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Acute lung injury is prevented by monocyte locomotion inhibitory factor in an experimental severe malaria mouse model.
- Source :
-
Immunobiology [Immunobiology] 2024 Jul; Vol. 229 (4), pp. 152823. Date of Electronic Publication: 2024 Jun 06. - Publication Year :
- 2024
-
Abstract
- Acute lung injury caused by severe malaria (SM) is triggered by a dysregulated immune response towards the infection with Plasmodium parasites. Postmortem analysis of human lungs shows diffuse alveolar damage (DAD), the presence of CD8 lymphocytes, neutrophils, and increased expression of Intercellular Adhesion Molecule 1 (ICAM-1). P. berghei ANKA (PbA) infection in C57BL/6 mice reproduces many SM features, including acute lung injury characterized by DAD, CD8 <superscript>+</superscript> T lymphocytes and neutrophils in the lung parenchyma, and tissular expression of proinflammatory cytokines and adhesion molecules, such as IFNγ, TNFα, ICAM, and VCAM. Since this is related to a dysregulated immune response, immunomodulatory agents are proposed to reduce the complications of SM. The monocyte locomotion inhibitory factor (MLIF) is an immunomodulatory pentapeptide isolated from axenic cultures of Entamoeba hystolitica. Thus, we evaluated if the MLIF intraperitoneal (i.p.) treatment prevented SM-induced acute lung injury. The peptide prevented SM without a parasiticidal effect, indicating that its protective effect was related to modifications in the immune response. Furthermore, peripheral CD8 <superscript>+</superscript> leukocytes and neutrophil proportions were higher in infected treated mice. However, the treatment prevented DAD, CD8 <superscript>+</superscript> cell infiltration into the pulmonary tissue and downregulated IFNγ. Moreover, VCAM-1 expression was abrogated. These results indicate that the MLIF treatment downregulated adhesion molecule expression, impeding cell migration and proinflammatory cytokine tissular production, preventing acute lung injury induced by SM. Our findings represent a potential novel strategy to avoid this complication in various events where a dysregulated immune response triggers lung injury.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Authors. Published by Elsevier GmbH.. All rights reserved.)
- Subjects :
- Animals
Mice
Mice, Inbred C57BL
Neutrophils immunology
CD8-Positive T-Lymphocytes immunology
Cytokines metabolism
Lung immunology
Lung pathology
Humans
Female
Oligopeptides
Acute Lung Injury immunology
Acute Lung Injury etiology
Disease Models, Animal
Malaria immunology
Plasmodium berghei immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1878-3279
- Volume :
- 229
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Immunobiology
- Publication Type :
- Academic Journal
- Accession number :
- 38861873
- Full Text :
- https://doi.org/10.1016/j.imbio.2024.152823