Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/16305
Título: Anti-Anopheles darlingi saliva antibodies as marker of Plasmodium vivax infection and clinical immunity in the Brazilian Amazon
Autor: Andrade, Bruno B.
Rocha, Bruno Coelho
Reis-Filho, Antonio
Camargo, Luis Marcelo Aranha
Tadei, Wanderli Pedro
Moreira, Luciano Andrade
Barral, Aldina Maria Prado
Barral-Netto, M.
Palavras-chave: Darlingi Saliva Gland Sonicate Antibody
Gamma Interferon
Interleukin-10
Protozoon Antibody
Unclassified Drug
Antibody
Biological Marker
Gamma Interferon
Insect Proteins
Interleukin-10
Adult
Antibody Blood Level
Antibody Titer
Blood Sampling
Concentration (parameters)
Control Group
Controlled Study
Cytokine Production
Disease Severity
Female
Human
Humoral Immunity
Immunity
Major Clinical Study
Microscopy
Parasitemia
Plasmodium Vivax
Plasmodium Vivax Malaria
Polymerase Chain Reaction
Screening
Animals
Anopheles
Blood
Immunology
Middle Aged
Plasmodium Vivax Malaria
Prediction And Forecasting
Saliva
Adult
Animal
Anopheles
Antibodies
Biological Markers
Female
Humans
Insect Proteins
Interferon-gamma
Interleukin-10
Malaria, Vivax
Middle Aged
Predictive Value Of Tests
Saliva
Young Adult
Data do documento: 2009
Revista: Malaria Journal
É parte de: Volume 8, Número 1
Abstract: Background. Despite governmental and private efforts on providing malaria control, this disease continues to be a major health threat. Thus, innovative strategies are needed to reduce disease burden. The malaria vectors, through the injection of saliva into the host skin, play important role on disease transmission and may influence malaria morbidity. This study describes the humoral immune response against Anopheles (An.) darlingi saliva in volunteers from the Brazilian Amazon and addresses the association between levels of specific antibodies and clinical presentation of Plasmodium (P.) vivax infection. Methods. Adult volunteers from communities in the Rondônia State, Brazil, were screened in order to assess the presence of P. vivax infection by light microscopy and nested PCR. Non-infected volunteers and individuals with symptomatic or symptomless infection were randomly selected and plasma collected. An. darlingi salivary gland sonicates (SGS) were prepared and used to measure anti-saliva antibody levels. Plasma interleukin (IL)-10 and interferon (IFN)- levels were also estimated and correlated to anti-SGS levels. Results. Individuals infected with P. vivax presented higher levels of anti-SGS than non-infected individuals and antibody levels could discriminate infection. Furthermore, anti-saliva antibody measurement was also useful to distinguish asymptomatic infection from non-infection, with a high likelihood ratio. Interestingly, individuals with asymptomatic parasitaemia presented higher titers of anti-SGS and lower IFN-/IL-10 ratio than symptomatic ones. In P. vivax-infected asymptomatic individuals, the IFN-/IL-10 ratio was inversely correlated to anti-SGS titers, although not for while in symptomatic volunteers. Conclusion. The estimation of anti-An. darlingi antibody levels can indicate the probable P. vivax infection status and also could serve as a marker of disease severity in this region of Brazilian Amazon. © 2009 Andrade et al; licensee BioMed Central Ltd.
DOI: 10.1186/1475-2875-8-121
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