<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1025-028X</journal-id>
<journal-title><![CDATA[Vaccimonitor]]></journal-title>
<abbrev-journal-title><![CDATA[Vaccimonitor]]></abbrev-journal-title>
<issn>1025-028X</issn>
<publisher>
<publisher-name><![CDATA[Finlay Ediciones]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1025-028X2003000300002</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Estudio de los tumores sólidos desarrollados por los ratones durante la producción de Anticuerpos Monoclonales]]></article-title>
<article-title xml:lang="en"><![CDATA[Study of Solid Tumors developed by mice during the production of Monoclonal Antibodies]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fuentes Morales]]></surname>
<given-names><![CDATA[Dasha]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[González Pumarino]]></surname>
<given-names><![CDATA[Ramiro R]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[González Navarro]]></surname>
<given-names><![CDATA[Bárbara O]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Negrín Rodríguez]]></surname>
<given-names><![CDATA[Natacha]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Centro Nacional para la Producción de Animales de Laboratorio  ]]></institution>
<addr-line><![CDATA[La Habana ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2003</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2003</year>
</pub-date>
<volume>12</volume>
<numero>3</numero>
<fpage>11</fpage>
<lpage>17</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1025-028X2003000300002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1025-028X2003000300002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1025-028X2003000300002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Los ratones constituyen un elemento fundamental para la producción de líquido ascítico rico en anticuerpos monoclonales (AcM). Durante este proceso suelen aparecer tumores sólidos que afectan directamente el volumen de producción, por lo que el objetivo de este trabajo consistió en estudiar estas neoformaciones para establecer sus características y de esta manera poder predecir las afectaciones en la producción a escala industrial de líquido ascítico. Se utilizó la información de 12 250 animales de ambos sexos agrupados en 12 lotes de producción de los hibridomas CB-HEP.1,IOR r3 e IOR t1, determinando el momento de aparición, la incidencia de tumores por sexos e hibridomas, así como sus características anatomopatológicas. Se demostró que los tumores comienzan a aparecer a partir del día 14 postinoculación, llegando a afectar al 3,4% de los animales el día 20 postinoculación, existiendo diferencias significativas (p<0,05) en la frecuencia de aparición en los machos respecto a las hembras (4,4% vs 2,3%). Además, se observó mayor incidencia del hibridoma CB-HEP.1, seguido de ior t1 e ior r3 (3,9%, 1% y 0,3%, respectivamente). El análisis histopatológico reveló que se trata de una discrasia de células plasmáticas, es decir, mielomas que van creciendo pudiendo llegar a ocupar toda la cavidad peritoneal y limitar la recolección y producción del líquido ascítico.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Mice are one of the most important elements in the production of ascitic fluid. Solid tumors can occur during this process. The objective of this work was to characterize such tumors, in order to predict their effect on production. The information used, was obtained from the study of 12 250 animals, both males and females, grouped into 12 production batches of CB-HEP.1, ior r3 and ior t1 hybridomas. The time of tumor emergence, the incidence by sex and hybridoma type, as well as their anatomopathological characteristics were determined. Tumors were evident starting on day 14th after the inoculation, affecting 3.4% of mice by the 20th day post-inoculation. There were significant differences (p<0.05) between sexes (4.4% males and 2.3% females). In addition, a higher solid tumor incidence (3.87%) was detected with the CB-HEP.1 hybridoma. The histological analysis showed a plasmatic cell dyscrasia.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[ratones]]></kwd>
<kwd lng="es"><![CDATA[producción de ascitis]]></kwd>
<kwd lng="es"><![CDATA[tumores sólidos]]></kwd>
<kwd lng="en"><![CDATA[Mice]]></kwd>
<kwd lng="en"><![CDATA[ascitis production]]></kwd>
<kwd lng="en"><![CDATA[solid tumors]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><font size="2" face="Verdana"><strong>ARTICULOS ORIGINALES</strong></font></p>     <p align="justify">&nbsp;</p>     <p align="right"><font size="4" face="Verdana"><strong>Estudio de los tumores s&oacute;lidos desarrollados por los   ratones durante la producci&oacute;n de Anticuerpos   Monoclonales<br /> </strong></font></p>     <p align="right">&nbsp;</p>     <p align="right"><strong><font size="3" face="Verdana">A Study of Solid Tumors developed by mice during the production of Monoclonal   Antibodies.</font></strong></p>     <p align="justify">&nbsp;</p>     <p align="justify"><strong><font size="2" face="Verdana">Dasha Fuentes Morales, Ramiro R. Gonz&aacute;lez Pumarino, B&aacute;rbara O. Gonz&aacute;lez Navarro, Natacha Negr&iacute;n   Rodr&iacute;guez.</font></strong><font size="2" face="Verdana"><br /> </font></p>     <p><font size="2" face="Verdana">Centro Nacional para la Producci&oacute;n de Animales de Laboratorio, CENPALAB. Finca Tirabeque, Km 2&frac12;   Carretera al Cacahual,Bejucal.La Habana.Cuba.E-mail: <a href="emailto:mail@cenpalab.inf.cu">mail@cenpalab.inf.cu</a><br />  </font></p> <hr align="JUSTIFY" />     <p align="justify"><font size="2" face="Verdana"><strong>RESUMEN</strong></font></p>     <p align="justify"><font size="2" face="Verdana">Los ratones constituyen un elemento fundamental para la producci&oacute;n de l&iacute;quido asc&iacute;tico rico en   anticuerpos monoclonales (AcM). Durante este proceso suelen aparecer tumores s&oacute;lidos que afectan   directamente el volumen de producci&oacute;n, por lo que el objetivo de este trabajo consisti&oacute; en estudiar   estas neoformaciones para establecer sus caracter&iacute;sticas y de esta manera poder predecir las   afectaciones en la producci&oacute;n a escala industrial de l&iacute;quido asc&iacute;tico. Se utiliz&oacute; la informaci&oacute;n de   12 250 animales de ambos sexos agrupados en 12 lotes de producci&oacute;n de los hibridomas CB-HEP.1,IOR r3 e IOR t1, determinando el momento de aparici&oacute;n, la incidencia de tumores por sexos e<br />  hibridomas, as&iacute; como sus caracter&iacute;sticas anatomopatol&oacute;gicas. Se demostr&oacute; que los tumores   comienzan a aparecer a partir del d&iacute;a 14 postinoculaci&oacute;n, llegando a afectar al 3,4% de los animales   el d&iacute;a 20 postinoculaci&oacute;n, existiendo diferencias significativas (p&lt;0,05) en la frecuencia de aparici&oacute;n   en los machos respecto a las hembras (4,4% vs 2,3%). Adem&aacute;s, se observ&oacute; mayor incidencia del   hibridoma CB-HEP.1, seguido de ior t1 e ior r3 (3,9%, 1% y 0,3%, respectivamente). El an&aacute;lisis   histopatol&oacute;gico revel&oacute; que se trata de una discrasia de c&eacute;lulas plasm&aacute;ticas, es decir, mielomas que   van creciendo pudiendo llegar a ocupar toda la cavidad peritoneal y limitar la recolecci&oacute;n y   producci&oacute;n del l&iacute;quido asc&iacute;tico.<br /> </font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font size="2" face="Verdana"><strong>Palabras claves:</strong> ratones; producci&oacute;n de ascitis; tumores s&oacute;lidos.</font></p> <hr align="JUSTIFY" />     <p align="justify"><font size="2" face="Verdana"> <strong>ABSTRACT</strong></font></p>     <p align="justify"><font size="2" face="Verdana"> Mice are one of the most important elements in the production of ascitic fluid. Solid tumors can occur during   this process. The objective of this work was to characterize such tumors, in order to predict their effect on   production. The information used, was obtained from the study of 12 250 animals, both males and females,   grouped into 12 production batches of CB-HEP.1, ior r3 and ior t1 hybridomas. The time of tumor   emergence, the incidence by sex and hybridoma type, as well as their anatomopathological characteristics   were determined. Tumors were evident starting on day 14th after the inoculation, affecting 3.4% of mice by   the 20th day post-inoculation. There were significant differences (p&lt;0.05) between sexes (4.4% males and   2.3% females). In addition, a higher solid tumor incidence (3.87%) was detected with the CB-HEP.1   hybridoma. The histological analysis showed a plasmatic cell dyscrasia.<br /> </font></p>     <p align="justify"><font size="2" face="Verdana"><strong>Keywords:</strong> Mice, ascitis production, solid tumors.</font></p> <hr align="JUSTIFY" />     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Texto completo formato PDF </font></p>     <p align="justify" class="Estilo4 Estilo15"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><strong>REFERENCIAS</strong></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">1. Garrity GM, Winters M, Searles DB. Taxonomic outline of the procaryotic genera. 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