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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Monocyte-derived dendritic cells in malaria

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Author(s):
Hirako, Isabella C. [1, 2] ; Assis, Patricia A. [2] ; Galvao-Filho, Bruno [1] ; Luster, Andrew D. [3, 4] ; Antonellil, Lis R. V. [1] ; Gazzinelli, Ricardo T. [1, 2, 5]
Total Authors: 6
Affiliation:
[1] Fundacao Oswaldo Cruz Minas, BR-30190002 Belo Horizonte, MG - Brazil
[2] Univ Massachusetts, Med Sch, Worcester, MA 01605 - USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 - USA
[4] Harvard Med Sch, Boston, MA 02115 - USA
[5] Fundacao Oswaldo Cruz, Plataforma Med Translac, BR-14049900 Ribeirao Preto, SP - Brazil
Total Affiliations: 5
Document type: Review article
Source: Current Opinion in Microbiology; v. 52, p. 139-150, DEC 2019.
Web of Science Citations: 0
Abstract

The pathogenesis of malaria is a multifactorial syndrome associated with a deleterious inflammatory response that is responsible for many of the clinical manifestations. While dendritic cells (DCs) play a critical role in initiating acquired immunity and host resistance to infection, they also play a pathogenic role in inflammatory diseases. In our recent studies, we found in different rodent malaria models that the monocyte-derived DCs (MO-DCs) become, transiently, a main DC population in spleens and inflamed non-lymphoid organs. These studies suggest that acute infection with Plasmodium berghei promotes the differentiation of splenic monocytes into inflammatory monocytes (iMOs) and thereafter into MO-DCs that play a pathogenic role by promoting inflammation and tissue damage. The recruitment of MO-DCs to the lungs and brain are dependent on expression of CCR4 and CCR5, respectively, and expression of respective chemokine ligands in each organ. Once they reach the target organ the MO-DCs produce the CXCR3 ligands (CXCL9 and CXCL10), recruit CD8 T cells, and produce toxic metabolites that play an important role in the development of experimental cerebral malaria (ECM) and acute respiratory distress syndrome (ARDS). (AU)

FAPESP's process: 16/23618-8 - Immunological mechanisms of resistance and disease in malaria
Grantee:João Santana da Silva
Support Opportunities: Research Projects - Thematic Grants