Macrophage Mediated Immunomodulation During Cryptococcus Pulmonary Infection

Macrophages are key cellular components of innate immunity, acting as the first line of defense against pathogens to modulate homeostatic and inflammatory responses. They help clear pathogens and shape the T-cell response through the production of cytokines and chemokines. The facultative intracellu...

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Published inFrontiers in cellular and infection microbiology Vol. 12; p. 859049
Main Authors Wang, Yan, Pawar, Siddhi, Dutta, Orchi, Wang, Keyi, Rivera, Amariliz, Xue, Chaoyang
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 24.03.2022
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Summary:Macrophages are key cellular components of innate immunity, acting as the first line of defense against pathogens to modulate homeostatic and inflammatory responses. They help clear pathogens and shape the T-cell response through the production of cytokines and chemokines. The facultative intracellular fungal pathogen has developed a unique ability to interact with and manipulate host macrophages. These interactions dictate how infection can remain latent or how dissemination within the host is achieved. In addition, differences in the activities of macrophages have been correlated with differential susceptibilities of hosts to infection, highlighting the importance of macrophages in determining disease outcomes. There is now abundant information on the interaction between and macrophages. In this review we discuss recent advances regarding macrophage origin, polarization, activation, and effector functions during infection. The importance of these strategies in pathogenesis and the potential of immunotherapy for cryptococcosis treatment is also discussed.
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Reviewed by: Carolina Coelho, University of Exeter, United Kingdom; Emma Camacho, Johns Hopkins University, United States
Edited by: James Kronstad, University of British Columbia, Canada
This article was submitted to Fungal Pathogenesis, a section of the journal Frontiers in Cellular and Infection Microbiology
ISSN:2235-2988
2235-2988
DOI:10.3389/fcimb.2022.859049