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HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children
AIM: Cerebral malaria (CM), unlike severe malarial anemia (SMA), has previously been characterized by pan-lymphopenia that normalizes in convalescence, while HIV infection is associated with depletion of CD4(+) T cells. In this study, we investigate whether HIV infection in Malawian children exacerb...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305159/ https://www.ncbi.nlm.nih.gov/pubmed/30588141 http://dx.doi.org/10.2147/JBM.S187081 |
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author | Mandala, Wilson L Gondwe, Esther N Nyirenda, Tonney S Drayson, Mark Molyneux, Malcolm E MacLennan, Calman A |
author_facet | Mandala, Wilson L Gondwe, Esther N Nyirenda, Tonney S Drayson, Mark Molyneux, Malcolm E MacLennan, Calman A |
author_sort | Mandala, Wilson L |
collection | PubMed |
description | AIM: Cerebral malaria (CM), unlike severe malarial anemia (SMA), has previously been characterized by pan-lymphopenia that normalizes in convalescence, while HIV infection is associated with depletion of CD4(+) T cells. In this study, we investigate whether HIV infection in Malawian children exacerbates the pan-lymphopenia associated with CM. METHODS: We investigated the absolute and percentage lymphocyte-subset counts and their activation and memory status in Malawian children presenting with either CM who were HIV-uninfected (n=29), HIV-infected (n=9), or SMA who were HIV-uninfected (n=30) and HIV-infected (n=5) in comparison with HIV-uninfected children without malaria (n=42) and HIV-infected children without malaria (n=4). RESULTS: HIV-infected CM cases had significantly lower absolute counts of T cells (P=0.006), CD4(+) T cells (P=0.0008), and B cells (P=0.0014) than HIV-uninfected CM cases, and significantly lower percentages of CD4(+) T cells than HIV-uninfected CM cases (P=0.005). HIV-infected SMA cases had significantly lower percentages of CD4(+) T cells (P=0.001) and higher CD8(+) T cells (P=0.003) in comparison with HIV-uninfected SMA cases. HIV-infected SMA cases had higher proportions of activated T cells (P=0.003) expressing CD69 than HIV-uninfected SMA cases. CONCLUSION: HIV infection compounds the perturbation of acute CM and SMA on lymphocytes, exacerbating subset-specific lymphopenia in CM and increasing activation status in SMA, potentially exacerbating host immunocompromise. |
format | Online Article Text |
id | pubmed-6305159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63051592018-12-26 HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children Mandala, Wilson L Gondwe, Esther N Nyirenda, Tonney S Drayson, Mark Molyneux, Malcolm E MacLennan, Calman A J Blood Med Original Research AIM: Cerebral malaria (CM), unlike severe malarial anemia (SMA), has previously been characterized by pan-lymphopenia that normalizes in convalescence, while HIV infection is associated with depletion of CD4(+) T cells. In this study, we investigate whether HIV infection in Malawian children exacerbates the pan-lymphopenia associated with CM. METHODS: We investigated the absolute and percentage lymphocyte-subset counts and their activation and memory status in Malawian children presenting with either CM who were HIV-uninfected (n=29), HIV-infected (n=9), or SMA who were HIV-uninfected (n=30) and HIV-infected (n=5) in comparison with HIV-uninfected children without malaria (n=42) and HIV-infected children without malaria (n=4). RESULTS: HIV-infected CM cases had significantly lower absolute counts of T cells (P=0.006), CD4(+) T cells (P=0.0008), and B cells (P=0.0014) than HIV-uninfected CM cases, and significantly lower percentages of CD4(+) T cells than HIV-uninfected CM cases (P=0.005). HIV-infected SMA cases had significantly lower percentages of CD4(+) T cells (P=0.001) and higher CD8(+) T cells (P=0.003) in comparison with HIV-uninfected SMA cases. HIV-infected SMA cases had higher proportions of activated T cells (P=0.003) expressing CD69 than HIV-uninfected SMA cases. CONCLUSION: HIV infection compounds the perturbation of acute CM and SMA on lymphocytes, exacerbating subset-specific lymphopenia in CM and increasing activation status in SMA, potentially exacerbating host immunocompromise. Dove Medical Press 2018-12-19 /pmc/articles/PMC6305159/ /pubmed/30588141 http://dx.doi.org/10.2147/JBM.S187081 Text en © 2019 Mandala et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Mandala, Wilson L Gondwe, Esther N Nyirenda, Tonney S Drayson, Mark Molyneux, Malcolm E MacLennan, Calman A HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children |
title | HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children |
title_full | HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children |
title_fullStr | HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children |
title_full_unstemmed | HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children |
title_short | HIV infection compounds the lymphopenia associated with cerebral malaria in Malawian children |
title_sort | hiv infection compounds the lymphopenia associated with cerebral malaria in malawian children |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305159/ https://www.ncbi.nlm.nih.gov/pubmed/30588141 http://dx.doi.org/10.2147/JBM.S187081 |
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