Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum

To a considerable degree, malaria-induced immunosuppression has been attributed to an inhibition of macrophage accessory cell function. In this study hemozoin, a plasmodium hemoglobin degradation product which readily accumulates in phagocytic cells and tissues during infection, was examined for its...

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Main Authors: Morakote N., Justus DE.
Format: Article
Language:English
Published: 2014
Online Access:http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3586
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-35862014-08-30T02:35:04Z Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum Morakote N. Justus DE. To a considerable degree, malaria-induced immunosuppression has been attributed to an inhibition of macrophage accessory cell function. In this study hemozoin, a plasmodium hemoglobin degradation product which readily accumulates in phagocytic cells and tissues during infection, was examined for its influence on immune responses. Hemozoin-laden liver and splenic macrophages from Plasmodium berghei-infected mice, displayed accessory cell dysfunction which was likely due to hemozoin loading by these phagocytic cells. This indicated by the observation that hemozoin obtained from livers and spleens of infected mice as well as from Plasmodium falciparum cultures greatly inhibited splenic plaque-forming cell responses to sheep red blood cells. The results of the present study strongly suggest that the inhibition of macrophage accessory cell activity is due, at least in part, to the uptake and accumulation of hemozoin in their cytoplasms. 2014-08-30T02:35:04Z 2014-08-30T02:35:04Z 1988 Journal Article 0020-5915 3286520 http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3586 eng
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description To a considerable degree, malaria-induced immunosuppression has been attributed to an inhibition of macrophage accessory cell function. In this study hemozoin, a plasmodium hemoglobin degradation product which readily accumulates in phagocytic cells and tissues during infection, was examined for its influence on immune responses. Hemozoin-laden liver and splenic macrophages from Plasmodium berghei-infected mice, displayed accessory cell dysfunction which was likely due to hemozoin loading by these phagocytic cells. This indicated by the observation that hemozoin obtained from livers and spleens of infected mice as well as from Plasmodium falciparum cultures greatly inhibited splenic plaque-forming cell responses to sheep red blood cells. The results of the present study strongly suggest that the inhibition of macrophage accessory cell activity is due, at least in part, to the uptake and accumulation of hemozoin in their cytoplasms.
format Article
author Morakote N.
Justus DE.
spellingShingle Morakote N.
Justus DE.
Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum
author_facet Morakote N.
Justus DE.
author_sort Morakote N.
title Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum
title_short Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum
title_full Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum
title_fullStr Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum
title_full_unstemmed Immunosuppression in malaria: effect of hemozoin produced by Plasmodium berghei and Plasmodium falciparum
title_sort immunosuppression in malaria: effect of hemozoin produced by plasmodium berghei and plasmodium falciparum
publishDate 2014
url http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3586
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