cris.boxmetadata.label.title
Diagnostic evaluation of the amastin protein from Leishmania infantum in canine and human visceral leishmaniasis and immunogenicity in human cells derived from patients and healthy controls
cris.boxmetadata.label.dateissued
01 browse.startsWith.months.october 2019
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Vale D.
Dias D.
Machado A.
Ribeiro P.
Lage D.
Costa L.
Steiner B.
Tavares G.
Ramos F.
Martínez-Rodrigo A.
CHAVEZ FUMAGALLI, MIGUEL ANGEL
Caligiorne R.
de Magalhães-Soares D.
Silveira J.
Machado-de-Ávila R.
Teixeira A.
Coelho E.
cris.boxmetadata.label.publisher
Elsevier Inc.
cris.boxmetadata.label.abstract
The diagnosis of visceral leishmaniasis (VL) presents problems due to the toxicity and/or high cost of drugs. In addition, no vaccine exists to protect against human disease. In this study, the antigenicity and immunogenicity of amastin protein were evaluated in L. infantum–infected dogs and humans. For the diagnosis, besides the recombinant protein, 1 linear B-cell epitope was synthetized and evaluated in serological assays. Results showed high sensitivity and specificity values to detect the disease when both antigens were employed against a canine and human serological panel. By contrast, when using rA2 and a soluble Leishmania antigenic preparation, sensitivity and specificity values proved to be lower. A preliminary immunogenicity study showed that the amastin protein induced high IFN-γ and low IL-10 production in stimulated PBMC derived from treated VL patients and healthy subjects, thus suggesting a potential use of this protein as an immunogen to protect against human disease.
cris.boxmetadata.label.citationstartpage
134
cris.boxmetadata.label.citationendpage
143
cris.boxmetadata.label.volume
95
cris.boxmetadata.label.issue
2
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Inmunología Enfermedades infecciosas Biología celular, Microbiología
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-85066237484
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Diagnostic Microbiology and Infectious Disease
cris.boxmetadata.label.containerissn
07328893
cris.boxmetadata.label.sponsor
The authors would like thank to CAPES, CNPq, and FAPEMIG for the scholarships. This work was supported by grants from CNPq ( APQ-408675/2018-7 ).
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