Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice

Background: Inflammation is a crucial process driving pathogenesis in malaria infection. The devastating effects of malaria infection has always been associated with severe inflammation whilst protective effect is linked to provocation of anti-inflammation responses. IL-4, IL-10 and IL-13 are well-e...

Full description

Bibliographic Details
Main Authors: Chin, V. K., Chong, W. C., H., Haniza, Basir, R.
Format: Article
Published: Faculty of Medicine, University of Malaya 2021
Online Access:http://psasir.upm.edu.my/id/eprint/94239/
_version_ 1848861944170151936
author Chin, V. K.
Chong, W. C.
H., Haniza
Basir, R.
author_facet Chin, V. K.
Chong, W. C.
H., Haniza
Basir, R.
author_sort Chin, V. K.
building UPM Institutional Repository
collection Online Access
description Background: Inflammation is a crucial process driving pathogenesis in malaria infection. The devastating effects of malaria infection has always been associated with severe inflammation whilst protective effect is linked to provocation of anti-inflammation responses. IL-4, IL-10 and IL-13 are well-established anti-inflammatory cytokines with their functional roles during malaria infection remain elusive. Therefore, this study was undertaken to study the effects of modulating IL-10, IL-4 and IL-13 on the course of malaria infection in Plasmodium berghei ANKA (PbA)-infected murine model. Methods: Male ICR mice were randomly assigned into 5 different groupings and were infected intraperitoneal with 0.2 mL of 2 x 107 pRBCs containing P. berghei ANKA (PbA). Malaria-infected mice were treated with recombinant mouse IL-4 (rmIL-4), recombinant mouse IL-10 (rmIL-10) and recombinant mouse IL-13 (rmIL-13) for 4 consecutive days after the establishment of the infection. The survival and parasitemia levels of malarial mice and malarial mice under different treatments were monitored. Major affected organs (kidneys, lungs, brain, liver and spleen) were subjected to histopathological analysis at day-5 post infection. Results: Our findings revealed that the overall lifespan of malarial mice treated with recombinant mouse rmIL10, rmIL-4 and rmIL-13 were prolonged, accompanied with significant reduction in malaria parasitemia levels, in particular in malarial mice receiving recombinant rmIL-10 and rmIL-13. Histopathological conditions of kidneys, lungs, brain, liver and spleen treated with recombinant mouse rmIL-10, rmIL-4 and rmIL-13 were also improved. Sequestration of parasitized red blood cells (pRBCs) and inflammation seen in major affected organs were alleviated. Conclusion: Despite some limitations, this preliminary study demonstrated the promising therapeutic effects of IL-10 and IL-13 as adjuvant therapies in reducing severe pathological manifestations triggered by inflammation during malaria infection.
first_indexed 2025-11-15T13:09:10Z
format Article
id upm-94239
institution Universiti Putra Malaysia
institution_category Local University
last_indexed 2025-11-15T13:09:10Z
publishDate 2021
publisher Faculty of Medicine, University of Malaya
recordtype eprints
repository_type Digital Repository
spelling upm-942392023-05-09T01:53:05Z http://psasir.upm.edu.my/id/eprint/94239/ Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice Chin, V. K. Chong, W. C. H., Haniza Basir, R. Background: Inflammation is a crucial process driving pathogenesis in malaria infection. The devastating effects of malaria infection has always been associated with severe inflammation whilst protective effect is linked to provocation of anti-inflammation responses. IL-4, IL-10 and IL-13 are well-established anti-inflammatory cytokines with their functional roles during malaria infection remain elusive. Therefore, this study was undertaken to study the effects of modulating IL-10, IL-4 and IL-13 on the course of malaria infection in Plasmodium berghei ANKA (PbA)-infected murine model. Methods: Male ICR mice were randomly assigned into 5 different groupings and were infected intraperitoneal with 0.2 mL of 2 x 107 pRBCs containing P. berghei ANKA (PbA). Malaria-infected mice were treated with recombinant mouse IL-4 (rmIL-4), recombinant mouse IL-10 (rmIL-10) and recombinant mouse IL-13 (rmIL-13) for 4 consecutive days after the establishment of the infection. The survival and parasitemia levels of malarial mice and malarial mice under different treatments were monitored. Major affected organs (kidneys, lungs, brain, liver and spleen) were subjected to histopathological analysis at day-5 post infection. Results: Our findings revealed that the overall lifespan of malarial mice treated with recombinant mouse rmIL10, rmIL-4 and rmIL-13 were prolonged, accompanied with significant reduction in malaria parasitemia levels, in particular in malarial mice receiving recombinant rmIL-10 and rmIL-13. Histopathological conditions of kidneys, lungs, brain, liver and spleen treated with recombinant mouse rmIL-10, rmIL-4 and rmIL-13 were also improved. Sequestration of parasitized red blood cells (pRBCs) and inflammation seen in major affected organs were alleviated. Conclusion: Despite some limitations, this preliminary study demonstrated the promising therapeutic effects of IL-10 and IL-13 as adjuvant therapies in reducing severe pathological manifestations triggered by inflammation during malaria infection. Faculty of Medicine, University of Malaya 2021-10-07 Article PeerReviewed Chin, V. K. and Chong, W. C. and H., Haniza and Basir, R. (2021) Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice. Journal of Health and Translational Medicine (JUMMEC), 24 (2). 92 - 105. ISSN 1823-7339; ESSN: 2289-392X https://jummec.um.edu.my/index.php/jummec/article/view/21991 10.22452/jummec.vol24no2.13
spellingShingle Chin, V. K.
Chong, W. C.
H., Haniza
Basir, R.
Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice
title Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice
title_full Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice
title_fullStr Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice
title_full_unstemmed Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice
title_short Modulating effects of IL-4, IL-10 AND IL-13 on the course of Plasmodium berghei malaria infection in mice
title_sort modulating effects of il-4, il-10 and il-13 on the course of plasmodium berghei malaria infection in mice
url http://psasir.upm.edu.my/id/eprint/94239/
http://psasir.upm.edu.my/id/eprint/94239/
http://psasir.upm.edu.my/id/eprint/94239/