Histology and immunohistology of Igh-1-restricted herpes simplex keratitis in BALB/c congenic mice
In order to characterize the local ocular immunologic milieu of Igh-1-restricted herpes simplex keratitis (HSK), we investigated histologic and immunohistologic correlates of disease over a 21-day time course. Clinically observable keratitis began 10 days postinoculation in susceptible C.AL-20 (Igh-...
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Veröffentlicht in: | Investigative ophthalmology & visual science 1990-02, Vol.31 (2), p.305-312 |
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description | In order to characterize the local ocular immunologic milieu of Igh-1-restricted herpes simplex keratitis (HSK), we investigated histologic and immunohistologic correlates of disease over a 21-day time course. Clinically observable keratitis began 10 days postinoculation in susceptible C.AL-20 (Igh-1d) and moderately susceptible BALB/c (Igh-1a) mice, whereas HSV-1-resistant C.B-17 (Igh-1b) mice rarely developed disease. Igh-1-restricted histologic differences were observed by day 11 postinoculation; C.AL-20 and BALB/c mice showed augmented recruitment of neutrophils and mononuclear cells in conjunctival, limbal, and corneal tissues compared to C.B-17 mice. On immunohistologic study, Lyt-1 to Lyt-2 cell ratios by day 11 postinoculation were 7:1, 2:1, and 1:8 in corneas from C.AL-20, BALB/c, and C.B-17 mice, respectively. Macrophages and neutrophils were absent in corneas from C.B-17 mice at this time, but could be found in large numbers in the corneas of susceptible mouse strains through day 21. These data demonstrate a strong relationship between Igh-1 phenotype and inflammatory cell recruitment in response to corneal infection with HSV-1, and support a role for T cell subpopulations in mediating Igh-1-restricted HSK. |
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Clinically observable keratitis began 10 days postinoculation in susceptible C.AL-20 (Igh-1d) and moderately susceptible BALB/c (Igh-1a) mice, whereas HSV-1-resistant C.B-17 (Igh-1b) mice rarely developed disease. Igh-1-restricted histologic differences were observed by day 11 postinoculation; C.AL-20 and BALB/c mice showed augmented recruitment of neutrophils and mononuclear cells in conjunctival, limbal, and corneal tissues compared to C.B-17 mice. On immunohistologic study, Lyt-1 to Lyt-2 cell ratios by day 11 postinoculation were 7:1, 2:1, and 1:8 in corneas from C.AL-20, BALB/c, and C.B-17 mice, respectively. Macrophages and neutrophils were absent in corneas from C.B-17 mice at this time, but could be found in large numbers in the corneas of susceptible mouse strains through day 21. These data demonstrate a strong relationship between Igh-1 phenotype and inflammatory cell recruitment in response to corneal infection with HSV-1, and support a role for T cell subpopulations in mediating Igh-1-restricted HSK.</description><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>PMID: 2154415</identifier><identifier>CODEN: IOVSDA</identifier><language>eng</language><publisher>Rockville, MD: ARVO</publisher><subject>Animals ; Biological and medical sciences ; Cornea - immunology ; Cornea - pathology ; Experimental viral diseases and models ; Immunoenzyme Techniques ; Immunoglobulin Heavy Chains - genetics ; Infectious diseases ; Keratitis, Dendritic - genetics ; Keratitis, Dendritic - immunology ; Keratitis, Dendritic - pathology ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Neutrophils - immunology ; Phenotype ; Simplexvirus - immunology ; Viral diseases</subject><ispartof>Investigative ophthalmology & visual science, 1990-02, Vol.31 (2), p.305-312</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19268340$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2154415$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Opremcak, EM</creatorcontrib><creatorcontrib>Rice, BA</creatorcontrib><creatorcontrib>Wells, PA</creatorcontrib><creatorcontrib>Foster, CS</creatorcontrib><title>Histology and immunohistology of Igh-1-restricted herpes simplex keratitis in BALB/c congenic mice</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>In order to characterize the local ocular immunologic milieu of Igh-1-restricted herpes simplex keratitis (HSK), we investigated histologic and immunohistologic correlates of disease over a 21-day time course. Clinically observable keratitis began 10 days postinoculation in susceptible C.AL-20 (Igh-1d) and moderately susceptible BALB/c (Igh-1a) mice, whereas HSV-1-resistant C.B-17 (Igh-1b) mice rarely developed disease. Igh-1-restricted histologic differences were observed by day 11 postinoculation; C.AL-20 and BALB/c mice showed augmented recruitment of neutrophils and mononuclear cells in conjunctival, limbal, and corneal tissues compared to C.B-17 mice. On immunohistologic study, Lyt-1 to Lyt-2 cell ratios by day 11 postinoculation were 7:1, 2:1, and 1:8 in corneas from C.AL-20, BALB/c, and C.B-17 mice, respectively. Macrophages and neutrophils were absent in corneas from C.B-17 mice at this time, but could be found in large numbers in the corneas of susceptible mouse strains through day 21. These data demonstrate a strong relationship between Igh-1 phenotype and inflammatory cell recruitment in response to corneal infection with HSV-1, and support a role for T cell subpopulations in mediating Igh-1-restricted HSK.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cornea - immunology</subject><subject>Cornea - pathology</subject><subject>Experimental viral diseases and models</subject><subject>Immunoenzyme Techniques</subject><subject>Immunoglobulin Heavy Chains - genetics</subject><subject>Infectious diseases</subject><subject>Keratitis, Dendritic - genetics</subject><subject>Keratitis, Dendritic - immunology</subject><subject>Keratitis, Dendritic - pathology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Neutrophils - immunology</subject><subject>Phenotype</subject><subject>Simplexvirus - immunology</subject><subject>Viral diseases</subject><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLw0AUhQdRaq3-BGE2ugvOO51lW9QWCm50HSaTm2Q0L2cSYv-9AYMu5SwunPNxuJwztKRSskjGa36OloQKFRFBxCW6CuGdEEYpIwu0YFQKQeUSpXsX-rZqixM2TYZdXQ9NW_56bY4PRRnRyEPovbM9ZLgE30HAwdVdBV_4A7zpXe8Cdg3ebo7bB4tt2xTQOItrZ-EaXeSmCnAz3xV6e3p83e2j48vzYbc5RiXTcR9RZYgwhmilVUxZmq6zNFWaZlZwk_HcgpSgmJUi0_EaUsVlzonNcxLHKQXBV-j-p7fz7ecw_ZvULlioKtNAO4Qk1ooKzuN_QSo14XrSCt3O4JDWkCWdd7Xxp2Reb8rv5twEa6rcm8a68ItRzdSaC_LHla4oR-chCbWpqqmVJuM4cpqwhBPJvwFbG4Z9</recordid><startdate>19900201</startdate><enddate>19900201</enddate><creator>Opremcak, EM</creator><creator>Rice, BA</creator><creator>Wells, PA</creator><creator>Foster, CS</creator><general>ARVO</general><general>Association for Research in Vision and Ophtalmology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19900201</creationdate><title>Histology and immunohistology of Igh-1-restricted herpes simplex keratitis in BALB/c congenic mice</title><author>Opremcak, EM ; Rice, BA ; Wells, PA ; Foster, CS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h297t-16a04aa09696712bb8dbb691dc43ad3fce55e62c54d978eb635f30cff077b1e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cornea - immunology</topic><topic>Cornea - pathology</topic><topic>Experimental viral diseases and models</topic><topic>Immunoenzyme Techniques</topic><topic>Immunoglobulin Heavy Chains - genetics</topic><topic>Infectious diseases</topic><topic>Keratitis, Dendritic - genetics</topic><topic>Keratitis, Dendritic - immunology</topic><topic>Keratitis, Dendritic - pathology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Neutrophils - immunology</topic><topic>Phenotype</topic><topic>Simplexvirus - immunology</topic><topic>Viral diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Opremcak, EM</creatorcontrib><creatorcontrib>Rice, BA</creatorcontrib><creatorcontrib>Wells, PA</creatorcontrib><creatorcontrib>Foster, CS</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Opremcak, EM</au><au>Rice, BA</au><au>Wells, PA</au><au>Foster, CS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histology and immunohistology of Igh-1-restricted herpes simplex keratitis in BALB/c congenic mice</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>1990-02-01</date><risdate>1990</risdate><volume>31</volume><issue>2</issue><spage>305</spage><epage>312</epage><pages>305-312</pages><issn>0146-0404</issn><eissn>1552-5783</eissn><coden>IOVSDA</coden><abstract>In order to characterize the local ocular immunologic milieu of Igh-1-restricted herpes simplex keratitis (HSK), we investigated histologic and immunohistologic correlates of disease over a 21-day time course. Clinically observable keratitis began 10 days postinoculation in susceptible C.AL-20 (Igh-1d) and moderately susceptible BALB/c (Igh-1a) mice, whereas HSV-1-resistant C.B-17 (Igh-1b) mice rarely developed disease. Igh-1-restricted histologic differences were observed by day 11 postinoculation; C.AL-20 and BALB/c mice showed augmented recruitment of neutrophils and mononuclear cells in conjunctival, limbal, and corneal tissues compared to C.B-17 mice. On immunohistologic study, Lyt-1 to Lyt-2 cell ratios by day 11 postinoculation were 7:1, 2:1, and 1:8 in corneas from C.AL-20, BALB/c, and C.B-17 mice, respectively. Macrophages and neutrophils were absent in corneas from C.B-17 mice at this time, but could be found in large numbers in the corneas of susceptible mouse strains through day 21. These data demonstrate a strong relationship between Igh-1 phenotype and inflammatory cell recruitment in response to corneal infection with HSV-1, and support a role for T cell subpopulations in mediating Igh-1-restricted HSK.</abstract><cop>Rockville, MD</cop><pub>ARVO</pub><pmid>2154415</pmid><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cornea - immunology Cornea - pathology Experimental viral diseases and models Immunoenzyme Techniques Immunoglobulin Heavy Chains - genetics Infectious diseases Keratitis, Dendritic - genetics Keratitis, Dendritic - immunology Keratitis, Dendritic - pathology Medical sciences Mice Mice, Inbred BALB C Neutrophils - immunology Phenotype Simplexvirus - immunology Viral diseases |
title | Histology and immunohistology of Igh-1-restricted herpes simplex keratitis in BALB/c congenic mice |
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