Natural killer cell function in children with malignant solid neoplasias
Natural killer (NK) cell numbers and lytic activity were determined in 40 children with various types of solid malignant neoplasias and in 25 control children by NKH‐1 monoclonal antibody and cytotoxicity against K562 target cells, respectively. Patients were analyzed at the time of diagnosis before...
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Veröffentlicht in: | Medical and pediatric oncology 1991, Vol.19 (3), p.175-181 |
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description | Natural killer (NK) cell numbers and lytic activity were determined in 40 children with various types of solid malignant neoplasias and in 25 control children by NKH‐1 monoclonal antibody and cytotoxicity against K562 target cells, respectively. Patients were analyzed at the time of diagnosis before initiation of therapy and followed over a median time of 15.8 months. Mean NK cell numbers and lytic activity were similar among different types of tumor analyzed. Patients with localized disease (stages I, II; n = 25) also showed values not statistically different from those of patients in advanced disease (stages III, IV; n = 15). According to their response to therapy, patients were divided into three groups: group 1 (complete remission; n = 28), group 2 (partial remission; n = 5), and group 3 (progression of disease; n = 6). Patients in group 3 showed at the time of diagnosis a mean NK activity significantly lower than that of patients in groups 1 and 2 and control children (P = 0.007). The defect in NK cell lytic capacity in vitro observed in patients with progressive disease suggests that NK cells play a role in the control of neoplasic growth in vivo and may imply that some children with refractory progressive disease can benefit from immu‐nomodulation destined to improve the lytic potential of NK cells. |
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Patients were analyzed at the time of diagnosis before initiation of therapy and followed over a median time of 15.8 months. Mean NK cell numbers and lytic activity were similar among different types of tumor analyzed. Patients with localized disease (stages I, II; n = 25) also showed values not statistically different from those of patients in advanced disease (stages III, IV; n = 15). According to their response to therapy, patients were divided into three groups: group 1 (complete remission; n = 28), group 2 (partial remission; n = 5), and group 3 (progression of disease; n = 6). Patients in group 3 showed at the time of diagnosis a mean NK activity significantly lower than that of patients in groups 1 and 2 and control children (P = 0.007). The defect in NK cell lytic capacity in vitro observed in patients with progressive disease suggests that NK cells play a role in the control of neoplasic growth in vivo and may imply that some children with refractory progressive disease can benefit from immu‐nomodulation destined to improve the lytic potential of NK cells.</description><identifier>ISSN: 0098-1532</identifier><identifier>EISSN: 1096-911X</identifier><identifier>DOI: 10.1002/mpo.2950190306</identifier><identifier>PMID: 2023566</identifier><identifier>CODEN: MPONDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Child ; Child, Preschool ; Cytotoxicity, Immunologic - drug effects ; Female ; Follow-Up Studies ; Humans ; Infant ; Killer Cells, Natural - drug effects ; Killer Cells, Natural - immunology ; Killer Cells, Natural - pathology ; Leukocyte Count ; Male ; Medical sciences ; natural killer activity ; Neoplasm Staging ; Neoplasms - drug therapy ; Neoplasms - immunology ; Neoplasms - pathology ; NK cells ; NKH-1 antigen ; Prognosis ; Regression Analysis ; Remission Induction ; Survival Rate ; Tumors</subject><ispartof>Medical and pediatric oncology, 1991, Vol.19 (3), p.175-181</ispartof><rights>Copyright © 1991 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1992 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4076-8281013de4b4f4944b0cdeeab6146648b5845b7be1da1102147145154f047ecd3</citedby><cites>FETCH-LOGICAL-c4076-8281013de4b4f4944b0cdeeab6146648b5845b7be1da1102147145154f047ecd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmpo.2950190306$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmpo.2950190306$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4009,27902,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5475012$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2023566$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gallego-Melcón, Soledad</creatorcontrib><creatorcontrib>Boren, Teresa Español</creatorcontrib><creatorcontrib>de Toledo, Jose Sanchez</creatorcontrib><creatorcontrib>Viñas, Jorge Prats</creatorcontrib><title>Natural killer cell function in children with malignant solid neoplasias</title><title>Medical and pediatric oncology</title><addtitle>Med. Pediatr. Oncol</addtitle><description>Natural killer (NK) cell numbers and lytic activity were determined in 40 children with various types of solid malignant neoplasias and in 25 control children by NKH‐1 monoclonal antibody and cytotoxicity against K562 target cells, respectively. Patients were analyzed at the time of diagnosis before initiation of therapy and followed over a median time of 15.8 months. Mean NK cell numbers and lytic activity were similar among different types of tumor analyzed. Patients with localized disease (stages I, II; n = 25) also showed values not statistically different from those of patients in advanced disease (stages III, IV; n = 15). According to their response to therapy, patients were divided into three groups: group 1 (complete remission; n = 28), group 2 (partial remission; n = 5), and group 3 (progression of disease; n = 6). Patients in group 3 showed at the time of diagnosis a mean NK activity significantly lower than that of patients in groups 1 and 2 and control children (P = 0.007). The defect in NK cell lytic capacity in vitro observed in patients with progressive disease suggests that NK cells play a role in the control of neoplasic growth in vivo and may imply that some children with refractory progressive disease can benefit from immu‐nomodulation destined to improve the lytic potential of NK cells.</description><subject>Adolescent</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cytotoxicity, Immunologic - drug effects</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Killer Cells, Natural - drug effects</subject><subject>Killer Cells, Natural - immunology</subject><subject>Killer Cells, Natural - pathology</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Medical sciences</subject><subject>natural killer activity</subject><subject>Neoplasm Staging</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - pathology</subject><subject>NK cells</subject><subject>NKH-1 antigen</subject><subject>Prognosis</subject><subject>Regression Analysis</subject><subject>Remission Induction</subject><subject>Survival Rate</subject><subject>Tumors</subject><issn>0098-1532</issn><issn>1096-911X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1P3DAQxS3UChbKlRuSD1Vv2c74K_GxQi1QLR-HVq16sRzHARcnWexElP-eoF1t1VNPo9H83punR8gJwhIB2MduPSyZloAaOKg9skDQqtCIP9-QBYCuCpScHZDDnH_DvOuy2if7DBiXSi3IxbUdp2QjfQgx-kSdj5G2U-_GMPQ09NTdh9gk39OnMN7TzsZw19t-pHmIoaG9H9bR5mDzO_K2tTH74-08It-_fP52dlGsbs4vzz6tCiegVEXFKgTkjRe1aIUWogbXeG9rhUIpUdWyErIua4-NRQSGokQhUYoWROldw4_Ih43vOg2Pk8-j6UJ-TW3nLFM2FUguOMIMLjegS0POybdmnUJn07NBMK_Vmbk687e6WXC6dZ7qzjc7fNvVfH-_vdvsbGyT7V3IO0yKcrZiM6Y32FOI_vk_T83V7c0_EYqNNuTR_9lpbXowquSlND-uzw0Tv_TX1erKSP4CqBKVnA</recordid><startdate>1991</startdate><enddate>1991</enddate><creator>Gallego-Melcón, Soledad</creator><creator>Boren, Teresa Español</creator><creator>de Toledo, Jose Sanchez</creator><creator>Viñas, Jorge Prats</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><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>1991</creationdate><title>Natural killer cell function in children with malignant solid neoplasias</title><author>Gallego-Melcón, Soledad ; Boren, Teresa Español ; de Toledo, Jose Sanchez ; Viñas, Jorge Prats</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4076-8281013de4b4f4944b0cdeeab6146648b5845b7be1da1102147145154f047ecd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Adolescent</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cytotoxicity, Immunologic - drug effects</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Killer Cells, Natural - drug effects</topic><topic>Killer Cells, Natural - immunology</topic><topic>Killer Cells, Natural - pathology</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Medical sciences</topic><topic>natural killer activity</topic><topic>Neoplasm Staging</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - pathology</topic><topic>NK cells</topic><topic>NKH-1 antigen</topic><topic>Prognosis</topic><topic>Regression Analysis</topic><topic>Remission Induction</topic><topic>Survival Rate</topic><topic>Tumors</topic><toplevel>online_resources</toplevel><creatorcontrib>Gallego-Melcón, Soledad</creatorcontrib><creatorcontrib>Boren, Teresa Español</creatorcontrib><creatorcontrib>de Toledo, Jose Sanchez</creatorcontrib><creatorcontrib>Viñas, Jorge Prats</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Medical and pediatric oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallego-Melcón, Soledad</au><au>Boren, Teresa Español</au><au>de Toledo, Jose Sanchez</au><au>Viñas, Jorge Prats</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural killer cell function in children with malignant solid neoplasias</atitle><jtitle>Medical and pediatric oncology</jtitle><addtitle>Med. Pediatr. Oncol</addtitle><date>1991</date><risdate>1991</risdate><volume>19</volume><issue>3</issue><spage>175</spage><epage>181</epage><pages>175-181</pages><issn>0098-1532</issn><eissn>1096-911X</eissn><coden>MPONDB</coden><abstract>Natural killer (NK) cell numbers and lytic activity were determined in 40 children with various types of solid malignant neoplasias and in 25 control children by NKH‐1 monoclonal antibody and cytotoxicity against K562 target cells, respectively. Patients were analyzed at the time of diagnosis before initiation of therapy and followed over a median time of 15.8 months. Mean NK cell numbers and lytic activity were similar among different types of tumor analyzed. Patients with localized disease (stages I, II; n = 25) also showed values not statistically different from those of patients in advanced disease (stages III, IV; n = 15). According to their response to therapy, patients were divided into three groups: group 1 (complete remission; n = 28), group 2 (partial remission; n = 5), and group 3 (progression of disease; n = 6). Patients in group 3 showed at the time of diagnosis a mean NK activity significantly lower than that of patients in groups 1 and 2 and control children (P = 0.007). The defect in NK cell lytic capacity in vitro observed in patients with progressive disease suggests that NK cells play a role in the control of neoplasic growth in vivo and may imply that some children with refractory progressive disease can benefit from immu‐nomodulation destined to improve the lytic potential of NK cells.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2023566</pmid><doi>10.1002/mpo.2950190306</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Child Child, Preschool Cytotoxicity, Immunologic - drug effects Female Follow-Up Studies Humans Infant Killer Cells, Natural - drug effects Killer Cells, Natural - immunology Killer Cells, Natural - pathology Leukocyte Count Male Medical sciences natural killer activity Neoplasm Staging Neoplasms - drug therapy Neoplasms - immunology Neoplasms - pathology NK cells NKH-1 antigen Prognosis Regression Analysis Remission Induction Survival Rate Tumors |
title | Natural killer cell function in children with malignant solid neoplasias |
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