CD18 adhesion blockade decreases bacterial clearance and neutrophil recruitment after intrapulmonary E. coli, but not after S. aureus
Leukocyte emigration in the lung occurs by both CD18‐dependent and ‐independent mechanisms that are stimulus specific. We examined the effect of CD18 blockade (mAb 60.3) on neutrophil (PMN) emigration into, and bacterial clearance from, the lung. After intravenous treatment with either mAb 60.3 or s...
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Veröffentlicht in: | Journal of leukocyte biology 1997-02, Vol.61 (2), p.167-172 |
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creator | Ramamoorthy, Chandra Sasaki, Steve S. Su, Daniel L. Sharar, Sam R. Harlan, John M. Winn, Robert K. |
description | Leukocyte emigration in the lung occurs by both CD18‐dependent and ‐independent mechanisms that are stimulus specific. We examined the effect of CD18 blockade (mAb 60.3) on neutrophil (PMN) emigration into, and bacterial clearance from, the lung. After intravenous treatment with either mAb 60.3 or saline, rabbits were given an intralobar inoculation with 109 colony‐forming units of either Staphylococcus aureus or Escherichia coli. Four hours after inoculation, lungs were lavaged to assess PMN emigration. CD18 blockade reduced PMN emigration to E. coli by 76% but only 45% to S. aureus. Experiments to determine bacterial recovery from the lungs at 4, 8, and 24 h after inoculation showed that CD18 blockade impaired the early (4 h) clearance of E. coli but not S. aureus. These findings suggest that PMN emigration to intrapulmonary S. aureus is largely CD18‐independent. In contrast, intrapulmonary E. coli elicits CD18‐mediated PMN emigration. CD18 blockade results in impaired clearance of E. coli but not S. aureus from the lung. J. Leukoc. Biol. 61: 167–172; 1997. |
doi_str_mv | 10.1002/jlb.61.2.167 |
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We examined the effect of CD18 blockade (mAb 60.3) on neutrophil (PMN) emigration into, and bacterial clearance from, the lung. After intravenous treatment with either mAb 60.3 or saline, rabbits were given an intralobar inoculation with 109 colony‐forming units of either Staphylococcus aureus or Escherichia coli. Four hours after inoculation, lungs were lavaged to assess PMN emigration. CD18 blockade reduced PMN emigration to E. coli by 76% but only 45% to S. aureus. Experiments to determine bacterial recovery from the lungs at 4, 8, and 24 h after inoculation showed that CD18 blockade impaired the early (4 h) clearance of E. coli but not S. aureus. These findings suggest that PMN emigration to intrapulmonary S. aureus is largely CD18‐independent. In contrast, intrapulmonary E. coli elicits CD18‐mediated PMN emigration. CD18 blockade results in impaired clearance of E. coli but not S. aureus from the lung. J. Leukoc. Biol. 61: 167–172; 1997.</description><identifier>ISSN: 0741-5400</identifier><identifier>EISSN: 1938-3673</identifier><identifier>DOI: 10.1002/jlb.61.2.167</identifier><identifier>PMID: 9021922</identifier><language>eng</language><publisher>United States: Society for Leukocyte Biology</publisher><subject>alveolar macrophage ; Animals ; Antibodies, Monoclonal - pharmacology ; CD18 Antigens - immunology ; Cell Adhesion - immunology ; Cell Movement - immunology ; Escherichia coli ; Escherichia coli Infections - immunology ; Escherichia coli Infections - microbiology ; Leukocyte Count ; Lung - microbiology ; lung lavage ; Neutrophils - immunology ; Neutrophils - microbiology ; Rabbits ; Staphylococcal Infections - immunology ; Staphylococcal Infections - microbiology ; β2 integrins</subject><ispartof>Journal of leukocyte biology, 1997-02, Vol.61 (2), p.167-172</ispartof><rights>1997 Society for Leukocyte Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4277-e57018605ac3ec6dc9d26c8a0de3d90f7fe41a51b785be29ea435a5e23add4b43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjlb.61.2.167$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjlb.61.2.167$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9021922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramamoorthy, Chandra</creatorcontrib><creatorcontrib>Sasaki, Steve S.</creatorcontrib><creatorcontrib>Su, Daniel L.</creatorcontrib><creatorcontrib>Sharar, Sam R.</creatorcontrib><creatorcontrib>Harlan, John M.</creatorcontrib><creatorcontrib>Winn, Robert K.</creatorcontrib><title>CD18 adhesion blockade decreases bacterial clearance and neutrophil recruitment after intrapulmonary E. coli, but not after S. aureus</title><title>Journal of leukocyte biology</title><addtitle>J Leukoc Biol</addtitle><description>Leukocyte emigration in the lung occurs by both CD18‐dependent and ‐independent mechanisms that are stimulus specific. We examined the effect of CD18 blockade (mAb 60.3) on neutrophil (PMN) emigration into, and bacterial clearance from, the lung. After intravenous treatment with either mAb 60.3 or saline, rabbits were given an intralobar inoculation with 109 colony‐forming units of either Staphylococcus aureus or Escherichia coli. Four hours after inoculation, lungs were lavaged to assess PMN emigration. CD18 blockade reduced PMN emigration to E. coli by 76% but only 45% to S. aureus. Experiments to determine bacterial recovery from the lungs at 4, 8, and 24 h after inoculation showed that CD18 blockade impaired the early (4 h) clearance of E. coli but not S. aureus. These findings suggest that PMN emigration to intrapulmonary S. aureus is largely CD18‐independent. In contrast, intrapulmonary E. coli elicits CD18‐mediated PMN emigration. CD18 blockade results in impaired clearance of E. coli but not S. aureus from the lung. J. Leukoc. Biol. 61: 167–172; 1997.</description><subject>alveolar macrophage</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - pharmacology</subject><subject>CD18 Antigens - immunology</subject><subject>Cell Adhesion - immunology</subject><subject>Cell Movement - immunology</subject><subject>Escherichia coli</subject><subject>Escherichia coli Infections - immunology</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Leukocyte Count</subject><subject>Lung - microbiology</subject><subject>lung lavage</subject><subject>Neutrophils - immunology</subject><subject>Neutrophils - microbiology</subject><subject>Rabbits</subject><subject>Staphylococcal Infections - immunology</subject><subject>Staphylococcal Infections - microbiology</subject><subject>β2 integrins</subject><issn>0741-5400</issn><issn>1938-3673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS1EVbYLN65IvsCpSW0nsZMjXVpotRIH4GxN7Anr4iSLnSjqD-B_Y5SlRzjNYb55T_MeIa85yzlj4urBt7nkuci5VM_IhjdFnRVSFc_JhqmSZ1XJ2AtyEeMDY6wQkp2T84YJ3gixIb92H3hNwR4wunGgrR_ND7BILZqAEDHSFsyEwYGnxiMEGAxSGCwdcJ7CeDw4T0OCZzf1OEwUukRTN0wBjrPvxwHCI73JqRm9u6TtPNFh_Et9ySnMAef4kpx14CO-Os0t-XZ783X3Kdt__ni3e7_PTCmUyrBSjNeSVWAKNNKaxgppamAWC9uwTnVYcqh4q-qqRdEglEUFFYoCrC3bstiSd6vuMYw_Z4yT7l006D0MOM5Rq7pmZc3_D3KZsqxS1FtyuYImjDEG7PQxuD79rDnTf-rRqR4tuRbpRiX8zUl3bnu0T_Cpj7Tn635xHh__qaXv99ds1Xy73hzc98PiAurYg_fJQehlWZ68fwO7C6kv</recordid><startdate>199702</startdate><enddate>199702</enddate><creator>Ramamoorthy, Chandra</creator><creator>Sasaki, Steve S.</creator><creator>Su, Daniel L.</creator><creator>Sharar, Sam R.</creator><creator>Harlan, John M.</creator><creator>Winn, Robert K.</creator><general>Society for Leukocyte Biology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199702</creationdate><title>CD18 adhesion blockade decreases bacterial clearance and neutrophil recruitment after intrapulmonary E. coli, but not after S. aureus</title><author>Ramamoorthy, Chandra ; 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We examined the effect of CD18 blockade (mAb 60.3) on neutrophil (PMN) emigration into, and bacterial clearance from, the lung. After intravenous treatment with either mAb 60.3 or saline, rabbits were given an intralobar inoculation with 109 colony‐forming units of either Staphylococcus aureus or Escherichia coli. Four hours after inoculation, lungs were lavaged to assess PMN emigration. CD18 blockade reduced PMN emigration to E. coli by 76% but only 45% to S. aureus. Experiments to determine bacterial recovery from the lungs at 4, 8, and 24 h after inoculation showed that CD18 blockade impaired the early (4 h) clearance of E. coli but not S. aureus. These findings suggest that PMN emigration to intrapulmonary S. aureus is largely CD18‐independent. In contrast, intrapulmonary E. coli elicits CD18‐mediated PMN emigration. CD18 blockade results in impaired clearance of E. coli but not S. aureus from the lung. J. Leukoc. 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subjects | alveolar macrophage Animals Antibodies, Monoclonal - pharmacology CD18 Antigens - immunology Cell Adhesion - immunology Cell Movement - immunology Escherichia coli Escherichia coli Infections - immunology Escherichia coli Infections - microbiology Leukocyte Count Lung - microbiology lung lavage Neutrophils - immunology Neutrophils - microbiology Rabbits Staphylococcal Infections - immunology Staphylococcal Infections - microbiology β2 integrins |
title | CD18 adhesion blockade decreases bacterial clearance and neutrophil recruitment after intrapulmonary E. coli, but not after S. aureus |
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