IMMUNE BIOMARKERS IN RELATION TO EXPOSURE TO PARTICULATE MATTER: A Cross-Sectional Survey in 17 Cities of Central Europe
Human population data on air pollution and its effects on the immune system are scarce. A survey was conducted within the framework of the Central European Study of Air Quality and Respiratory Health (CESAR) to measure a panel of immune biomarkers in children of Bulgaria, Czech Republic, Hungary, Po...
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creator | Leonardi, G. S. Houthuijs, D. Steerenberg, P. A. Fletcher, T. Armstrong, B. Antova, T. Lochman, I. Lochmanová, A. Rudnai, P. Erdei, E. Musial, J. Jazwiec-Kanyion, B. Niciu, E. M. Durbaca, S. Fabiánová, E. Koppová, K. Lebret, E. Brunekreef, B. Van Loveren, H. |
description | Human population data on air pollution and its effects on the immune system are scarce. A survey was conducted within the framework of the Central European Study of Air Quality and Respiratory Health (CESAR) to measure a panel of immune biomarkers in children of Bulgaria, Czech Republic, Hungary, Poland, Romania, and Slovakia. Seventeen cities were chosen to represent a wide range of exposure to outdoor air pollution. In each, ambient particulate matter of less than 10 μm diameter and less than 2.5 μm diameter (PM10 and PM2.5) were measured with a Harvard impactor. Blood was collected from 366 school children aged 9 to 11 yr between 11 April and 10 May 1996. The percentage of B, total T, CD4 +, CD8 +, and natural killer (NK) lymphocytes was determined by flow cytometry (Becton Dickinson); total immunoglobulins of class G, M, A and E (IgG, IgM, IgA, and IgE) were measured in serum using nephelometry (Behring). Associations between PM and each log-transformed biomarker concentration were studied by linear regression, in a two-stage model. The yearly average concentrations varied from 41 to 96 μg/m3 for PM10 across the 17 study areas, from 29 to 67 μg/m3 for PM2.5, and from 12 to 38 μg/m3 for PM10-2.5 (coarse). Number of B, CD4 +, CD8 +, and NK lymphocytes increased with increasing concentration of PM, having adjusted for age, gender, parental smoking, laboratory of analysis, and recent respiratory illness. Differences in lymphocyte number were larger and statistically significant for exposure to PM2.5. Similar results were found when we examined the association between PM and lymphocyte number separately for each laboratory. Total IgG was increased with increasing concentration of PM, significantly in the case of PM2.5. When we repeated the analyses with two other statistical approaches the results did not differ from those reported here. The effect of coarse PM on lymphocyte numbers appears small in comparison to PM2.5. One possible interpretation of our findings is that long-term exposure to airborne particulates leads to inflammation of the airways and activation of the cellular and humoral immune system. |
doi_str_mv | 10.1080/08958370050164833 |
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S. ; Houthuijs, D. ; Steerenberg, P. A. ; Fletcher, T. ; Armstrong, B. ; Antova, T. ; Lochman, I. ; Lochmanová, A. ; Rudnai, P. ; Erdei, E. ; Musial, J. ; Jazwiec-Kanyion, B. ; Niciu, E. M. ; Durbaca, S. ; Fabiánová, E. ; Koppová, K. ; Lebret, E. ; Brunekreef, B. ; Van Loveren, H.</creator><creatorcontrib>Leonardi, G. S. ; Houthuijs, D. ; Steerenberg, P. A. ; Fletcher, T. ; Armstrong, B. ; Antova, T. ; Lochman, I. ; Lochmanová, A. ; Rudnai, P. ; Erdei, E. ; Musial, J. ; Jazwiec-Kanyion, B. ; Niciu, E. M. ; Durbaca, S. ; Fabiánová, E. ; Koppová, K. ; Lebret, E. ; Brunekreef, B. ; Van Loveren, H.</creatorcontrib><description>Human population data on air pollution and its effects on the immune system are scarce. A survey was conducted within the framework of the Central European Study of Air Quality and Respiratory Health (CESAR) to measure a panel of immune biomarkers in children of Bulgaria, Czech Republic, Hungary, Poland, Romania, and Slovakia. Seventeen cities were chosen to represent a wide range of exposure to outdoor air pollution. In each, ambient particulate matter of less than 10 μm diameter and less than 2.5 μm diameter (PM10 and PM2.5) were measured with a Harvard impactor. Blood was collected from 366 school children aged 9 to 11 yr between 11 April and 10 May 1996. The percentage of B, total T, CD4 +, CD8 +, and natural killer (NK) lymphocytes was determined by flow cytometry (Becton Dickinson); total immunoglobulins of class G, M, A and E (IgG, IgM, IgA, and IgE) were measured in serum using nephelometry (Behring). Associations between PM and each log-transformed biomarker concentration were studied by linear regression, in a two-stage model. The yearly average concentrations varied from 41 to 96 μg/m3 for PM10 across the 17 study areas, from 29 to 67 μg/m3 for PM2.5, and from 12 to 38 μg/m3 for PM10-2.5 (coarse). Number of B, CD4 +, CD8 +, and NK lymphocytes increased with increasing concentration of PM, having adjusted for age, gender, parental smoking, laboratory of analysis, and recent respiratory illness. Differences in lymphocyte number were larger and statistically significant for exposure to PM2.5. Similar results were found when we examined the association between PM and lymphocyte number separately for each laboratory. Total IgG was increased with increasing concentration of PM, significantly in the case of PM2.5. When we repeated the analyses with two other statistical approaches the results did not differ from those reported here. The effect of coarse PM on lymphocyte numbers appears small in comparison to PM2.5. One possible interpretation of our findings is that long-term exposure to airborne particulates leads to inflammation of the airways and activation of the cellular and humoral immune system.</description><identifier>ISSN: 0895-8378</identifier><identifier>EISSN: 1091-7691</identifier><identifier>DOI: 10.1080/08958370050164833</identifier><identifier>PMID: 12881884</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Air Pollutants - immunology ; Air Pollution - adverse effects ; Biomarkers - blood ; Child ; Cities ; Cross-Sectional Studies ; Environmental Exposure ; Europe - epidemiology ; Female ; Humans ; Immunoglobulins - immunology ; Lymphocyte Count ; Lymphocytes - cytology ; Lymphocytes - immunology ; Male ; Neutrophils - immunology ; Respiratory Tract Diseases - epidemiology ; Respiratory Tract Diseases - immunology ; Seroepidemiologic Studies ; Urban Population</subject><ispartof>Inhalation toxicology, 2000, Vol.12 (S4), p.1-14</ispartof><rights>2000 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-2d166cc007d92ad945c27019c15e892ddf952d6408f9e481a78246fb6d22ee733</citedby><cites>FETCH-LOGICAL-c431t-2d166cc007d92ad945c27019c15e892ddf952d6408f9e481a78246fb6d22ee733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/08958370050164833$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/08958370050164833$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,780,784,4022,27922,27923,27924,59646,59752,60435,60541,61220,61255,61401,61436</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12881884$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leonardi, G. S.</creatorcontrib><creatorcontrib>Houthuijs, D.</creatorcontrib><creatorcontrib>Steerenberg, P. A.</creatorcontrib><creatorcontrib>Fletcher, T.</creatorcontrib><creatorcontrib>Armstrong, B.</creatorcontrib><creatorcontrib>Antova, T.</creatorcontrib><creatorcontrib>Lochman, I.</creatorcontrib><creatorcontrib>Lochmanová, A.</creatorcontrib><creatorcontrib>Rudnai, P.</creatorcontrib><creatorcontrib>Erdei, E.</creatorcontrib><creatorcontrib>Musial, J.</creatorcontrib><creatorcontrib>Jazwiec-Kanyion, B.</creatorcontrib><creatorcontrib>Niciu, E. M.</creatorcontrib><creatorcontrib>Durbaca, S.</creatorcontrib><creatorcontrib>Fabiánová, E.</creatorcontrib><creatorcontrib>Koppová, K.</creatorcontrib><creatorcontrib>Lebret, E.</creatorcontrib><creatorcontrib>Brunekreef, B.</creatorcontrib><creatorcontrib>Van Loveren, H.</creatorcontrib><title>IMMUNE BIOMARKERS IN RELATION TO EXPOSURE TO PARTICULATE MATTER: A Cross-Sectional Survey in 17 Cities of Central Europe</title><title>Inhalation toxicology</title><addtitle>Inhal Toxicol</addtitle><description>Human population data on air pollution and its effects on the immune system are scarce. A survey was conducted within the framework of the Central European Study of Air Quality and Respiratory Health (CESAR) to measure a panel of immune biomarkers in children of Bulgaria, Czech Republic, Hungary, Poland, Romania, and Slovakia. Seventeen cities were chosen to represent a wide range of exposure to outdoor air pollution. In each, ambient particulate matter of less than 10 μm diameter and less than 2.5 μm diameter (PM10 and PM2.5) were measured with a Harvard impactor. Blood was collected from 366 school children aged 9 to 11 yr between 11 April and 10 May 1996. The percentage of B, total T, CD4 +, CD8 +, and natural killer (NK) lymphocytes was determined by flow cytometry (Becton Dickinson); total immunoglobulins of class G, M, A and E (IgG, IgM, IgA, and IgE) were measured in serum using nephelometry (Behring). Associations between PM and each log-transformed biomarker concentration were studied by linear regression, in a two-stage model. The yearly average concentrations varied from 41 to 96 μg/m3 for PM10 across the 17 study areas, from 29 to 67 μg/m3 for PM2.5, and from 12 to 38 μg/m3 for PM10-2.5 (coarse). Number of B, CD4 +, CD8 +, and NK lymphocytes increased with increasing concentration of PM, having adjusted for age, gender, parental smoking, laboratory of analysis, and recent respiratory illness. Differences in lymphocyte number were larger and statistically significant for exposure to PM2.5. Similar results were found when we examined the association between PM and lymphocyte number separately for each laboratory. Total IgG was increased with increasing concentration of PM, significantly in the case of PM2.5. When we repeated the analyses with two other statistical approaches the results did not differ from those reported here. The effect of coarse PM on lymphocyte numbers appears small in comparison to PM2.5. One possible interpretation of our findings is that long-term exposure to airborne particulates leads to inflammation of the airways and activation of the cellular and humoral immune system.</description><subject>Air Pollutants - immunology</subject><subject>Air Pollution - adverse effects</subject><subject>Biomarkers - blood</subject><subject>Child</subject><subject>Cities</subject><subject>Cross-Sectional Studies</subject><subject>Environmental Exposure</subject><subject>Europe - epidemiology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoglobulins - immunology</subject><subject>Lymphocyte Count</subject><subject>Lymphocytes - cytology</subject><subject>Lymphocytes - immunology</subject><subject>Male</subject><subject>Neutrophils - immunology</subject><subject>Respiratory Tract Diseases - epidemiology</subject><subject>Respiratory Tract Diseases - immunology</subject><subject>Seroepidemiologic Studies</subject><subject>Urban Population</subject><issn>0895-8378</issn><issn>1091-7691</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF9v0zAUxS0EYmXwAXhBfuItzHb-2AZeQmRGtLaZ0lTizfJsR8uUxp2dAP32pGolhCbt6V7p_M7RvQeA9xh9woihK8R4ymKKUIpwlrA4fgEWGHEc0Yzjl2Bx1KMZYBfgTQgPCKEMxfQ1uMCEMcxYsgB_ytVquxbwW1mt8vpG1BtYrmEtlnlTVmvYVFD8vK0221oc99u8bspiO4sCrvKmEfVnmMPCuxCijdVj5wbVw83kf9kD7AaIKSy6sbMBuhYWdhj9LIvJu719C161qg_23Xlegu130RQ_omV1XRb5MtJJjMeIGJxlWiNEDSfK8CTVhCLMNU4t48SYlqfEZAliLbcJw4oykmTtXWYIsZbG8SX4eMrde_c42TDKXRe07Xs1WDcFiZM0JQklM4hPoD6-420r977bKX-QGMlj3fJJ3bPnwzl8uttZ889x7ncGvp6Abmid36nfzvdGjurQO996NeguyPi5_C__2e-t6sd7rbyVD27yc9nhmev-AmeCmXA</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Leonardi, G. 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A.</au><au>Fletcher, T.</au><au>Armstrong, B.</au><au>Antova, T.</au><au>Lochman, I.</au><au>Lochmanová, A.</au><au>Rudnai, P.</au><au>Erdei, E.</au><au>Musial, J.</au><au>Jazwiec-Kanyion, B.</au><au>Niciu, E. M.</au><au>Durbaca, S.</au><au>Fabiánová, E.</au><au>Koppová, K.</au><au>Lebret, E.</au><au>Brunekreef, B.</au><au>Van Loveren, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IMMUNE BIOMARKERS IN RELATION TO EXPOSURE TO PARTICULATE MATTER: A Cross-Sectional Survey in 17 Cities of Central Europe</atitle><jtitle>Inhalation toxicology</jtitle><addtitle>Inhal Toxicol</addtitle><date>2000</date><risdate>2000</risdate><volume>12</volume><issue>S4</issue><spage>1</spage><epage>14</epage><pages>1-14</pages><issn>0895-8378</issn><eissn>1091-7691</eissn><abstract>Human population data on air pollution and its effects on the immune system are scarce. A survey was conducted within the framework of the Central European Study of Air Quality and Respiratory Health (CESAR) to measure a panel of immune biomarkers in children of Bulgaria, Czech Republic, Hungary, Poland, Romania, and Slovakia. Seventeen cities were chosen to represent a wide range of exposure to outdoor air pollution. In each, ambient particulate matter of less than 10 μm diameter and less than 2.5 μm diameter (PM10 and PM2.5) were measured with a Harvard impactor. Blood was collected from 366 school children aged 9 to 11 yr between 11 April and 10 May 1996. The percentage of B, total T, CD4 +, CD8 +, and natural killer (NK) lymphocytes was determined by flow cytometry (Becton Dickinson); total immunoglobulins of class G, M, A and E (IgG, IgM, IgA, and IgE) were measured in serum using nephelometry (Behring). Associations between PM and each log-transformed biomarker concentration were studied by linear regression, in a two-stage model. The yearly average concentrations varied from 41 to 96 μg/m3 for PM10 across the 17 study areas, from 29 to 67 μg/m3 for PM2.5, and from 12 to 38 μg/m3 for PM10-2.5 (coarse). Number of B, CD4 +, CD8 +, and NK lymphocytes increased with increasing concentration of PM, having adjusted for age, gender, parental smoking, laboratory of analysis, and recent respiratory illness. Differences in lymphocyte number were larger and statistically significant for exposure to PM2.5. Similar results were found when we examined the association between PM and lymphocyte number separately for each laboratory. Total IgG was increased with increasing concentration of PM, significantly in the case of PM2.5. When we repeated the analyses with two other statistical approaches the results did not differ from those reported here. The effect of coarse PM on lymphocyte numbers appears small in comparison to PM2.5. One possible interpretation of our findings is that long-term exposure to airborne particulates leads to inflammation of the airways and activation of the cellular and humoral immune system.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>12881884</pmid><doi>10.1080/08958370050164833</doi><tpages>14</tpages></addata></record> |
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subjects | Air Pollutants - immunology Air Pollution - adverse effects Biomarkers - blood Child Cities Cross-Sectional Studies Environmental Exposure Europe - epidemiology Female Humans Immunoglobulins - immunology Lymphocyte Count Lymphocytes - cytology Lymphocytes - immunology Male Neutrophils - immunology Respiratory Tract Diseases - epidemiology Respiratory Tract Diseases - immunology Seroepidemiologic Studies Urban Population |
title | IMMUNE BIOMARKERS IN RELATION TO EXPOSURE TO PARTICULATE MATTER: A Cross-Sectional Survey in 17 Cities of Central Europe |
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