Alternative pathway of complement activation in full term and premature infants
Classical and alternative pathway complement levels were measured in the cord blood sera of 60 newly born infants, with weights ranging from 1200--4165 g. The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B,...
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Veröffentlicht in: | Pediatric research 1979-05, Vol.13 (5 Pt 1), p.641-643 |
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description | Classical and alternative pathway complement levels were measured in the cord blood sera of 60 newly born infants, with weights ranging from 1200--4165 g. The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B, and properdin were all significantly less than normal adult levels (P less than 0.0001). All of the above determinations were significantly correlated with one another except for the relationship between properdin and factor B. CH50, PH50, C4, and properdin levels were significantly correlated with birth weight although there was much residual scatter. Neither maternal illness nor mild to moderate illness in the newborn altered the birth weight-complement relationships. Severe infant illness did significantly alter the relationship between birth weight and complement. However, the impact of this variable on the birth weight-complement relationships was not consistent among the various components. These inconsistencies and the small sample size preclude drawing any strong conclusions about severe illness and complement levels. |
doi_str_mv | 10.1203/00006450-197905000-00013 |
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The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B, and properdin were all significantly less than normal adult levels (P less than 0.0001). All of the above determinations were significantly correlated with one another except for the relationship between properdin and factor B. CH50, PH50, C4, and properdin levels were significantly correlated with birth weight although there was much residual scatter. Neither maternal illness nor mild to moderate illness in the newborn altered the birth weight-complement relationships. Severe infant illness did significantly alter the relationship between birth weight and complement. However, the impact of this variable on the birth weight-complement relationships was not consistent among the various components. These inconsistencies and the small sample size preclude drawing any strong conclusions about severe illness and complement levels.</description><identifier>ISSN: 0031-3998</identifier><identifier>EISSN: 1530-0447</identifier><identifier>DOI: 10.1203/00006450-197905000-00013</identifier><identifier>PMID: 471596</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Birth Weight ; Complement Activation ; Complement Pathway, Alternative ; Female ; Humans ; Infant, Newborn ; Infant, Newborn, Diseases - immunology ; Infant, Premature ; Pregnancy ; Pregnancy Complications</subject><ispartof>Pediatric research, 1979-05, Vol.13 (5 Pt 1), p.641-643</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-bd27751fd15a6b55c0e7c6f2674b068ce14acee40475d20d126ee17500b00c93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/471596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Strunk, R C</creatorcontrib><creatorcontrib>Fenton, L J</creatorcontrib><creatorcontrib>Gaines, J A</creatorcontrib><title>Alternative pathway of complement activation in full term and premature infants</title><title>Pediatric research</title><addtitle>Pediatr Res</addtitle><description>Classical and alternative pathway complement levels were measured in the cord blood sera of 60 newly born infants, with weights ranging from 1200--4165 g. The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B, and properdin were all significantly less than normal adult levels (P less than 0.0001). All of the above determinations were significantly correlated with one another except for the relationship between properdin and factor B. CH50, PH50, C4, and properdin levels were significantly correlated with birth weight although there was much residual scatter. Neither maternal illness nor mild to moderate illness in the newborn altered the birth weight-complement relationships. Severe infant illness did significantly alter the relationship between birth weight and complement. However, the impact of this variable on the birth weight-complement relationships was not consistent among the various components. These inconsistencies and the small sample size preclude drawing any strong conclusions about severe illness and complement levels.</description><subject>Adult</subject><subject>Birth Weight</subject><subject>Complement Activation</subject><subject>Complement Pathway, Alternative</subject><subject>Female</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Newborn, Diseases - immunology</subject><subject>Infant, Premature</subject><subject>Pregnancy</subject><subject>Pregnancy Complications</subject><issn>0031-3998</issn><issn>1530-0447</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1PwzAMhiPE1xj8Aw45cSskTdK0x2niS5q0y-5RmjqiKE1LkoL27wlsYMmyLL-vLT8IYUruaUnYA8lRcUEK2siGiNwVOSk7QQsqWG44l6doQQijBWua-hJdxfieFVzU_AKdc0lFUy3QduUSBK9T_wl40untS-_xaLEZh8nBAD5hbfIwC0aPe4_t7BzOlgFr3-EpwKDTHCCPrPYpXqMzq12Em2Ndot3T4279Umy2z6_r1aYwTDSpaLtSSkFtR4WuWiEMAWkqW1aSt6SqDVCuDQAnXIquJB0tKwAq858tIaZhS3R3WDuF8WOGmNTQRwPOaQ_jHJXM_9FSsiysD0ITxhgDWDWFftBhryhRPyTVH0n1T1L9kszW2-ONuR2g-zce0LFvGi1uvw</recordid><startdate>197905</startdate><enddate>197905</enddate><creator>Strunk, R C</creator><creator>Fenton, L J</creator><creator>Gaines, J A</creator><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>197905</creationdate><title>Alternative pathway of complement activation in full term and premature infants</title><author>Strunk, R C ; Fenton, L J ; Gaines, J A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-bd27751fd15a6b55c0e7c6f2674b068ce14acee40475d20d126ee17500b00c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>Adult</topic><topic>Birth Weight</topic><topic>Complement Activation</topic><topic>Complement Pathway, Alternative</topic><topic>Female</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Newborn, Diseases - immunology</topic><topic>Infant, Premature</topic><topic>Pregnancy</topic><topic>Pregnancy Complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strunk, R C</creatorcontrib><creatorcontrib>Fenton, L J</creatorcontrib><creatorcontrib>Gaines, J A</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>Pediatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strunk, R C</au><au>Fenton, L J</au><au>Gaines, J A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alternative pathway of complement activation in full term and premature infants</atitle><jtitle>Pediatric research</jtitle><addtitle>Pediatr Res</addtitle><date>1979-05</date><risdate>1979</risdate><volume>13</volume><issue>5 Pt 1</issue><spage>641</spage><epage>643</epage><pages>641-643</pages><issn>0031-3998</issn><eissn>1530-0447</eissn><abstract>Classical and alternative pathway complement levels were measured in the cord blood sera of 60 newly born infants, with weights ranging from 1200--4165 g. The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B, and properdin were all significantly less than normal adult levels (P less than 0.0001). All of the above determinations were significantly correlated with one another except for the relationship between properdin and factor B. CH50, PH50, C4, and properdin levels were significantly correlated with birth weight although there was much residual scatter. Neither maternal illness nor mild to moderate illness in the newborn altered the birth weight-complement relationships. Severe infant illness did significantly alter the relationship between birth weight and complement. However, the impact of this variable on the birth weight-complement relationships was not consistent among the various components. These inconsistencies and the small sample size preclude drawing any strong conclusions about severe illness and complement levels.</abstract><cop>United States</cop><pmid>471596</pmid><doi>10.1203/00006450-197905000-00013</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; SpringerLink Journals - AutoHoldings; Journals@Ovid Complete |
subjects | Adult Birth Weight Complement Activation Complement Pathway, Alternative Female Humans Infant, Newborn Infant, Newborn, Diseases - immunology Infant, Premature Pregnancy Pregnancy Complications |
title | Alternative pathway of complement activation in full term and premature infants |
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