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QUANTITATIVE COMPARISON OF CYTOKINE mRNA AND INFLAMMATORY RESPONSES IN CUTANEOUS LATE PHASE ALLERGIC REACTIONS
The aim of this study was to quantitatively compare expression of mRNA for IL-5 and IFN-γ with the frequency of mRNA-positive cells, total and activated eosinophils, neutrophils, lymphocytes, and vessels expressing adhesion molecules. Replicate biopsies of skin LPR to pollen antigens (Ag) and contro...
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Published in: | Cytokine (Philadelphia, Pa.) Pa.), 2000-07, Vol.12 (7), p.1065-1075 |
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description | The aim of this study was to quantitatively compare expression of mRNA for IL-5 and IFN-γ with the frequency of mRNA-positive cells, total and activated eosinophils, neutrophils, lymphocytes, and vessels expressing adhesion molecules. Replicate biopsies of skin LPR to pollen antigens (Ag) and control injection sites (B) at 6 and 24h were assessed for: (1) mRNA for IL-5 and IFN-γ by quantitative RT-PCR (QC-RT/PCR); (2) frequency of cells expressing mRNA for IL-5 and IFN-γ by in situ hybridization (ISH); (3) inflammatory cells and adhesion molecule expression. More mRNA for IL-5 was found in Ag- than in B-injected sites at 6 and 24h by both QC-RT/PCR and ISH. Small amounts of mRNA for IFN-γ were detected in Ag sites by QC-RT/PCR at 6 and 24h, but were not significantly different than at B sites. The frequency of IFN-γ mRNA+cells was higher in Ag than in B sites at 6h. There was no correlation between the amount if IL-5 detected by QC-RT/PCR and frequency of IL-5 mRNA+cells by ISH. These findings also did not correlate with the degree of inflammatory responses. In conclusion: (1) greater IL-5 than IFN-γ deposition in Ag sites suggests Th2predominance in LPR; (2) lack of correlation between QC-RT/PCR and ISH findings may reflect varying mRNA content of inflammatory cells. |
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Replicate biopsies of skin LPR to pollen antigens (Ag) and control injection sites (B) at 6 and 24h were assessed for: (1) mRNA for IL-5 and IFN-γ by quantitative RT-PCR (QC-RT/PCR); (2) frequency of cells expressing mRNA for IL-5 and IFN-γ by in situ hybridization (ISH); (3) inflammatory cells and adhesion molecule expression. More mRNA for IL-5 was found in Ag- than in B-injected sites at 6 and 24h by both QC-RT/PCR and ISH. Small amounts of mRNA for IFN-γ were detected in Ag sites by QC-RT/PCR at 6 and 24h, but were not significantly different than at B sites. The frequency of IFN-γ mRNA+cells was higher in Ag than in B sites at 6h. There was no correlation between the amount if IL-5 detected by QC-RT/PCR and frequency of IL-5 mRNA+cells by ISH. These findings also did not correlate with the degree of inflammatory responses. In conclusion: (1) greater IL-5 than IFN-γ deposition in Ag sites suggests Th2predominance in LPR; (2) lack of correlation between QC-RT/PCR and ISH findings may reflect varying mRNA content of inflammatory cells.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1006/cyto.2000.0671</identifier><identifier>PMID: 10880253</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; cutaneous late phase reactions/cytokine/IL-5/mRNA ; Dermatitis - immunology ; E-Selectin - biosynthesis ; Eosinophils - immunology ; Female ; Humans ; Hypersensitivity - immunology ; Hypersensitivity - pathology ; Immunohistochemistry - methods ; In Situ Hybridization - methods ; Interferon-gamma - biosynthesis ; Interferon-gamma - genetics ; Interleukin-5 - biosynthesis ; Interleukin-5 - genetics ; Leukocytes, Mononuclear ; Male ; Middle Aged ; Neutrophils - immunology ; Pollen - immunology ; Reverse Transcriptase Polymerase Chain Reaction - methods ; RNA, Messenger - metabolism ; Skin - immunology ; Skin - pathology ; T-Lymphocytes - immunology ; Time Factors ; Vascular Cell Adhesion Molecule-1 - biosynthesis</subject><ispartof>Cytokine (Philadelphia, Pa.), 2000-07, Vol.12 (7), p.1065-1075</ispartof><rights>2000 Academic Press</rights><rights>Copyright 2000 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-e7f7d84f44021f912a6f1833698cd1f5484c28d60065c54304af8052936878fb3</citedby><cites>FETCH-LOGICAL-c340t-e7f7d84f44021f912a6f1833698cd1f5484c28d60065c54304af8052936878fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10880253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zweiman, Burton</creatorcontrib><creatorcontrib>Parrott, Carmen M</creatorcontrib><creatorcontrib>Graif, Yael</creatorcontrib><creatorcontrib>David, Mary</creatorcontrib><creatorcontrib>Lessin, Stuart R</creatorcontrib><title>QUANTITATIVE COMPARISON OF CYTOKINE mRNA AND INFLAMMATORY RESPONSES IN CUTANEOUS LATE PHASE ALLERGIC REACTIONS</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>The aim of this study was to quantitatively compare expression of mRNA for IL-5 and IFN-γ with the frequency of mRNA-positive cells, total and activated eosinophils, neutrophils, lymphocytes, and vessels expressing adhesion molecules. Replicate biopsies of skin LPR to pollen antigens (Ag) and control injection sites (B) at 6 and 24h were assessed for: (1) mRNA for IL-5 and IFN-γ by quantitative RT-PCR (QC-RT/PCR); (2) frequency of cells expressing mRNA for IL-5 and IFN-γ by in situ hybridization (ISH); (3) inflammatory cells and adhesion molecule expression. More mRNA for IL-5 was found in Ag- than in B-injected sites at 6 and 24h by both QC-RT/PCR and ISH. Small amounts of mRNA for IFN-γ were detected in Ag sites by QC-RT/PCR at 6 and 24h, but were not significantly different than at B sites. The frequency of IFN-γ mRNA+cells was higher in Ag than in B sites at 6h. There was no correlation between the amount if IL-5 detected by QC-RT/PCR and frequency of IL-5 mRNA+cells by ISH. These findings also did not correlate with the degree of inflammatory responses. In conclusion: (1) greater IL-5 than IFN-γ deposition in Ag sites suggests Th2predominance in LPR; (2) lack of correlation between QC-RT/PCR and ISH findings may reflect varying mRNA content of inflammatory cells.</description><subject>Adult</subject><subject>cutaneous late phase reactions/cytokine/IL-5/mRNA</subject><subject>Dermatitis - immunology</subject><subject>E-Selectin - biosynthesis</subject><subject>Eosinophils - immunology</subject><subject>Female</subject><subject>Humans</subject><subject>Hypersensitivity - immunology</subject><subject>Hypersensitivity - pathology</subject><subject>Immunohistochemistry - methods</subject><subject>In Situ Hybridization - methods</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interferon-gamma - genetics</subject><subject>Interleukin-5 - biosynthesis</subject><subject>Interleukin-5 - genetics</subject><subject>Leukocytes, Mononuclear</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neutrophils - immunology</subject><subject>Pollen - immunology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>RNA, Messenger - metabolism</subject><subject>Skin - immunology</subject><subject>Skin - pathology</subject><subject>T-Lymphocytes - immunology</subject><subject>Time Factors</subject><subject>Vascular Cell Adhesion Molecule-1 - biosynthesis</subject><issn>1043-4666</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNp10E9r2zAYgHFRNtau23XHodNuzvTPsnwUntKaOXZmK4WehCtL4JHEnZUM-u0rkx522UlC_N4X9ADwBaMVRoh_ty-naUUQQivEM3wFbjDKeYIQoe-WO6MJ45xfg48h_I4qp1n2AVxjJAQiKb0Bx187WetSS10-KFg0m61sy66pYbOGxaNufpa1goe2llDWP2BZryu52UjdtI-wVd22qTvVxWdY7LSsVbPrYCW1gtt72Skoq0q1d2URqSx0GfEn8N73--A-v523YLdWurhPqiY6WSWWMnRKXOazQTDPGCLY55j03GNBKc-FHbBPmWCWiIHHAqlNGUWs9wKlJKdcZMI_0Vvw7bL3eZ7-nF04mcMYrNvv-6ObzsFkmJA0pyLC1QXaeQphdt48z-Ohn18MRmYpbJbCZilslsJx4Ovb5vPTwQ3_8EvSCMQFuPi_v6ObTbCjO1o3jLOzJzNM4_92vwIV3YAW</recordid><startdate>20000701</startdate><enddate>20000701</enddate><creator>Zweiman, Burton</creator><creator>Parrott, Carmen M</creator><creator>Graif, Yael</creator><creator>David, Mary</creator><creator>Lessin, Stuart R</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20000701</creationdate><title>QUANTITATIVE COMPARISON OF CYTOKINE mRNA AND INFLAMMATORY RESPONSES IN CUTANEOUS LATE PHASE ALLERGIC REACTIONS</title><author>Zweiman, Burton ; Parrott, Carmen M ; Graif, Yael ; David, Mary ; Lessin, Stuart R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-e7f7d84f44021f912a6f1833698cd1f5484c28d60065c54304af8052936878fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>cutaneous late phase reactions/cytokine/IL-5/mRNA</topic><topic>Dermatitis - immunology</topic><topic>E-Selectin - biosynthesis</topic><topic>Eosinophils - immunology</topic><topic>Female</topic><topic>Humans</topic><topic>Hypersensitivity - immunology</topic><topic>Hypersensitivity - pathology</topic><topic>Immunohistochemistry - methods</topic><topic>In Situ Hybridization - methods</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interferon-gamma - genetics</topic><topic>Interleukin-5 - biosynthesis</topic><topic>Interleukin-5 - genetics</topic><topic>Leukocytes, Mononuclear</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neutrophils - immunology</topic><topic>Pollen - immunology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - methods</topic><topic>RNA, Messenger - metabolism</topic><topic>Skin - immunology</topic><topic>Skin - pathology</topic><topic>T-Lymphocytes - immunology</topic><topic>Time Factors</topic><topic>Vascular Cell Adhesion Molecule-1 - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zweiman, Burton</creatorcontrib><creatorcontrib>Parrott, Carmen M</creatorcontrib><creatorcontrib>Graif, Yael</creatorcontrib><creatorcontrib>David, Mary</creatorcontrib><creatorcontrib>Lessin, Stuart R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zweiman, Burton</au><au>Parrott, Carmen M</au><au>Graif, Yael</au><au>David, Mary</au><au>Lessin, Stuart R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>QUANTITATIVE COMPARISON OF CYTOKINE mRNA AND INFLAMMATORY RESPONSES IN CUTANEOUS LATE PHASE ALLERGIC REACTIONS</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>2000-07-01</date><risdate>2000</risdate><volume>12</volume><issue>7</issue><spage>1065</spage><epage>1075</epage><pages>1065-1075</pages><issn>1043-4666</issn><eissn>1096-0023</eissn><abstract>The aim of this study was to quantitatively compare expression of mRNA for IL-5 and IFN-γ with the frequency of mRNA-positive cells, total and activated eosinophils, neutrophils, lymphocytes, and vessels expressing adhesion molecules. Replicate biopsies of skin LPR to pollen antigens (Ag) and control injection sites (B) at 6 and 24h were assessed for: (1) mRNA for IL-5 and IFN-γ by quantitative RT-PCR (QC-RT/PCR); (2) frequency of cells expressing mRNA for IL-5 and IFN-γ by in situ hybridization (ISH); (3) inflammatory cells and adhesion molecule expression. More mRNA for IL-5 was found in Ag- than in B-injected sites at 6 and 24h by both QC-RT/PCR and ISH. Small amounts of mRNA for IFN-γ were detected in Ag sites by QC-RT/PCR at 6 and 24h, but were not significantly different than at B sites. The frequency of IFN-γ mRNA+cells was higher in Ag than in B sites at 6h. There was no correlation between the amount if IL-5 detected by QC-RT/PCR and frequency of IL-5 mRNA+cells by ISH. These findings also did not correlate with the degree of inflammatory responses. In conclusion: (1) greater IL-5 than IFN-γ deposition in Ag sites suggests Th2predominance in LPR; (2) lack of correlation between QC-RT/PCR and ISH findings may reflect varying mRNA content of inflammatory cells.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>10880253</pmid><doi>10.1006/cyto.2000.0671</doi><tpages>11</tpages></addata></record> |
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subjects | Adult cutaneous late phase reactions/cytokine/IL-5/mRNA Dermatitis - immunology E-Selectin - biosynthesis Eosinophils - immunology Female Humans Hypersensitivity - immunology Hypersensitivity - pathology Immunohistochemistry - methods In Situ Hybridization - methods Interferon-gamma - biosynthesis Interferon-gamma - genetics Interleukin-5 - biosynthesis Interleukin-5 - genetics Leukocytes, Mononuclear Male Middle Aged Neutrophils - immunology Pollen - immunology Reverse Transcriptase Polymerase Chain Reaction - methods RNA, Messenger - metabolism Skin - immunology Skin - pathology T-Lymphocytes - immunology Time Factors Vascular Cell Adhesion Molecule-1 - biosynthesis |
title | QUANTITATIVE COMPARISON OF CYTOKINE mRNA AND INFLAMMATORY RESPONSES IN CUTANEOUS LATE PHASE ALLERGIC REACTIONS |
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