Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/38663
Title: In Vivo Approaches Reveal a Key Role for DCs in CD4+T Cell Activation and Parasite Clearance during the Acute Phase of Experimental Blood-Stage Malaria
Authors: Silva, Henrique Borges da
Fonseca, Raissa
Cassado, Alexandra dos Anjos
Salles, Erika Machado de
Menezes, Maria Nogueira de
Langhorne, Jean
Perez, Katia Regina [UNIFESP]
Cuccovia, Iolanda Midea
Ryffel, Bernhard
Barreto, Vasco M.
Farias Marinho, Claudio Romero
Boscardin, Silvia Beatriz
Alvarez, Jose Maria
D'Imperio-Lima, Maria Regina
Tadokoro, Carlos Eduardo
Universidade de São Paulo (USP)
Inst Gulbenkian Ciencias
Charing Cross Sunley Med Res Ctr
Universidade Federal de São Paulo (UNIFESP)
Univ Orleans
Issue Date: 1-Feb-2015
Publisher: Public Library Science
Citation: Plos Pathogens. San Francisco: Public Library Science, v. 11, n. 2, 24 p., 2015.
Abstract: Dendritic cells (DCs) are phagocytes that are highly specialized for antigen presentation. Heterogeneous populations of macrophages and DCs form a phagocyte network inside the red pulp (RP) of the spleen, which is a major site for the control of blood-borne infections such as malaria. However, the dynamics of splenic DCs during Plasmodium infections are poorly understood, limiting our knowledge regarding their protective role in malaria. Here, we used in vivo experimental approaches that enabled us to deplete or visualize DCs in order to clarify these issues. To elucidate the roles of DCs and marginal zone macrophages in the protection against blood-stage malaria, we infected DTx (diphtheria toxin)-treated C57BL/6. CD11c-DTR mice, as well as C57BL/6 mice treated with low doses of clodronate liposomes (CILip), with Plasmodium chabaudi AS (Pc) parasites. the first evidence suggesting that DCs could contribute directly to parasite clearance was an early effect of the DTx treatment, but not of the CILip treatment, in parasitemia control. DCs were also required for CD4+ T cell responses during infection. the phagocytosis of infected red blood cells (iRBCs) by splenic DCs was analyzed by confocal intravital microscopy, as well as by flow cytometry and immunofluorescence, at three distinct phases of Pc malaria: at the first encounter, at pre-crisis concomitant with parasitemia growth and at crisis when the parasitemia decline coincides with spleen closure. in vivo and ex vivo imaging of the spleen revealed that DCs actively phagocytize iRBCs and interact with CD4+ T cells both in T cell-rich areas and in the RP. Subcapsular RP DCs were highly efficient in the recognition and capture of iRBCs during pre-crisis, while complete DC maturation was only achieved during crisis. These findings indicate that, beyond their classical role in antigen presentation, DCs also contribute to the direct elimination of iRBCs during acute Plasmodium infection.
URI: http://repositorio.unifesp.br/handle/11600/38663
ISSN: 1553-7366
Other Identifiers: http://dx.doi.org/10.1371/journal.ppat.1004598
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