Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective
The leishmaniases constitute a group of parasitic diseases caused by species of the protozoan genus <i>Leishmania</i>. In humans it can present different clinical manifestations and are usually classified as cutaneous, mucocutaneous, and visceral (VL). Although the full range of parasite...
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doaj-976dd58ff7f84aec83a19c7ee5ccf38f2021-04-05T23:00:21ZengMDPI AGMicroorganisms2076-26072021-04-01975975910.3390/microorganisms9040759Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological PerspectiveAikaterini Poulaki0Evangelia-Theophano Piperaki1Michael Voulgarelis2Department of Pathophysiology, School of Medicine, National and Kapodistrian University of Athens, 115 27 Athens, GreeceDepartment of Microbiology, School of Medicine, National and Kapodistrian University of Athens, 115 27 Athens, GreeceDepartment of Pathophysiology, School of Medicine, National and Kapodistrian University of Athens, 115 27 Athens, GreeceThe leishmaniases constitute a group of parasitic diseases caused by species of the protozoan genus <i>Leishmania</i>. In humans it can present different clinical manifestations and are usually classified as cutaneous, mucocutaneous, and visceral (VL). Although the full range of parasite—host interactions remains unclear, recent advances are improving our comprehension of VL pathophysiology. In this review we explore the differences in VL immunobiology between the liver and the spleen, leading to contrasting infection outcomes in the two organs, specifically clearance of the parasite in the liver and failure of the spleen to contain the infection. Based on parasite biology and the mammalian immune response, we describe how hypoxia-inducible factor 1 (HIF1) and the PI3K/Akt pathway function as major determinants of the observed immune failure. We also summarize existing knowledge on pancytopenia in VL, as a direct effect of the parasite on bone marrow health and regenerative capacity. Finally, we speculate on the possible effect that manipulation by the parasite of the PI3K/Akt/HIF1 axis may have on the myelodysplastic (MDS) features observed in VL.https://www.mdpi.com/2076-2607/9/4/759leishmaniasisvisceral leishmaniasisimmunobiologyliverspleenmicroenvironment |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Aikaterini Poulaki Evangelia-Theophano Piperaki Michael Voulgarelis |
spellingShingle |
Aikaterini Poulaki Evangelia-Theophano Piperaki Michael Voulgarelis Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective Microorganisms leishmaniasis visceral leishmaniasis immunobiology liver spleen microenvironment |
author_facet |
Aikaterini Poulaki Evangelia-Theophano Piperaki Michael Voulgarelis |
author_sort |
Aikaterini Poulaki |
title |
Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective |
title_short |
Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective |
title_full |
Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective |
title_fullStr |
Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective |
title_full_unstemmed |
Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective |
title_sort |
effects of visceralising leishmania on the spleen, liver, and bone marrow: a pathophysiological perspective |
publisher |
MDPI AG |
series |
Microorganisms |
issn |
2076-2607 |
publishDate |
2021-04-01 |
description |
The leishmaniases constitute a group of parasitic diseases caused by species of the protozoan genus <i>Leishmania</i>. In humans it can present different clinical manifestations and are usually classified as cutaneous, mucocutaneous, and visceral (VL). Although the full range of parasite—host interactions remains unclear, recent advances are improving our comprehension of VL pathophysiology. In this review we explore the differences in VL immunobiology between the liver and the spleen, leading to contrasting infection outcomes in the two organs, specifically clearance of the parasite in the liver and failure of the spleen to contain the infection. Based on parasite biology and the mammalian immune response, we describe how hypoxia-inducible factor 1 (HIF1) and the PI3K/Akt pathway function as major determinants of the observed immune failure. We also summarize existing knowledge on pancytopenia in VL, as a direct effect of the parasite on bone marrow health and regenerative capacity. Finally, we speculate on the possible effect that manipulation by the parasite of the PI3K/Akt/HIF1 axis may have on the myelodysplastic (MDS) features observed in VL. |
topic |
leishmaniasis visceral leishmaniasis immunobiology liver spleen microenvironment |
url |
https://www.mdpi.com/2076-2607/9/4/759 |
work_keys_str_mv |
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