- Poster presentation
- Open Access
An immunoproteomic approach reveals a different pattern of non-infected erythrocyte membrane protein recognition by antibodies from non-anemic and anemic patients with patent Plasmodium vivax infection
© Mourao et al; licensee BioMed Central Ltd. 2014
- Published: 22 September 2014
- Erythrocyte Membrane
- Anemic Patient
- Vivax Infection
- Plasmodium Vivax Infection
Anemia is a typical manifestation of Plasmodium vivax infection and one of the leading causes of morbidity and mortality, particularly in pregnant women and children less than five years old. Despite the magnitude of the problem, there remain major unsolved questions about its etiology. In this context, we have addressed the following question: Are antibodies directed to erythrocyte membrane proteins involved in the accelerated clearance of red blood cells (RBCs) by phagocytes leading to anemia during P. vivax infection? We performed immunoproteomic assays trying to characterize proteins that are targets of antibodies. Sera from four groups of subjects were tested against a non-infected O+ erythrocyte membrane extract and are included in our study: P. vivax anemic individuals (PvAN); P. vivax non-anemic individuals (PvNA); non-infected individuals with anemia by other etiologies (NIAN); and non-infected and non-anemic individuals (NINA). Immunoblots revealed a differential pattern of RBC protein recognition related to the four studied groups. The breadth and the magnitude of antibody responses against RBC membrane antigens were higher in NAPv and ANPv, corroborating our previous results obtained by ELISA and 1-D immunoblot. Now, these proteins are being identified by peptide mass fingerprint. Next, we will confirm their identity by MALDI TOF/MS-MS, validate and categorize them in relation to location, family and function. Highly immunogenic and differentially recognized proteins will represent potential candidates for diagnostic or prognostic biomarkers of anemia in P. vivax infections. Moreover, data generated here will contribute to the better understanding of mechanisms enrolled in vivax anemia pathogenesis.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.