Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children
Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenot...
Ausführliche Beschreibung
Autor*in: |
Asito, Amolo S [verfasserIn] |
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Englisch |
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2008 |
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© Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
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Übergeordnetes Werk: |
Enthalten in: Malaria journal - London : BioMed Central, 2002, 7(2008), 1 vom: 18. Nov. |
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Übergeordnetes Werk: |
volume:7 ; year:2008 ; number:1 ; day:18 ; month:11 |
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DOI / URN: |
10.1186/1475-2875-7-238 |
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SPR028603915 |
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245 | 1 | 0 | |a Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children |
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520 | |a Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. | ||
650 | 4 | |a Malaria |7 (dpeaa)DE-He213 | |
650 | 4 | |a Peripheral Blood Mononuclear Cell |7 (dpeaa)DE-He213 | |
650 | 4 | |a Cell Subset |7 (dpeaa)DE-He213 | |
650 | 4 | |a Falciparum Malaria |7 (dpeaa)DE-He213 | |
650 | 4 | |a Burkitt Lymphoma |7 (dpeaa)DE-He213 | |
700 | 1 | |a Moormann, Ann M |4 aut | |
700 | 1 | |a Kiprotich, Chelimo |4 aut | |
700 | 1 | |a Ng'ang'a, Zipporah W |4 aut | |
700 | 1 | |a Ploutz-Snyder, Robert |4 aut | |
700 | 1 | |a Rochford, Rosemary |4 aut | |
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10.1186/1475-2875-7-238 doi (DE-627)SPR028603915 (SPR)1475-2875-7-238-e DE-627 ger DE-627 rakwb eng Asito, Amolo S verfasserin aut Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. Malaria (dpeaa)DE-He213 Peripheral Blood Mononuclear Cell (dpeaa)DE-He213 Cell Subset (dpeaa)DE-He213 Falciparum Malaria (dpeaa)DE-He213 Burkitt Lymphoma (dpeaa)DE-He213 Moormann, Ann M aut Kiprotich, Chelimo aut Ng'ang'a, Zipporah W aut Ploutz-Snyder, Robert aut Rochford, Rosemary aut Enthalten in Malaria journal London : BioMed Central, 2002 7(2008), 1 vom: 18. Nov. (DE-627)355986582 (DE-600)2091229-8 1475-2875 nnns volume:7 year:2008 number:1 day:18 month:11 https://dx.doi.org/10.1186/1475-2875-7-238 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 7 2008 1 18 11 |
spelling |
10.1186/1475-2875-7-238 doi (DE-627)SPR028603915 (SPR)1475-2875-7-238-e DE-627 ger DE-627 rakwb eng Asito, Amolo S verfasserin aut Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. Malaria (dpeaa)DE-He213 Peripheral Blood Mononuclear Cell (dpeaa)DE-He213 Cell Subset (dpeaa)DE-He213 Falciparum Malaria (dpeaa)DE-He213 Burkitt Lymphoma (dpeaa)DE-He213 Moormann, Ann M aut Kiprotich, Chelimo aut Ng'ang'a, Zipporah W aut Ploutz-Snyder, Robert aut Rochford, Rosemary aut Enthalten in Malaria journal London : BioMed Central, 2002 7(2008), 1 vom: 18. Nov. (DE-627)355986582 (DE-600)2091229-8 1475-2875 nnns volume:7 year:2008 number:1 day:18 month:11 https://dx.doi.org/10.1186/1475-2875-7-238 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 7 2008 1 18 11 |
allfields_unstemmed |
10.1186/1475-2875-7-238 doi (DE-627)SPR028603915 (SPR)1475-2875-7-238-e DE-627 ger DE-627 rakwb eng Asito, Amolo S verfasserin aut Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. Malaria (dpeaa)DE-He213 Peripheral Blood Mononuclear Cell (dpeaa)DE-He213 Cell Subset (dpeaa)DE-He213 Falciparum Malaria (dpeaa)DE-He213 Burkitt Lymphoma (dpeaa)DE-He213 Moormann, Ann M aut Kiprotich, Chelimo aut Ng'ang'a, Zipporah W aut Ploutz-Snyder, Robert aut Rochford, Rosemary aut Enthalten in Malaria journal London : BioMed Central, 2002 7(2008), 1 vom: 18. Nov. (DE-627)355986582 (DE-600)2091229-8 1475-2875 nnns volume:7 year:2008 number:1 day:18 month:11 https://dx.doi.org/10.1186/1475-2875-7-238 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 7 2008 1 18 11 |
allfieldsGer |
10.1186/1475-2875-7-238 doi (DE-627)SPR028603915 (SPR)1475-2875-7-238-e DE-627 ger DE-627 rakwb eng Asito, Amolo S verfasserin aut Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. Malaria (dpeaa)DE-He213 Peripheral Blood Mononuclear Cell (dpeaa)DE-He213 Cell Subset (dpeaa)DE-He213 Falciparum Malaria (dpeaa)DE-He213 Burkitt Lymphoma (dpeaa)DE-He213 Moormann, Ann M aut Kiprotich, Chelimo aut Ng'ang'a, Zipporah W aut Ploutz-Snyder, Robert aut Rochford, Rosemary aut Enthalten in Malaria journal London : BioMed Central, 2002 7(2008), 1 vom: 18. Nov. (DE-627)355986582 (DE-600)2091229-8 1475-2875 nnns volume:7 year:2008 number:1 day:18 month:11 https://dx.doi.org/10.1186/1475-2875-7-238 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 7 2008 1 18 11 |
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10.1186/1475-2875-7-238 doi (DE-627)SPR028603915 (SPR)1475-2875-7-238-e DE-627 ger DE-627 rakwb eng Asito, Amolo S verfasserin aut Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. Malaria (dpeaa)DE-He213 Peripheral Blood Mononuclear Cell (dpeaa)DE-He213 Cell Subset (dpeaa)DE-He213 Falciparum Malaria (dpeaa)DE-He213 Burkitt Lymphoma (dpeaa)DE-He213 Moormann, Ann M aut Kiprotich, Chelimo aut Ng'ang'a, Zipporah W aut Ploutz-Snyder, Robert aut Rochford, Rosemary aut Enthalten in Malaria journal London : BioMed Central, 2002 7(2008), 1 vom: 18. Nov. (DE-627)355986582 (DE-600)2091229-8 1475-2875 nnns volume:7 year:2008 number:1 day:18 month:11 https://dx.doi.org/10.1186/1475-2875-7-238 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 7 2008 1 18 11 |
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Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children |
abstract |
Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
abstractGer |
Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
abstract_unstemmed |
Background The effects of Plasmodium falciparum on B-cell homeostasis have not been well characterized. This study investigated whether an episode of acute malaria in young children results in changes in the peripheral B cell phenotype. Methods Using flow-cytofluorimetric analysis, the B cell phenotypes found in the peripheral blood of children aged 2–5 years were characterized during an episode of acute uncomplicated clinical malaria and four weeks post-recovery and in healthy age-matched controls. Results There was a significant decrease in $ CD19^{+} $ B lymphocytes during acute malaria. Characterization of the $ CD19^{+} $ B cell subsets in the peripheral blood based on expression of IgD and CD38 revealed a significant decrease in the numbers of naive 1 $ CD38^{-} %$ IgD^{+} $ B cells while there was an increase in $ CD38^{+} %$ IgD^{-} $ memory 3 B cells during acute malaria. Further analysis of the peripheral B cell phenotype also identified an expansion of transitional $ CD10^{+} %$ CD19^{+} $ B cells in children following an episode of acute malaria with up to 25% of total $ CD19^{+} $ B cell pool residing in this subset. Conclusion Children experiencing an episode of acute uncomplicated clinical malaria experienced profound disturbances in B cell homeostasis. © Asito et al; licensee BioMed Central Ltd. 2008. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
collection_details |
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title_short |
Alterations on peripheral B cell subsets following an acute uncomplicated clinical malaria infection in children |
url |
https://dx.doi.org/10.1186/1475-2875-7-238 |
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author2 |
Moormann, Ann M Kiprotich, Chelimo Ng'ang'a, Zipporah W Ploutz-Snyder, Robert Rochford, Rosemary |
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Moormann, Ann M Kiprotich, Chelimo Ng'ang'a, Zipporah W Ploutz-Snyder, Robert Rochford, Rosemary |
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doi_str |
10.1186/1475-2875-7-238 |
up_date |
2024-07-03T20:30:28.110Z |
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