Investigation of T lymphocyte subsets in children with Mycoplasma pneumoniae pneumonia
This study aims to characterize the majority of immune cell subsets in peripheral blood mononuclear cells in children with Mycoplasma pneumoniae pneumonia (MPP) by a 21-color flow cytometry panel. Patients who met the predetermined eligibility criteria for pneumonia diagnosis were recruited for the...
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description | This study aims to characterize the majority of immune cell subsets in peripheral blood mononuclear cells in children with
Mycoplasma pneumoniae
pneumonia (MPP) by a 21-color flow cytometry panel. Patients who met the predetermined eligibility criteria for pneumonia diagnosis were recruited for the research study. Multi-color flow cytometry was conducted on the peripheral blood mononuclear cells of each patient group, which were then subjected to dimensionality reduction and cluster analysis. In our study, the proportion of activated CD4 + T cell and naïve CD8 + T in children with MPP was higher than that of children with non-MPP, and the proportion of CD8 + T cell and central memory CD8 + T cell in MPP children was lower. Central memory CD4 + T cell and activated CD4 + T cell in the severe MPP were higher than those in the mild MPP. The highest proportions of CD8 + T cell, CD8 + Tn cell, activated CD8 + T cell, and total activated T cell were observed in the pulmonary consolidation-mucous group when compared to the pulmonary consolidation-necrosis and bronchiolitis groups. In the pulmonary consolidation-necrosis group, the proportions of central memory CD4 + T cell and T helper 17 cell were higher than those in pulmonary consolidation-mucous and bronchiolitis groups. In the bronchiolitis group, the percentages of CD4 + T cell, naïve CD4 + T cell, and T helper 2 cell were higher than those in pulmonary consolidation-mucous and the pulmonary consolidation-necrosis groups. The T lymphocyte subsets were different among various groups, offering new insights into the immune system of pediatric patients with
Mycoplasma pneumoniae
pneumonia. |
doi_str_mv | 10.1007/s12026-024-09576-4 |
format | Article |
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Mycoplasma pneumoniae
pneumonia (MPP) by a 21-color flow cytometry panel. Patients who met the predetermined eligibility criteria for pneumonia diagnosis were recruited for the research study. Multi-color flow cytometry was conducted on the peripheral blood mononuclear cells of each patient group, which were then subjected to dimensionality reduction and cluster analysis. In our study, the proportion of activated CD4 + T cell and naïve CD8 + T in children with MPP was higher than that of children with non-MPP, and the proportion of CD8 + T cell and central memory CD8 + T cell in MPP children was lower. Central memory CD4 + T cell and activated CD4 + T cell in the severe MPP were higher than those in the mild MPP. The highest proportions of CD8 + T cell, CD8 + Tn cell, activated CD8 + T cell, and total activated T cell were observed in the pulmonary consolidation-mucous group when compared to the pulmonary consolidation-necrosis and bronchiolitis groups. In the pulmonary consolidation-necrosis group, the proportions of central memory CD4 + T cell and T helper 17 cell were higher than those in pulmonary consolidation-mucous and bronchiolitis groups. In the bronchiolitis group, the percentages of CD4 + T cell, naïve CD4 + T cell, and T helper 2 cell were higher than those in pulmonary consolidation-mucous and the pulmonary consolidation-necrosis groups. The T lymphocyte subsets were different among various groups, offering new insights into the immune system of pediatric patients with
Mycoplasma pneumoniae
pneumonia.</description><identifier>ISSN: 0257-277X</identifier><identifier>ISSN: 1559-0755</identifier><identifier>EISSN: 1559-0755</identifier><identifier>DOI: 10.1007/s12026-024-09576-4</identifier><identifier>PMID: 39714538</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adolescent ; Allergology ; Biomedical and Life Sciences ; Biomedicine ; Bronchopneumonia ; CD4 antigen ; CD4-Positive T-Lymphocytes - immunology ; CD8 antigen ; CD8-Positive T-Lymphocytes - immunology ; Child ; Child, Preschool ; Children ; Female ; Flow Cytometry ; Humans ; Immune system ; Immunologic Memory ; Immunological memory ; Immunology ; Immunophenotyping ; Internal Medicine ; Leukocytes (mononuclear) ; Lymphocyte Activation ; Lymphocytes ; Lymphocytes T ; Male ; Medicine/Public Health ; Memory cells ; Mycoplasma pneumoniae ; Mycoplasma pneumoniae - immunology ; Necrosis ; Pediatrics ; Peripheral blood mononuclear cells ; Pneumonia ; Pneumonia, Mycoplasma - diagnosis ; Pneumonia, Mycoplasma - immunology ; T-Lymphocyte Subsets - immunology</subject><ispartof>Immunologic research, 2024-12, Vol.73 (1), p.24</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024 Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>Copyright Springer Nature B.V. Dec 2025</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12026-024-09576-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12026-024-09576-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39714538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Deze</creatorcontrib><creatorcontrib>Zheng, Huiwen</creatorcontrib><creatorcontrib>Wang, Xiaotong</creatorcontrib><creatorcontrib>Li, Feina</creatorcontrib><creatorcontrib>Wang, Heng</creatorcontrib><creatorcontrib>Chen, Hao</creatorcontrib><creatorcontrib>Shen, Chen</creatorcontrib><creatorcontrib>Zhao, Shunying</creatorcontrib><title>Investigation of T lymphocyte subsets in children with Mycoplasma pneumoniae pneumonia</title><title>Immunologic research</title><addtitle>Immunol Res</addtitle><addtitle>Immunol Res</addtitle><description>This study aims to characterize the majority of immune cell subsets in peripheral blood mononuclear cells in children with
Mycoplasma pneumoniae
pneumonia (MPP) by a 21-color flow cytometry panel. Patients who met the predetermined eligibility criteria for pneumonia diagnosis were recruited for the research study. Multi-color flow cytometry was conducted on the peripheral blood mononuclear cells of each patient group, which were then subjected to dimensionality reduction and cluster analysis. In our study, the proportion of activated CD4 + T cell and naïve CD8 + T in children with MPP was higher than that of children with non-MPP, and the proportion of CD8 + T cell and central memory CD8 + T cell in MPP children was lower. Central memory CD4 + T cell and activated CD4 + T cell in the severe MPP were higher than those in the mild MPP. The highest proportions of CD8 + T cell, CD8 + Tn cell, activated CD8 + T cell, and total activated T cell were observed in the pulmonary consolidation-mucous group when compared to the pulmonary consolidation-necrosis and bronchiolitis groups. In the pulmonary consolidation-necrosis group, the proportions of central memory CD4 + T cell and T helper 17 cell were higher than those in pulmonary consolidation-mucous and bronchiolitis groups. In the bronchiolitis group, the percentages of CD4 + T cell, naïve CD4 + T cell, and T helper 2 cell were higher than those in pulmonary consolidation-mucous and the pulmonary consolidation-necrosis groups. The T lymphocyte subsets were different among various groups, offering new insights into the immune system of pediatric patients with
Mycoplasma pneumoniae
pneumonia.</description><subject>Adolescent</subject><subject>Allergology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bronchopneumonia</subject><subject>CD4 antigen</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunologic Memory</subject><subject>Immunological memory</subject><subject>Immunology</subject><subject>Immunophenotyping</subject><subject>Internal Medicine</subject><subject>Leukocytes (mononuclear)</subject><subject>Lymphocyte Activation</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medicine/Public Health</subject><subject>Memory cells</subject><subject>Mycoplasma pneumoniae</subject><subject>Mycoplasma pneumoniae - immunology</subject><subject>Necrosis</subject><subject>Pediatrics</subject><subject>Peripheral blood mononuclear cells</subject><subject>Pneumonia</subject><subject>Pneumonia, Mycoplasma - diagnosis</subject><subject>Pneumonia, Mycoplasma - immunology</subject><subject>T-Lymphocyte Subsets - immunology</subject><issn>0257-277X</issn><issn>1559-0755</issn><issn>1559-0755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1Lw0AQhhdRtFb_gAdZ8OIlOvuV3Ryl-FFQvFTxtmyTiY0km5hNlPx7Y1speJqBeXiZmYeQMwZXDEBfB8aBxxFwGUGidBzJPTJhSiURaKX2yQS40hHX-u2IHIfwAcBiKcUhORKJZlIJMyGvc_-FoSveXVfUntY5XdByqJpVnQ4d0tAvA3aBFp6mq6LMWvT0u-hW9GlI66Z0oXK08dhXtS8c7toTcpC7MuDptk7Jy93tYvYQPT7fz2c3j1HDuJGR1pjGnDuTgUKXQ4YYC85gCblSmTOCO8hSmcTSmFzjyGRSok4yx9ElTIopudzkNm392Y-H2KoIKZal81j3wQomjQLGmBnRi3_oR923ftxuTcUm5gAjdb6l-mWFmW3aonLtYP8-NgJiA4Rx5N-x3cUwsL9e7MaLHb3YtRcrxQ_8OH5e</recordid><startdate>20241223</startdate><enddate>20241223</enddate><creator>Li, Deze</creator><creator>Zheng, Huiwen</creator><creator>Wang, Xiaotong</creator><creator>Li, Feina</creator><creator>Wang, Heng</creator><creator>Chen, Hao</creator><creator>Shen, Chen</creator><creator>Zhao, Shunying</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>20241223</creationdate><title>Investigation of T lymphocyte subsets in children with Mycoplasma pneumoniae pneumonia</title><author>Li, Deze ; Zheng, Huiwen ; Wang, Xiaotong ; Li, Feina ; Wang, Heng ; Chen, Hao ; Shen, Chen ; Zhao, Shunying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1284-77ec622a8d05eaf0dee63210b0f55da832a0dc496488f7e5ead44e79da2ea9143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Allergology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bronchopneumonia</topic><topic>CD4 antigen</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8 antigen</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunologic Memory</topic><topic>Immunological memory</topic><topic>Immunology</topic><topic>Immunophenotyping</topic><topic>Internal Medicine</topic><topic>Leukocytes (mononuclear)</topic><topic>Lymphocyte Activation</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medicine/Public Health</topic><topic>Memory cells</topic><topic>Mycoplasma pneumoniae</topic><topic>Mycoplasma pneumoniae - immunology</topic><topic>Necrosis</topic><topic>Pediatrics</topic><topic>Peripheral blood mononuclear cells</topic><topic>Pneumonia</topic><topic>Pneumonia, Mycoplasma - diagnosis</topic><topic>Pneumonia, Mycoplasma - immunology</topic><topic>T-Lymphocyte Subsets - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Deze</creatorcontrib><creatorcontrib>Zheng, Huiwen</creatorcontrib><creatorcontrib>Wang, Xiaotong</creatorcontrib><creatorcontrib>Li, Feina</creatorcontrib><creatorcontrib>Wang, Heng</creatorcontrib><creatorcontrib>Chen, Hao</creatorcontrib><creatorcontrib>Shen, Chen</creatorcontrib><creatorcontrib>Zhao, Shunying</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Immunologic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Deze</au><au>Zheng, Huiwen</au><au>Wang, Xiaotong</au><au>Li, Feina</au><au>Wang, Heng</au><au>Chen, Hao</au><au>Shen, Chen</au><au>Zhao, Shunying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of T lymphocyte subsets in children with Mycoplasma pneumoniae pneumonia</atitle><jtitle>Immunologic research</jtitle><stitle>Immunol Res</stitle><addtitle>Immunol Res</addtitle><date>2024-12-23</date><risdate>2024</risdate><volume>73</volume><issue>1</issue><spage>24</spage><pages>24-</pages><issn>0257-277X</issn><issn>1559-0755</issn><eissn>1559-0755</eissn><abstract>This study aims to characterize the majority of immune cell subsets in peripheral blood mononuclear cells in children with
Mycoplasma pneumoniae
pneumonia (MPP) by a 21-color flow cytometry panel. Patients who met the predetermined eligibility criteria for pneumonia diagnosis were recruited for the research study. Multi-color flow cytometry was conducted on the peripheral blood mononuclear cells of each patient group, which were then subjected to dimensionality reduction and cluster analysis. In our study, the proportion of activated CD4 + T cell and naïve CD8 + T in children with MPP was higher than that of children with non-MPP, and the proportion of CD8 + T cell and central memory CD8 + T cell in MPP children was lower. Central memory CD4 + T cell and activated CD4 + T cell in the severe MPP were higher than those in the mild MPP. The highest proportions of CD8 + T cell, CD8 + Tn cell, activated CD8 + T cell, and total activated T cell were observed in the pulmonary consolidation-mucous group when compared to the pulmonary consolidation-necrosis and bronchiolitis groups. In the pulmonary consolidation-necrosis group, the proportions of central memory CD4 + T cell and T helper 17 cell were higher than those in pulmonary consolidation-mucous and bronchiolitis groups. In the bronchiolitis group, the percentages of CD4 + T cell, naïve CD4 + T cell, and T helper 2 cell were higher than those in pulmonary consolidation-mucous and the pulmonary consolidation-necrosis groups. The T lymphocyte subsets were different among various groups, offering new insights into the immune system of pediatric patients with
Mycoplasma pneumoniae
pneumonia.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>39714538</pmid><doi>10.1007/s12026-024-09576-4</doi></addata></record> |
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subjects | Adolescent Allergology Biomedical and Life Sciences Biomedicine Bronchopneumonia CD4 antigen CD4-Positive T-Lymphocytes - immunology CD8 antigen CD8-Positive T-Lymphocytes - immunology Child Child, Preschool Children Female Flow Cytometry Humans Immune system Immunologic Memory Immunological memory Immunology Immunophenotyping Internal Medicine Leukocytes (mononuclear) Lymphocyte Activation Lymphocytes Lymphocytes T Male Medicine/Public Health Memory cells Mycoplasma pneumoniae Mycoplasma pneumoniae - immunology Necrosis Pediatrics Peripheral blood mononuclear cells Pneumonia Pneumonia, Mycoplasma - diagnosis Pneumonia, Mycoplasma - immunology T-Lymphocyte Subsets - immunology |
title | Investigation of T lymphocyte subsets in children with Mycoplasma pneumoniae pneumonia |
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