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1.
Infect Immun ; 74(10): 5933-42, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16988273

RESUMO

The safety, immunogenicity, and efficacy of DNA and modified vaccinia virus Ankara (MVA) prime-boost regimes were assessed by using either thrombospondin-related adhesion protein (TRAP) with a multiple-epitope string ME (ME-TRAP) or the circumsporozoite protein (CS) of Plasmodium falciparum. Sixteen healthy subjects who never had malaria (malaria-naive subjects) received two priming vaccinations with DNA, followed by one boosting immunization with MVA, with either ME-TRAP or CS as the antigen. Immunogenicity was assessed by ex vivo gamma interferon (IFN-gamma) enzyme-linked immunospot assay (ELISPOT) and antibody assay. Two weeks after the final vaccination, the subjects underwent P. falciparum sporozoite challenge, with six unvaccinated controls. The vaccines were well tolerated and immunogenic, with the DDM-ME TRAP regimen producing stronger ex vivo IFN-gamma ELISPOT responses than DDM-CS. One of eight subjects receiving the DDM-ME TRAP regimen was completely protected against malaria challenge, with this group as a whole showing significant delay to parasitemia compared to controls (P = 0.045). The peak ex vivo IFN-gamma ELISPOT response in this group correlated strongly with the number of days to parasitemia (P = 0.033). No protection was observed in the DDM-CS group. Prime-boost vaccination with DNA and MVA encoding ME-TRAP but not CS resulted in partial protection against P. falciparum sporozoite challenge in the present study.


Assuntos
Vacinas Antimaláricas/uso terapêutico , Malária Falciparum/prevenção & controle , Plasmodium falciparum , Proteínas de Protozoários/imunologia , Vaccinia virus/genética , Adolescente , Adulto , Animais , Anticorpos Antiprotozoários/sangue , Feminino , Humanos , Imunização Secundária , Interferon gama/sangue , Vacinas Antimaláricas/imunologia , Masculino , Pessoa de Meia-Idade , Proteínas de Protozoários/genética , Vacinas de DNA/imunologia , Vacinas de DNA/uso terapêutico , Proteínas Virais/genética
2.
Trans R Soc Trop Med Hyg ; 91(3): 319-21, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9231208

RESUMO

Primary data were collected on the incidence, severity and species responsible for snake bites in 4 areas of Kenya: (i) Kakamega and western Kenya, (ii) Lake Baringo and Laikipia, (iii) Kilifi and Malindi, and (iv) northern Kenya. The overall average frequency of snake bite was 13.8 per 100,000 population per year (range 1.9-67.9). The minimum rate of snake bite mortality was 0.45/100,000/year. Thirty-four of the 50 units visited reported no knowledge of death from snake bite in the last 5 years. Possible reasons for the low estimates are discussed. Traditional treatments were common, especially the use of herbal remedies and incisions at the wound site.


Assuntos
Mordeduras de Serpentes/epidemiologia , Antivenenos/uso terapêutico , Humanos , Incidência , Quênia/epidemiologia , Mordeduras de Serpentes/terapia
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