Tamar A Smith-Norowitz, Sarah Shidid, Haram Abdelmajid, Nutchaya Amornruk, Wefag Ahmed, Yitzchok M Norowitz, Yecheskel Gold, Stephan Kohlhoff
{"title":"哮喘与非哮喘成人肺炎衣原体特异性T效应记忆淋巴细胞的比较。","authors":"Tamar A Smith-Norowitz, Sarah Shidid, Haram Abdelmajid, Nutchaya Amornruk, Wefag Ahmed, Yitzchok M Norowitz, Yecheskel Gold, Stephan Kohlhoff","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong><i>Chlamydia pneumoniae</i> is a gram-negative intracellular bacterium that causes respiratory infections, and may contribute to inflammation in asthma. Studies in our laboratory demonstrated that T lymphocyte/cytokine responses to <i>C. pneumoniae</i> in children with asthma were significantly higher, compared with non-asthma, which may indicate the presence of T effector memory (TEM) lymphocytes. In the present study, <i>C. pneumoniae</i> -specific TEMs and their intracellular cytokines were compared in asthmatic and non-asthmatic adults.</p><p><strong>Methods: </strong>Peripheral blood mononuclear cells (PBMC) (1×10<sup>6</sup>/mL) from asthmatic (N=6) and non-asthmatic (N=14) adults were infected for 24hr +/- <i>C. pneumoniae</i> TW-183 at a multiplicity of infection (MOI)=0.1 and cultured (48 hrs). Distributions of lymphocytes (CD3+, CD4+, CD8+) and TEM cells (CD4+CCR7-CD45RA+CD154+, CD8+CCR7-CD45RA+CD154+) were determined. Levels of intracellular Interleukin (IL)-2, IL-4, and Interferon (IFN)-gamma were measured (flow microfluorimetry).</p><p><strong>Results: </strong>Numbers of <i>C. pneumoniae</i>-stimulated CD3+CD4+CD45RO+CCR7-TEM (unstimulated, 1:10, 1:100) were higher in asthma compared with non-asthma (mean differences: unstimulated-stimulated) (-21±15, -17±15, -19±15; <i>P</i>=0.02, 0.04, 0.03, respectively) (Wilcoxon-signed rank test). However, CD3+CD4+IFN-gamma+TEMS (1:10, 1:100) were lower in asthma compared with non-asthma (mean differences: 2.2±5, 0.9±1; <i>P</i>=0.03, 0.04, respectively). When stratified according to <i>C. pneumoniae</i> IgG status, numbers of CD3+CD4+IL-2 (1:10) and CD3+CD4+IL-4+ (1:100) cells were higher in <i>C. pneumoniae</i> IgG+ compared with IgG- (mean differences: -0.2±0.2, -1.2±2.4; <i>P</i>=0.02. 0.05, respectively).</p><p><strong>Conclusion: </strong>Increased numbers of <i>C. pneumoniae</i> -stimulated TEM cells in asthma may indicate decreased effectiveness in clearing infection, suggesting an impaired IFN-gamma response.</p>","PeriodicalId":8228,"journal":{"name":"Annals of clinical and laboratory science","volume":"55 4","pages":"506-520"},"PeriodicalIF":1.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparison of <i>Chlamydia pneumoniae</i>-specific T Effector Memory Lymphocytes in Asthmatic and Non-Asthmatic Adults.\",\"authors\":\"Tamar A Smith-Norowitz, Sarah Shidid, Haram Abdelmajid, Nutchaya Amornruk, Wefag Ahmed, Yitzchok M Norowitz, Yecheskel Gold, Stephan Kohlhoff\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong><i>Chlamydia pneumoniae</i> is a gram-negative intracellular bacterium that causes respiratory infections, and may contribute to inflammation in asthma. Studies in our laboratory demonstrated that T lymphocyte/cytokine responses to <i>C. pneumoniae</i> in children with asthma were significantly higher, compared with non-asthma, which may indicate the presence of T effector memory (TEM) lymphocytes. In the present study, <i>C. pneumoniae</i> -specific TEMs and their intracellular cytokines were compared in asthmatic and non-asthmatic adults.</p><p><strong>Methods: </strong>Peripheral blood mononuclear cells (PBMC) (1×10<sup>6</sup>/mL) from asthmatic (N=6) and non-asthmatic (N=14) adults were infected for 24hr +/- <i>C. pneumoniae</i> TW-183 at a multiplicity of infection (MOI)=0.1 and cultured (48 hrs). Distributions of lymphocytes (CD3+, CD4+, CD8+) and TEM cells (CD4+CCR7-CD45RA+CD154+, CD8+CCR7-CD45RA+CD154+) were determined. Levels of intracellular Interleukin (IL)-2, IL-4, and Interferon (IFN)-gamma were measured (flow microfluorimetry).</p><p><strong>Results: </strong>Numbers of <i>C. pneumoniae</i>-stimulated CD3+CD4+CD45RO+CCR7-TEM (unstimulated, 1:10, 1:100) were higher in asthma compared with non-asthma (mean differences: unstimulated-stimulated) (-21±15, -17±15, -19±15; <i>P</i>=0.02, 0.04, 0.03, respectively) (Wilcoxon-signed rank test). However, CD3+CD4+IFN-gamma+TEMS (1:10, 1:100) were lower in asthma compared with non-asthma (mean differences: 2.2±5, 0.9±1; <i>P</i>=0.03, 0.04, respectively). When stratified according to <i>C. pneumoniae</i> IgG status, numbers of CD3+CD4+IL-2 (1:10) and CD3+CD4+IL-4+ (1:100) cells were higher in <i>C. pneumoniae</i> IgG+ compared with IgG- (mean differences: -0.2±0.2, -1.2±2.4; <i>P</i>=0.02. 0.05, respectively).</p><p><strong>Conclusion: </strong>Increased numbers of <i>C. pneumoniae</i> -stimulated TEM cells in asthma may indicate decreased effectiveness in clearing infection, suggesting an impaired IFN-gamma response.</p>\",\"PeriodicalId\":8228,\"journal\":{\"name\":\"Annals of clinical and laboratory science\",\"volume\":\"55 4\",\"pages\":\"506-520\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of clinical and laboratory science\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of clinical and laboratory science","FirstCategoryId":"3","ListUrlMain":"","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
Comparison of Chlamydia pneumoniae-specific T Effector Memory Lymphocytes in Asthmatic and Non-Asthmatic Adults.
Objective: Chlamydia pneumoniae is a gram-negative intracellular bacterium that causes respiratory infections, and may contribute to inflammation in asthma. Studies in our laboratory demonstrated that T lymphocyte/cytokine responses to C. pneumoniae in children with asthma were significantly higher, compared with non-asthma, which may indicate the presence of T effector memory (TEM) lymphocytes. In the present study, C. pneumoniae -specific TEMs and their intracellular cytokines were compared in asthmatic and non-asthmatic adults.
Methods: Peripheral blood mononuclear cells (PBMC) (1×106/mL) from asthmatic (N=6) and non-asthmatic (N=14) adults were infected for 24hr +/- C. pneumoniae TW-183 at a multiplicity of infection (MOI)=0.1 and cultured (48 hrs). Distributions of lymphocytes (CD3+, CD4+, CD8+) and TEM cells (CD4+CCR7-CD45RA+CD154+, CD8+CCR7-CD45RA+CD154+) were determined. Levels of intracellular Interleukin (IL)-2, IL-4, and Interferon (IFN)-gamma were measured (flow microfluorimetry).
Results: Numbers of C. pneumoniae-stimulated CD3+CD4+CD45RO+CCR7-TEM (unstimulated, 1:10, 1:100) were higher in asthma compared with non-asthma (mean differences: unstimulated-stimulated) (-21±15, -17±15, -19±15; P=0.02, 0.04, 0.03, respectively) (Wilcoxon-signed rank test). However, CD3+CD4+IFN-gamma+TEMS (1:10, 1:100) were lower in asthma compared with non-asthma (mean differences: 2.2±5, 0.9±1; P=0.03, 0.04, respectively). When stratified according to C. pneumoniae IgG status, numbers of CD3+CD4+IL-2 (1:10) and CD3+CD4+IL-4+ (1:100) cells were higher in C. pneumoniae IgG+ compared with IgG- (mean differences: -0.2±0.2, -1.2±2.4; P=0.02. 0.05, respectively).
Conclusion: Increased numbers of C. pneumoniae -stimulated TEM cells in asthma may indicate decreased effectiveness in clearing infection, suggesting an impaired IFN-gamma response.
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