the immunological properties of the anthrax vaccine main component, i.e. of the protective agent, have been poorly studied. We obtained, within the present case study, a panel of mouse monoclonal antibodies to the protective agent and investigated the properties of the highest-affine panel representatives. An unusual phenomenon was detected, which is related with enhancement of the anthrax toxin action on the mouse macrophage-like cell-line in presence of the 1F2 monoclonal antibody. The remaining analyzed antibodies, i.e. 6G8 and 6G7, were found to neutralize effectively the toxin action. The enhancing and neutralizing antibodies were proven to be specific to different domains of the protective antigen and to recognize epitopes in its composition. The antibody-mediated enhancement of the anthrax lethal action is a convincing argument for further development of a new-generation anthrax vaccine. Definition of the linear antigen determinants for neutralizing antibodies in the protective antigens is an important step in the development of the next-generation anthrax vaccine.


Assuntos
Vacinas contra Antraz/imunologia , Anticorpos Monoclonais/imunologia , Antígenos de Bactérias/imunologia , Bacillus anthracis , Toxinas Bacterianas/imunologia , Animais , Vacinas contra Antraz/farmacologia , Anticorpos Antibacterianos/imunologia , Antígenos de Bactérias/farmacologia , Toxinas Bacterianas/farmacologia , Linhagem Celular , Epitopos/imunologia , Macrófagos/virologia , Camundongos , Camundongos Endogâmicos BALB C , Testes de Neutralização
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