<?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>1025-0255</journal-id>
<journal-title><![CDATA[Revista Archivo Médico de Camagüey]]></journal-title>
<abbrev-journal-title><![CDATA[AMC]]></abbrev-journal-title>
<issn>1025-0255</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de Camagüey]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1025-02552016000400014</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Efecto inmunomodulador anti-inflamatorio de la moxifloxacina como coadyuvante en la terapia periodontal]]></article-title>
<article-title xml:lang="en"><![CDATA[Immunomodulatory anti-inflammatory effect of moxifloxacin as an adjunct in periodontal therapy]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ardila Medina]]></surname>
<given-names><![CDATA[Carlos Martín]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bedoya García]]></surname>
<given-names><![CDATA[Jader]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Patiño Giraldo]]></surname>
<given-names><![CDATA[Jorge Eliecer]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad de Antioquia  ]]></institution>
<addr-line><![CDATA[Antioquia ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad de Chile  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Chile</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Universidad Antonio Nariño. Universidad de Antioquia  ]]></institution>
<addr-line><![CDATA[Antioquia ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>20</volume>
<numero>4</numero>
<fpage>444</fpage>
<lpage>451</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1025-02552016000400014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1025-02552016000400014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1025-02552016000400014&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Fundamento: la periodontitis es una enfermedad infecciosa que se presenta como producto de la interacción entre algunos microorganismos y diversas reacciones del huésped a la infección. La función inmunomodulatoria anti-inflamatoria de antimicrobianos como la moxifloxacina puede ser una cualidad de gran utilidad en el tratamiento de la periodontitis. Objetivo: revisar la literatura científica con el fin de determinar si la moxifloxacina presenta un efecto inmunomodulador. Métodos: se realizó una revisión sistemática de investigaciones realizadas en humanos o células humanas publicadas en las bases de datos Medline-Pubmed, SciELO, LILACS y Google académico entre 1996 y 2015, se utilizaron los siguientes términos en diferentes combinaciones: moxifloxacin, immunomodulation, cytokines, interleukines y tumor necrosisfactor. Se excluyeron las series de casos, resultados duplicados debido a las combinaciones de los términos de búsqueda, datos no disponibles, cartas al editor y revisiones históricas. Desarrollo: un total de nueve estudios presentaron disminución de la liberación de las interleuquinas1&#946;, 6, 8 mientras que cinco estudios mostraron su inhibición. Tres publicaciones demostraron inhibición del factor de necrosis tumoral &#945; y tres presentaron reducción de su liberación. Conclusiones: la moxifloxacina, además de su eficacia contra los principales periodontopatógenos, tiene un efecto inmunomodulador importante en el proceso inflamatorio de la periodontitis que debe tenerse en cuenta en la toma de decisiones clínicas para el tratamiento de esta enfermedad.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Background: periodontitis is an infectious disease that occurs as a result of the interaction between microorganisms and some different reactions of the host to infection. The anti-inflammatory immunomodulatory function of antimicrobial drugs such as moxifloxacin can be a useful quality in the treatment of periodontitis. Objective: to review the scientific literature related to the immunomodulatory effect of moxifloxacin. Methods: a systematic review of research conducted in humans or human cells published in Medline-Pubmed, SciELO, LILACS and academic Google between 1996 and 2015 data was performed using the following terms in different combinations: moxifloxacin, immunomodulation, cytokines, interleukins and tumor necrosis factor. Case series, duplicate results due to combinations of search terms, missing data, letters to the editor and historical revisions, were excluded. Development: a total of nine studies showed decreased release of the interleukins 1&#946;, 6, 8, while five studies showed inhibition. Similarly, three publications showed inhibition of tumor necrosis factor &#945; and three arranged reduction of their release. Conclusions: moxifloxacin, besides its effectiveness against the main periodontopathogens, has a significant immunomodulatory effect in the inflammatory process of periodontitis to be taken into account in the clinical decision to treat this disease.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[PERIODONTITIS]]></kwd>
<kwd lng="es"><![CDATA[INMUNOMODULACIÓN]]></kwd>
<kwd lng="es"><![CDATA[ANTIINFECCIOSOS]]></kwd>
<kwd lng="es"><![CDATA[ENFERMEDADES TRANSMISIBLES]]></kwd>
<kwd lng="es"><![CDATA[LITERATURA DE REVISIÓN COMO ASUNTO]]></kwd>
<kwd lng="en"><![CDATA[PERIODONTITIS]]></kwd>
<kwd lng="en"><![CDATA[IMMUNOMODULATION]]></kwd>
<kwd lng="en"><![CDATA[ANTI-INFECTIVE AGENTS]]></kwd>
<kwd lng="en"><![CDATA[COMMUNICABLE DISEASES]]></kwd>
<kwd lng="en"><![CDATA[REVIEW LITERATURE AS TOPIC]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>ARTICULOS DE REVISI&Oacute;N</b></font></p>     <p align="right">&nbsp;</p>     <p align="justify"><font size="4" face="Verdana, Arial, Helvetica, sans-serif"><b>Efecto inmunomodulador anti-inflamatorio de la  moxifloxacina como coadyuvante en la terapia periodontal</b></font></p>     <p align="justify">&nbsp;</p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="3" face="Verdana, Arial, Helvetica, sans-serif"><b><i>Immunomodulatory anti-inflammatory effect of  moxifloxacin as an adjunct in periodontal therapy</i></b></font></p>     <p align="justify">&nbsp;</p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>Dr.  C. Carlos Mart&iacute;n Ardila Medina </b><sup><b>I</b></sup><b>; Dr. Jader Bedoya Garc&iacute;a </b><sup><b>II</b></sup><b>;  Dr. Jorge Eliecer Pati&ntilde;o Giraldo </b><sup><b>III</b></sup></font></p>     <p align="justify">&nbsp;</p>     ]]></body>
<body><![CDATA[<p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">I Universidad de Antioquia. Antioquia, Colombia.    <br>   II Universidad de Chile. Chile.    <br>   III Universidad Antonio Nari&ntilde;o. Universidad de  Antioquia. Antioquia, Colombia.</font></p>     <p align="justify">&nbsp;</p>     <p align="justify">&nbsp;</p> <hr>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>RESUMEN</b></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>Fundamento: </b>la periodontitis es una  enfermedad infecciosa que se presenta como producto de la interacci&oacute;n entre  algunos microorganismos y diversas reacciones del hu&eacute;sped a la infecci&oacute;n. La funci&oacute;n  inmunomodulatoria anti-inflamatoria de antimicrobianos como la moxifloxacina  puede ser una cualidad de gran utilidad en el tratamiento de la periodontitis.    <br> </font><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>Objetivo:</b> revisar la  literatura cient&iacute;fica con el fin de determinar si la moxifloxacina  presenta un efecto inmunomodulador.    <br> </font><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>M&eacute;todos: </b>se realiz&oacute; una revisi&oacute;n sistem&aacute;tica de  investigaciones realizadas en humanos o c&eacute;lulas humanas publicadas en las bases de datos Medline-Pubmed, SciELO,  LILACS y Google acad&eacute;mico entre 1996 y 2015, se utilizaron los siguientes  t&eacute;rminos en diferentes combinaciones: moxifloxacin, immunomodulation,  cytokines, interleukines y tumor necrosisfactor. Se excluyeron las series de casos, resultados duplicados debido a  las combinaciones de los t&eacute;rminos de b&uacute;squeda, datos no disponibles, cartas al  editor y revisiones hist&oacute;ricas.    <br>   <b>Desarrollo:</b> un total de nueve estudios presentaron disminuci&oacute;n de la liberaci&oacute;n de las  interleuquinas1&beta;, 6, 8  mientras que cinco estudios mostraron su inhibici&oacute;n. Tres publicaciones  demostraron inhibici&oacute;n del factor de necrosis tumoral &alpha; y tres presentaron  reducci&oacute;n de su liberaci&oacute;n.    ]]></body>
<body><![CDATA[<br> </font><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>Conclusiones: </b>la moxifloxacina, adem&aacute;s de  su eficacia contra los principales periodontopat&oacute;genos, tiene un efecto  inmunomodulador importante en el proceso inflamatorio de la periodontitis que  debe tenerse en cuenta en la toma de decisiones cl&iacute;nicas para el tratamiento de  esta enfermedad.</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>DeCS: </b>PERIODONTITIS/terapia;  INMUNOMODULACI&Oacute;N; ANTIINFECCIOSOS; ENFERMEDADES TRANSMISIBLES; LITERATURA DE  REVISI&Oacute;N COMO ASUNTO.</font></p> <hr>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>ABSTRACT</b></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>Background: </b>periodontitis is an  infectious disease that occurs as a result of the interaction between  microorganisms and some different reactions of the host to infection. The  anti-inflammatory immunomodulatory function of antimicrobial drugs such as  moxifloxacin can be a useful quality in the treatment of periodontitis.    <br>   <b>Objective:</b> to review the scientific literature related to the immunomodulatory effect of  moxifloxacin.    <br>   <b>Methods: </b>a systematic review of research conducted in  humans or human cells published in Medline-Pubmed, SciELO, LILACS and academic  Google between 1996 and 2015 data was performed using the following terms in  different combinations: moxifloxacin, immunomodulation, cytokines, interleukins  and tumor necrosis factor. Case series, duplicate results due to combinations  of search terms, missing data, letters to the editor and historical revisions,  were excluded.    <br>   <b>Development: </b>a total of nine studies  showed decreased release of the interleukins 1&beta;, 6, 8, while five studies showed inhibition.  Similarly, three publications showed inhibition of tumor necrosis factor &alpha; and  three arranged reduction of their release.    <br>   <b>Conclusions:</b> moxifloxacin,  besides its effectiveness against the main periodontopathogens, has a  significant immunomodulatory effect in the inflammatory process of  periodontitis to be taken into account in the clinical decision to treat this  disease.</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>DeCS:</b> PERIODONTITIS/therapy;  IMMUNOMODULATION; ANTI-INFECTIVE AGENTS; COMMUNICABLE DISEASES; REVIEW  LITERATURE AS TOPIC.</font></p> <hr>     <p align="justify">&nbsp;</p>     ]]></body>
<body><![CDATA[<p align="justify">&nbsp;</p>     <p align="justify"><font size="3" face="Verdana, Arial, Helvetica, sans-serif"><b>INTRODUCCI&Oacute;N</b></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La  periodontitis es una enfermedad infecciosa que se presenta como producto de la  interacci&oacute;n entre algunos microorganismos y diversas reacciones del hu&eacute;sped a  la infecci&oacute;n. <sup>1</sup> La comprensi&oacute;n del proceso inmunoinflamatorio permite  entender a su vez el mecanismo involucrado en la destrucci&oacute;n de los tejidos  periodontales, en donde un n&uacute;mero importante de mediadores biol&oacute;gicos est&aacute;  presente, donde se incluye una variedad de citoquinas producidas por diferentes  c&eacute;lulas. Las citoquinas regulan la adhesi&oacute;n de mol&eacute;culas sobre los  leucocitos y las c&eacute;lulas endoteliales, fundamental para que los leucocitos  abandonen el sistema vascular y se infiltren alrededor de los tejidos. <sup>2</sup> La  interleuquina (IL) <sup>1</sup> y el factor de necrosis tumoral (FNT), considerados  mediadores inflamatorios primarios, estimulan la producci&oacute;n de mediadores  secundarios como las citoquinas quimiot&aacute;cticas y las ciclooxigenasas que a su  vez producen prostaglandinas. Este complejo proceso conduce a la ampliaci&oacute;n de  la respuesta inflamatoria, a la inducci&oacute;n de enzimas que degradan el tejido  conectivo y a la reabsorci&oacute;n &oacute;sea. <sup>3</sup></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La terapia mec&aacute;nica periodontal se considera un abordaje exitoso en el tratamiento de los pacientes con  periodontitis, pero no establece los cambios microbiol&oacute;gicos necesarios para  que los resultados terap&eacute;uticos se mantengan a largo plazo. El tratamiento  antimicrobiano sist&eacute;mico como coadyuvante a la terapia mec&aacute;nica periodontal,  gana importancia en la medida que permite mejorar los par&aacute;metros cl&iacute;nicos y  microbiol&oacute;gicos periodontales. <sup>4</sup> Las alternativas antimicrobianas  adjuntas a la terapia mec&aacute;nica para el tratamiento de la periodontitis incluyen  varios antibi&oacute;ticos y combinaciones de ellos.</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La moxifloxacina (MOX), es una fluoroquinolona de amplio espectro con  efecto sobre bacterias Gram negativas y Gram positivas, aerobias y anaerobias,  con actividad mejorada en microorganismos resistentes a la penicilina. Esta  quinolona ha demostrado muy buena eficacia cl&iacute;nica y microbiol&oacute;gica en el tratamiento  de la periodontitis. <sup>5, 6</sup></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La funci&oacute;n inmunomodulatoria anti-inflamatoria  de antimicrobianos como la moxifloxacina (MOX) puede ser una cualidad de gran  utilidad en el tratamiento de la periodontitis. El objetivo del art&iacute;culo es  revisar la literatura cient&iacute;fica con el fin de determinar si la MOX presenta un efecto  inmunomodulador.</font></p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="3" face="Verdana, Arial, Helvetica, sans-serif"><b>M&Eacute;TODOS</b></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Se  realiz&oacute; una revisi&oacute;n sistem&aacute;tica que incluy&oacute; una b&uacute;squeda en todos los idiomas  de art&iacute;culos publicados, entre 1996 y 2015, en las bases de datos:  Medline-Pubmed, SciELO, LILACS y Google acad&eacute;mico se utilizaron los siguientes  t&eacute;rminos en diferentes combinaciones: moxifloxacin, antibiotics, immunomodulation, cytokines, interleukines y  tumor necrosis factor. Se emplearon estrategias  adicionales con el fin de encontrar art&iacute;culos relevantes, se utilizaron  art&iacute;culos relacionados con el tema en la base de datos Medline-Pubmed,  a partir de las publicaciones que se encontraron en un inicio con los t&eacute;rminos  de b&uacute;squeda utilizados.</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Se incluyeron aquellos  art&iacute;culos que involucraron estudios realizados en seres humanos o en c&eacute;lulas  humanas. Se excluyeron las series de casos, resultados duplicados debido a las combinaciones de  los t&eacute;rminos de b&uacute;squeda, datos no disponibles, cartas al editor y revisiones  hist&oacute;ricas. De esta manera, se revisaron los textos  completos de las publicaciones seleccionadas.</font></p>     ]]></body>
<body><![CDATA[<p align="justify">&nbsp;</p>     <p align="justify"><font size="3" face="Verdana, Arial, Helvetica, sans-serif"><b>DESARROLLO</b></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La  b&uacute;squeda inicial de la revisi&oacute;n sistem&aacute;tica arroj&oacute; 32 publicaciones de las  cuales se excluyeron 10 debido a que no cumplieron los criterios establecidos  para su revisi&oacute;n. De esta forma, 22 art&iacute;culos potenciales fueron seleccionados  para la evaluaci&oacute;n del texto completo; sin embargo, seis de ellos no cumplieron  algunos criterios de inclusi&oacute;n, por lo que quedaron solo 16 publicaciones  relevantes para esta revisi&oacute;n (<a href="#figura1">figura 1</a>).</font></p>     <p align="justify">&nbsp;</p>     <p align="center"><img src="/img/revistas/amc/v20n4/f01140416.jpg" alt="figura 1" width="459" height="469" longdesc="../img/f01140416.jpg"><a name="figura1"></a></p>     
<p align="justify">&nbsp;</p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Los hallazgos m&aacute;s relevantes de los  estudios que cumplieron los criterios de selecci&oacute;n fueron: la mayor&iacute;a se  realizaron entre 2002 y 2015, catorce estudios fueron experimentales fase cero  y dos experimentales fase III, los monocitos fueron las c&eacute;lulas experimentales  m&aacute;s estudiadas; de igual forma, las IL 1&beta;, <sup>7-10</sup> 6, <sup>11-14</sup> 8 <sup>15-18</sup>  y el FNT &alpha; <sup>19-22</sup> son los mediadores inflamatorios  m&aacute;s investigados. Un total de nueve estudios presentaron disminuci&oacute;n de la liberaci&oacute;n  de estas IL, mientras que cinco estudios mostraron su inhibici&oacute;n Se encontr&oacute;  que tres publicaciones demostraron inhibici&oacute;n del FNT&alpha; <sup>17, 19, 20 </sup> y tres  desplegaron reducci&oacute;n de su liberaci&oacute;n. <sup>9, 10, 13 </sup> Solo una  investigaci&oacute;n no report&oacute; cambios en la liberaci&oacute;n de los mediadores, <sup>21</sup>  mientras que solo un estudio investig&oacute; la   IL 10 y el interfer&oacute;n &gamma;,  donde se observ&oacute; disminuci&oacute;n de los dos mediadores (<a href="#tabla1">tabla 1</a>). <sup>22</sup></font></p>     <p align="justify">&nbsp;</p>     <p align="center"><img src="/img/revistas/amc/v20n4/t01140416.jpg" alt="tabla 1" width="584" height="503" longdesc="../img/t01140416.jpg"><a name="tabla1"></a></p>     
<p align="justify">&nbsp;</p>     ]]></body>
<body><![CDATA[<p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La mayor&iacute;a de los estudios excluidos  se descartaron por no estudiar los mediadores de inter&eacute;s <sup>23-26</sup> o por  tratarse de una revisi&oacute;n de tema <sup>27</sup> o reporte de caso (<a href="#tabla2">tabla 2</a>). <sup>28</sup></font></p>     <p align="justify">&nbsp;</p>     <p align="center"><img src="/img/revistas/amc/v20n4/t02140416.jpg" alt="tabla 2" width="562" height="207" longdesc="../img/t02140416.jpg"><a name="tabla2"></a></p>     
<p align="justify">&nbsp;</p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La  terapia antimicrobiana sist&eacute;mica como coadyuvante a la terapia mec&aacute;nica  periodontal presenta gran eficacia debido a que permite mejorar los par&aacute;metros  cl&iacute;nicos (nivel de inserci&oacute;n cl&iacute;nica, profundidad al sondaje) y microbiol&oacute;gicos  (eliminaci&oacute;n o reducci&oacute;n de la cantidad de microorganismos. <sup>29, 30 </sup>  Las alternativas antimicrobianas adjuntas a la terapia mec&aacute;nica para el  tratamiento de las periodontitis incluyen varios antibi&oacute;ticos y combinaciones  de ellos. Adem&aacute;s, del efecto bactericida y bacteriost&aacute;tico de los  antimicrobianos sobre los periodontopat&oacute;genos, es importante examinar su efecto  inmunomodulador y su posible relaci&oacute;n con el componente inmune de la  periodontitis.</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">El  efecto inmunomodulador de varios antimicrobianos se ha estudiado en varias  &aacute;reas m&eacute;dicas, <sup>8</sup> por lo cual emerge la posibilidad de documentar un  efecto terap&eacute;utico inmunomodulador adicional al efecto antibacteriano en el  manejo periodontal. La doxiciclina sist&eacute;mica a pesar de mostrar un efecto  inmunomodulador importante <sup>7</sup> presenta resultados limitados desde el  punto de vista microbiol&oacute;gico al no reducir los niveles de <i>treponema denticola</i> y <i>aggregatibacter  actinomycetemcomitans</i>, <sup>31</sup> periodontopat&oacute;genos de gran relevancia  en la etiopatogenia de las enfermedades periodontales.</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La  azitromicina tiene efecto inhibidor sobre la IL 8 <sup>7</sup> pero algunos investigadores no  han observado eficacia sobre la flora subgingival, <sup>32</sup> y comparado  con la terapia mec&aacute;nica sola, no muestra diferencias significativas en su  eficacia microbiol&oacute;gica. <sup>33</sup> No se conocen estudios, desde el punto de  vista de inhibici&oacute;n de citoquinas, que investiguen el efecto inmunomodulador de  la combinaci&oacute;n amoxicilina m&aacute;s metronidazol, protocolo usado con amplitud en el  tratamiento coadyuvante de la periodontitis, <sup>34</sup> sin embargo, los  betalact&aacute;micos se asocian con el aumento de IL 1&beta; y 6. <sup>7</sup> Por otra  parte, investigaciones concernientes a las quinolonas muestran un efecto  inmunomodulador potente; <sup>26</sup> la ciprofloxacina con un efecto menos  selectivo sobre las IL 6 y 8 <sup>18</sup> muestra baja actividad sobre  microorganismos anaerobios Gram negativos, <sup>11</sup> mientras que la MOX con eficacia cl&iacute;nica y  microbiol&oacute;gica sobre periodontopat&oacute;genos, <sup>5</sup> presenta un efecto  supresor e inhibidor en la liberaci&oacute;n de mediadores como las IL 1&beta;, 7-10 6, <sup>11-14</sup> 8 <sup>15-18</sup>  y el FNT &alpha;. <sup>19-22</sup></font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Otro aspecto importante,  es que el efecto de la MOX  sobre la liberaci&oacute;n de las mol&eacute;culas inflamatorias es dependiente de la dosis,  es decir, al aumentar la dosis su efecto supresor e inhibidor es mayor, <sup>9, 13, 19 </sup> caracter&iacute;stica fundamental que se debe tener en cuenta durante su  manejo cl&iacute;nico.</font></p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="3" face="Verdana, Arial, Helvetica, sans-serif"><b>CONCLUSIONES</b></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">La principal conclusi&oacute;n de esta  revisi&oacute;n es que la moxifloxacina, adem&aacute;s de su eficacia contra los principales periodontopat&oacute;genos,  tiene un efecto inmunomodulador importante en el proceso inflamatorio de la  periodontitis que debe tenerse en cuenta en la toma de decisiones cl&iacute;nicas para  el tratamiento de esta enfermedad.</font></p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="3" face="Verdana, Arial, Helvetica, sans-serif"><b>REFERENCIAS BIBLIOGR&Aacute;FICAS</b></font></p>     <!-- ref --><p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">1. Olsen I. From the Acta Prize Lecture 2014: the periodontal-systemic connection seen from a microbiological standpoint. 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J Dent. 2012 Jul;40(7):556-63.    </font></p>     <!-- ref --><p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">33. Sampaio E, Rocha M, Figueiredo LC, Faveri M, Duarte PM, Gomes Lira EA, et al. Clinical and microbiological effects of azithromycin in the treatment of generalized chronic periodontitis: A randomized placebo-controlled clinical trial. J Clin Periodontol. 2011 Sep;38(9):838-46.    </font></p>     <!-- ref --><p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">34. Keestra JA, Grosjean I, Coucke W, Quirynen M, Teughels W. Non-surgical periodontal therapy with systemic antibiotics in patients with untreated aggressive periodontitis: a systematic review and meta-analysis. J Periodontal Res. 2015 Dec;50(6):689-706.    </font></p>     <p align="justify">&nbsp;</p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Recibido: 6 de abril de 2016</font></p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Aprobado: 30 de mayo de 2016</font></p>     <p align="justify">&nbsp;</p>     <p align="justify">&nbsp;</p>     <p align="justify"><font size="2" face="Verdana, Arial, Helvetica, sans-serif">Dr.  C. Carlos Mart&iacute;n Ardila Medina. Doctor en Epidemiolog&iacute;a. Profesor Titular. Universidad de  Antioquia. Antioquia, Colombia.</font></p>      ]]></body><back>
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