Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria

Secondary lymphoid tissues play a major role in the human immune response to <i>P. falciparum</i> infection. Previous studies have shown that acute falciparum malaria is associated with marked perturbations of the cellular immune system characterized by lowered frequency and absolute num...

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Main Authors: Wilson L. Mandala, Steve Ward, Terrie E. Taylor, Samuel C. Wassmer
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Pathogens
Subjects:
Online Access:https://www.mdpi.com/2076-0817/11/8/851
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author Wilson L. Mandala
Steve Ward
Terrie E. Taylor
Samuel C. Wassmer
author_facet Wilson L. Mandala
Steve Ward
Terrie E. Taylor
Samuel C. Wassmer
author_sort Wilson L. Mandala
collection DOAJ
description Secondary lymphoid tissues play a major role in the human immune response to <i>P. falciparum</i> infection. Previous studies have shown that acute falciparum malaria is associated with marked perturbations of the cellular immune system characterized by lowered frequency and absolute number of circulating T cell subsets. A temporary relocation of T cells, possibly by infiltration to secondary lymphoid tissue, or their permanent loss through apoptosis, are two proposed explanations for this observation. We conducted the present study to determine the phenotype of lymphocyte subsets that accumulate in the lymph node and spleen during acute stages of falciparum malaria infection in Malawian children, and to test the hypothesis that lymphocytes are relocated to lymphoid tissues during acute infection. We stained tissue sections from children who had died of the two common clinical forms of severe malaria in Malawi, namely severe malarial anemia (SMA, n = 1) and cerebral malaria (CM, n = 3), and used tissue sections from pediatric patients who had died of non-malaria sepsis (n = 2) as controls. Both lymph node and spleen tissue (red pulp) sections from CM patients had higher percentages of T cells (CD4<sup>+</sup> and CD8<sup>+</sup>) compared to the SMA patient. In the latter, we observed a higher percentage of CD20<sup>+</sup> B cells in the lymph nodes compared to CM patients, whereas the opposite was observed in the spleen. Both lymph node and spleen sections from CM patients had increased percentages of CD69<sup>+</sup> and CD45RO<sup>+</sup> cells compared to tissue sections from the SMA patient. These results support the hypothesis that the relocation of lymphocytes to spleen and lymph node may contribute to the pan-lymphopenia observed in acute CM.
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spelling doaj.art-09adcd165bd64e2f9ac19443ceb797162023-12-03T14:15:18ZengMDPI AGPathogens2076-08172022-07-0111885110.3390/pathogens11080851Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric MalariaWilson L. Mandala0Steve Ward1Terrie E. Taylor2Samuel C. Wassmer3Academy of Medical Sciences, Malawi University of Science and Technology, Thyolo 310106, MalawiDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool L3 5QA, UKBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre 312233, MalawiMalawi Liverpool Wellcome Trust Clinical Research Programme, Blantyre 312233, MalawiSecondary lymphoid tissues play a major role in the human immune response to <i>P. falciparum</i> infection. Previous studies have shown that acute falciparum malaria is associated with marked perturbations of the cellular immune system characterized by lowered frequency and absolute number of circulating T cell subsets. A temporary relocation of T cells, possibly by infiltration to secondary lymphoid tissue, or their permanent loss through apoptosis, are two proposed explanations for this observation. We conducted the present study to determine the phenotype of lymphocyte subsets that accumulate in the lymph node and spleen during acute stages of falciparum malaria infection in Malawian children, and to test the hypothesis that lymphocytes are relocated to lymphoid tissues during acute infection. We stained tissue sections from children who had died of the two common clinical forms of severe malaria in Malawi, namely severe malarial anemia (SMA, n = 1) and cerebral malaria (CM, n = 3), and used tissue sections from pediatric patients who had died of non-malaria sepsis (n = 2) as controls. Both lymph node and spleen tissue (red pulp) sections from CM patients had higher percentages of T cells (CD4<sup>+</sup> and CD8<sup>+</sup>) compared to the SMA patient. In the latter, we observed a higher percentage of CD20<sup>+</sup> B cells in the lymph nodes compared to CM patients, whereas the opposite was observed in the spleen. Both lymph node and spleen sections from CM patients had increased percentages of CD69<sup>+</sup> and CD45RO<sup>+</sup> cells compared to tissue sections from the SMA patient. These results support the hypothesis that the relocation of lymphocytes to spleen and lymph node may contribute to the pan-lymphopenia observed in acute CM.https://www.mdpi.com/2076-0817/11/8/851<i>P. falciparum</i> malarialymphocyteslymph nodesspleen
spellingShingle Wilson L. Mandala
Steve Ward
Terrie E. Taylor
Samuel C. Wassmer
Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria
Pathogens
<i>P. falciparum</i> malaria
lymphocytes
lymph nodes
spleen
title Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria
title_full Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria
title_fullStr Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria
title_full_unstemmed Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria
title_short Characterization of Lymphocyte Subsets in Lymph Node and Spleen Sections in Fatal Pediatric Malaria
title_sort characterization of lymphocyte subsets in lymph node and spleen sections in fatal pediatric malaria
topic <i>P. falciparum</i> malaria
lymphocytes
lymph nodes
spleen
url https://www.mdpi.com/2076-0817/11/8/851
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AT steveward characterizationoflymphocytesubsetsinlymphnodeandspleensectionsinfatalpediatricmalaria
AT terrieetaylor characterizationoflymphocytesubsetsinlymphnodeandspleensectionsinfatalpediatricmalaria
AT samuelcwassmer characterizationoflymphocytesubsetsinlymphnodeandspleensectionsinfatalpediatricmalaria