Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/104551
Title: Spleen-Dependent Immune Protection Elicited by CpG Adjuvanted Reticulocyte-Derived Exosomes from Malaria Infection Is Associated with Changes in T cell Subsets' Distribution
Author: Martín Jaular, Lorena
Menezes Neto, Armando de
Monguió Tortajada, Marta
Elizalde Torrent, Aleix
Díaz Varela, Míriam
Fernández Becerra, Carmen
Borràs, Francesc E.
Montoya, Maria
Portillo Obando, Hernando A. del
Keywords: Malària
Cèl·lules T
Malaria
T cells
Issue Date: 16-Nov-2016
Publisher: Frontiers Media
Abstract: Reticulocyte-derived exosomes (rex) are 30-100 nm membrane vesicles of endocytic origin released during the maturation of reticulocytes to erythrocytes upon fusion of multivesicular bodies with the plasma membrane. Combination of CpG-ODN with rex obtained from BALB/c mice infected with the reticulocyte-prone non-lethal P. yoelii 17X malaria strain (rexPy), had been shown to induce survival and long lasting protection. Here, we show that splenectomized mice are not protected upon rexPy+CpG inmunizations and that protection is restored upon passive transfer of splenocytes obtained from animals immunized with rexPy+CpG. Notably, rexPy immunization of mice induced changes in PD1- memory T cells with effector phenotype. Proteomics analysis of rexPy confirmed their reticulocyte origin and demonstrated the presence of parasite antigens. Our studies thus prove, for what we believe is the first time, that rex from reticulocyte-prone malarial infections are associated with splenic long-lasting memory responses. To try extrapolating these data to human infections, in vitro experiments with spleen cells of human transplantation donors were performed. Plasma-derived exosomes from vivax malaria patients (exPv) were actively uptaken by human splenocytes and stimulated spleen cells leading to changes in T cell subsets.
Note: Added corrigendum published in 2017-01-17 https://doi.org/10.3389/fcell.2016.00153
Note: Reproducció del document publicat a: http://dx.doi.org/10.3389/fcell.2016.00131
It is part of: Frontiers in Cell and Developmental Biology, 2016, vol. 4, p. 131
Related resource: http://dx.doi.org/10.3389/fcell.2016.00131
URI: http://hdl.handle.net/2445/104551
ISSN: 2296-634X
Appears in Collections:Articles publicats en revistes (ISGlobal)

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