<?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>1413-8670</journal-id>
<journal-title><![CDATA[Brazilian Journal of Infectious Diseases]]></journal-title>
<abbrev-journal-title><![CDATA[Braz J Infect Dis]]></abbrev-journal-title>
<issn>1413-8670</issn>
<publisher>
<publisher-name><![CDATA[Brazilian Society of Infectious Diseases]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1413-86702004000200003</article-id>
<article-id pub-id-type="doi">10.1590/S1413-86702004000200003</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Seroprevalence of hepatitis B and C in the Western Brazilian Amazon region (Rio Branco, Acre): a pilot study carried out during a hepatitis B vaccination program]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tavares-Neto]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Almeida]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Soares]]></surname>
<given-names><![CDATA[M. C.]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Uchoa]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Viana]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Darub]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Farias]]></surname>
<given-names><![CDATA[E.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rocha]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vitvitski]]></surname>
<given-names><![CDATA[L.]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Paraná]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,University of Bahia Group for the Study of Viral Hepatitis ]]></institution>
<addr-line><![CDATA[Salvador BA]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Acre State Public Health Program  ]]></institution>
<addr-line><![CDATA[Rio Branco AC]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Evandro Chagas Institute  ]]></institution>
<addr-line><![CDATA[Belém PA]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="A04">
<institution><![CDATA[,Institut National de la Santé et de la Recherche Médicale  ]]></institution>
<addr-line><![CDATA[Lyon ]]></addr-line>
<country>France</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>04</month>
<year>2004</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>04</month>
<year>2004</year>
</pub-date>
<volume>8</volume>
<numero>2</numero>
<fpage>133</fpage>
<lpage>139</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S1413-86702004000200003&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.br/scielo.php?script=sci_abstract&amp;pid=S1413-86702004000200003&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.br/scielo.php?script=sci_pdf&amp;pid=S1413-86702004000200003&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[In 1999, on the occasion of the application of the first vaccine dose during the state vaccination campaign against hepatitis B virus (HBV), 390 individuals from the town of Rio Branco, Acre, aged two or more years were selected for the determination of the seroprevalence of HBV and HCV. HBV markers (HBsAg, anti-HBs, and anti-HBc IgG) were determined on this occasion and anti-HBs antibodies were also assessed 30 days after the third vaccine dose. At the time of vaccination, 39% of the individuals were still susceptible to HBV, while 61% presented serologic evidence of previous HBV contact or previous vaccination. The individuals with previous HBV contact were significantly older (p<0.001) than those without HBV markers. Of the 192 individuals who returned for reexamination, 30 days after the third dose, 158 (82.3%) had received three vaccine doses, and only 60 (31.2%) belonged to the group without HBV markers. In these individuals, the seroconversion rate after the third dose was 92% (55/60). In conclusion, we found considerable HBV in this population, indicating the need for pursuing the immunization programs. We also found high rates of vaccination coverage in the Western Brazilian Amazon region.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Hepatitis B vaccination]]></kwd>
<kwd lng="en"><![CDATA[Amazonia]]></kwd>
<kwd lng="en"><![CDATA[hepatitis B]]></kwd>
<kwd lng="en"><![CDATA[hepatitis C]]></kwd>
<kwd lng="en"><![CDATA[epidemiology]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><font size="2" face="Verdana"><b>ORIGINAL PAPERS</b></font></p>     <p>&nbsp;</p>     <p><font size="4" face="Verdana"><B><a name="tx"></a>Seroprevalence of hepatitis    B and C in the Western Brazilian Amazon region (Rio Branco, Acre): a pilot study    carried out during a hepatitis B vaccination program </b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana"><B>J. Tavares-Neto<SUP>I, II</SUP>; D. Almeida<SUP>I</SUP>;    M. C. Soares<SUP>III</SUP>; R. Uchoa<sup>II</sup>; S. Viana<sup>II</sup>; R.    Darub<sup>II</sup>; E. Farias<sup>II</sup>; G. Rocha<sup>II</sup>; L. Vitvitski<sup>IV</sup>;    R. Paran&aacute;<sup>I</sup></b> </font></p>     <p><font size="2" face="Verdana"><sup>I</sup>Postgraduate Program, University    of Bahia, Brazil, Group for the Study of Viral Hepatitis, Salvador, BA<SUP>    <br>    II</sup>Acre State Public Health Program, Rio Branco, AC    <br>   <sup>III</sup>Evandro Chagas Institute, Bel&eacute;m, PA, Brazil    <br>   <sup>IV</sup>INSERM, 271 Unit, Lyon, France </font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"><a href="#end">Correspondence</a></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p> <hr size="1" noshade>     <p><font size="2" face="Verdana"><b>ABSTRACT</b></font></p>     <p><font size="2" face="Verdana">In 1999, on the occasion of the application of    the first vaccine dose during the state vaccination campaign against hepatitis    B virus (HBV), 390 individuals from the town of Rio Branco, Acre, aged two or    more years were selected for the determination of the seroprevalence of HBV    and HCV. HBV markers (HBsAg, anti-HBs, and anti-HBc IgG) were determined on    this occasion and anti-HBs antibodies were also assessed 30 days after the third    vaccine dose. At the time of vaccination, 39% of the individuals were still    susceptible to HBV, while 61% presented serologic evidence of previous HBV contact    or previous vaccination. The individuals with previous HBV contact were significantly    older (p&lt;0.001) than those without HBV markers. Of the 192 individuals who    returned for reexamination, 30 days after the third dose, 158 (82.3%) had received    three vaccine doses, and only 60 (31.2%) belonged to the group without HBV markers.    In these individuals, the seroconversion rate after the third dose was 92% (55/60).    In conclusion, we found considerable HBV in this population, indicating the    need for pursuing the immunization programs. We also found high rates of vaccination    coverage in the Western Brazilian Amazon region. </font></p>     <p><font size="2" face="Verdana"><b>Key words:</b> Hepatitis B vaccination, Amazonia,    hepatitis B, hepatitis C, epidemiology.</font></p> <hr size="1" noshade>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana">Hepatitis B is a worldwide public health problem,    especially in developing countries. Chronic infection after exposure to hepatitis    B virus (HBV) has been observed in 30% to 90% of children aged less than five    years. On the other hand, exposed adults become chronic carriers of HBV in only    2 to 5% of cases &#91;1&#93;. In the United States, it is estimated that 500,000 to    1,000,000 individuals are chronically infected with the B virus, and 15% to    25% of them will die prematurely due to liver disease or hepatocellular carcinoma    &#91;2&#93;. These aspects of the natural history of HBV have prompted the implementation    of vaccination programs against HBV in various countries worldwide &#91;3-5&#93;. </font></p>     <p><font size="2" face="Verdana"> In the Brazilian Amazon region, HBV infection    is a severe health problem, which is complicated by the presence of hepatitis    D virus (HDV) in the area. Fulminant hepatitis outbreaks due to HDV superinfection    of HBV carriers is still frequently observed in this region &#91;6&#93;. No recent seroepidemiologic    studies on HBV are available in the state of Acre, in the eastern Brazilian    Amazon region, although evidence obtained from hospital reports and blood donor    candidates indicates a high prevalence of individuals chronically infected with    HBV. Most of them are adolescents or young adults, though older adults commonly    suffer from acute hepatitis B. </font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"> Unfortunately, no population study concerning    the prevalence of HCV is available so far. The large number      of HCV carriers in our outpatient unit seen at the referral hospital of Rio    Branco (Acre) means that further prevalence studies are warranted. </font></p>     <p><font size="2" face="Verdana"> The first-generation plasma-derived vaccine    against the B virus was introduced in the 1970's &#91;7&#93;. In the 1980's, a recombinant    HBsAg vaccine was produced, which showed excellent tolerance and efficacy &#91;8-11&#93;.    </font></p>     <p><font size="2" face="Verdana"> In Brazil, the official immunization schedule    includes the HBV vaccine, only for newborns and children younger than 15 years.    Despite this recommendation, HBV vaccine coverage of newborns was less than    25% during the period from 1990 to 1998 in all 22 municipalities of the state    of Acre (DABS - SESSACRE, unpublished data). This situation led the government    of Acre, supported by the National Health Foundation and the National Immunization    Program (PNI, Ministry of Health), to organize a mass vaccination campaign against    HBV in 1996, which consisted of the application of three doses (at 0, 1 and    6 months). </font></p>     <p><font size="2" face="Verdana"> Taking advantage of this ambitious vaccination    program, we have studied serum HBV and HCV markers in a subset of vaccinated    individuals from the town of Rio Branco, Acre, obtained before application of    the first HBV vaccine dose and reexamined in part of the sample 30 days after    the third dose. </font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><B>Material and Methods</B> </font></p>     <p><font size="2" face="Verdana"> On the first day of the state vaccination campaign    against HBV, seven mobile teams (each consisting of a medical student and a    technician from the Central Public Health Laboratory of Acre) visited the 212    vaccination centers of the town of Rio Branco. Each team was responsible for    one of the two district areas of the municipality of Rio Branco, an urban area    with about 280,000 inhabitants. Rio Branco is the westernmost town among the    large cities of the Brazilian Amazon region (<a href="#fig01">Figure 1</a>).    </font></p>     <p><a name="fig01"></a></p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/bjid/v8n2/a03fig01.gif"></p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p><font size="2" face="Verdana"> Upon the arrival of the mobile team at a given    vaccination center, one or two individuals were selected for blood collection,    answered a questionnaire and gave written informed consent to participate in    the study. The first individual selected was the person in the vaccination line    who, upon arrival of the team, was seen by one of the volunteers ("vaccinator")    of the respective center who recorded the personal data of each patient. At    centers with more than 30 individuals per line, a second individual was selected,    who was the person following the first one, provided that no family relationship    existed between them. When one of these two persons refused to participate,    the following person in the vaccination line was included. All infants aged    less than 24 months were excluded due to difficulties in blood sample collection.    A total of 394 individuals aged 2 to 79 years were evaluated. </font></p>     <p><font size="2" face="Verdana"> The number of household dwellers and the number    of rooms in the dwelling were obtained from the individuals included in the    study (or their legally responsible guardian) as socioeconomic indicators. Patients    reporting more than two individuals per room were considered to belong to a    poor socioeconomic stratum, while two or fewer persons per room indicated a    good socioeconomic level. </font></p>     <p><font size="2" face="Verdana"> After filling out the questionnaire, 5 ml venous    blood was collected without anticoagulant. The blood samples were then centrifuged    and stored at -20ºC at the Central Public Network Laboratory until    they were sent to the Hepatitis Laboratory, Evandro Chagas Institute, Bel&eacute;m,    Brazil, for the determination of serologic markers of HBV (HBsAg, anti-HBs and    total anti-HBc IgG), HCV, and HDV. All markers were assayed using a commercial    enzyme immunoassay (Organon<SUP>®</SUP>, Abbott, Chicago, IL, for HBsAg    and anti-HDV; anti-HBs, anti-HBc IgG, and anti-HCV). </font></p>     <p><font size="2" face="Verdana"> The second phase of the study was carried out    one month after application of the third HBV vaccine dose between January 19    and January 21, 2000 (at this time, the serological results of the first serum    samples were still unknown). Eight days before the beginning of the second phase    all participants in the study (n=394) received a letter from the State Secretary    Office of Health and Sanitation (SESSACRE), inviting them for a new blood collection    for serological determination of anti-HBs markers. The reason for the study    was explained in simple language accessible to the lay public. One hundred ninety    two (49.2%) individuals accepted  the invitation    during the second phase and attended the Blood Center of Acre State (HEMOACRE).    The blood samples obtained were then processed as described above, and the second    module of the questionnaire was filled out. </font></p>     <p><font size="2" face="Verdana"> The vaccine used during the state vaccination    campaign against HBV was Engerix<SUP>®</SUP> B (SmithKline Beecham). The    vaccine dose used was 10 <font face="Symbol">m</font>g for children aged 2 to    10 years and 20 <font face="Symbol">m</font>g for individuals 11 years or older.    </font></p>     <p><font size="2" face="Verdana"> Statistical analysis was carried out using the    Statistical Package for the Social Sciences (SPSS) software. Natives from the    state of Acre and individuals born in the municipalities of the eastern region    of the state were recorded as being from the Vale do Rio Branco region, while    those born in municipalities of the central and western region were considered    to be from Vale do Rio Juru&aacute;. The mean, standard deviation and median    were determined for continuous variables, while frequencies were assessed for    categorical variables. The student's t test was used to analyse continuous variables    and the <I>X</I><SUP>2</SUP> test was performed to analyse categorical variables.    The associations were considered to be statistically significant at an a error    probability of <u>&lt;</u>0.05 (<u>&lt;</u>5%). </font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><B>Results</B> </font></p>     <p><font size="2" face="Verdana"><I>First phase of the study</I>  </font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"> Of the 394 individuals selected, four were excluded    because of insufficient serum samples. The gender proportion was similar in    this population (n=390; male: 48.2% <I>vs.</I> female: 51.2%), and mean age    was 26.5 &plusmn; 14.9 years (median of 23 and mode of 13 years), range 2 to    79 years. The distribution of individuals according to positivity for the HBV    serologic markers studied was as follows: 3.3% (n=13) were positive for HbsAg    and 34.3% (n=134) for anti-HBs and anti-HBc IgG. Anti-HBc IgG alone was detected    in 13 (3.3%) individuals. Anti-HBs alone (previous vaccination) were observed    in 14.1% (n=55) of the individuals. Only 39.0% (n=152) of the population studied    was seronegative for all three HBV serologic markers (HBsAg, anti-HBc and anti-HBs).    <a href="#tab01">Table I</a> shows the distribution of the serologic groups,    i.e., previously vaccinated, previous HBV exposure, and two patients with HDV    co-infection. </font></p>     <p><a name="tab01"></a></p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/bjid/v8n2/a03tab01.gif"></p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana"> Of 386 (99.0%) individuals studied, 16 (4.2%)    were positive for anti-HCV, but no confirmatory test was applied.<a href="#tab01">Table    1</a> also shows the demographic characteristics of the sample, with a similar    gender distribution (p&gt;0.48) being observed for each serological group. Mean    age was significantly higher in the HBsAg-positive group (35.7 &plusmn; 13.2    years) and in the group with HBV exposure. (36.7 &plusmn; 14.1 years; p&lt;0.03    and p&lt;0.001, respectively) and was significantly lower in the groups of previously    vaccinated individuals (15.4 &plusmn; 9.9 years) and individuals without HBV    markers (21.9 &plusmn; 11.2 years; p&lt;0.0001). </font></p>     <p><font size="2" face="Verdana"> Race distribution (whites = 183, non-whites    = 207; p&gt;0.59) and origin (born in the state of Acre <I>vs.</I> born in other    states; p&gt;0.39) were similar among the serological groups. When individuals    from the state of Acre (n=316, 81.0%) were analyzed according to the region    of the municipality where they were born (Vale do Rio Acre or Vale do Rio Juru&aacute;),    individuals from the towns of Vale do Rio Juru&aacute; were significantly more    frequent in the group with a past infection (p&lt;0.001) and less frequent in    the group of vaccinated (p&lt;0.001) or susceptible individuals (p&lt;0.006).    </font></p>     <p><font size="2" face="Verdana"> A strong association with previous immunization    (p&lt;0.001) was observed in individuals positive for anti-HBs, without anti-HBc    IgG (p&lt;0.001, <a href="#tab01">Table 1</a>). However, a similar distribution    of the vaccination history was observed for HbsAg-positive individuals (p&gt;0.20),    and in those with a past and resolved infection (p=0.69). The history of jaundice    was similar for the serological groups studied (HBsAg, p&gt;0.08; anti-HBs positive    with and without anti-HBc IgG, p&gt;0.70; individuals without HBV markers, p&gt;0.70).    </font></p>     <p><font size="2" face="Verdana"> In the analysis of the distribution of individuals    according to the number of rooms in the dwelling, most of them (64.9%, 253/390)    belonged to the stratum of <u>&lt;</u>2 persons/room, while the distribution    of those with more than two persons/room was similar for the serological groups.    </font></p>     <p><font size="2" face="Verdana"><I>Second phase of the study </I> </font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"> Only 192 (49.2%) of the 394 invited individuals    participated in the second phase of the study, with return of the letters to    the sender (SESSACRE). The main reason (108/198, 54.5%) for the lack of participation    was related to mail and address changes. </font></p>     <p><font size="2" face="Verdana"> Among the 192 individuals analyzed, 158 (82.3%)    reported the use of three HBV vaccine doses, 28 (14.6%) received two doses and    6 (3.1%) only one dose on the occasion of the state vaccination campaign against    HBV. Forty-five (23.4%) of them were previously immune (anti-HBs positive, detected    on the occasion of the administration of the first vaccine dose), 8 (4.2%) were    HBV carriers (HbsAg positive), and 79 (41.2%) presented a serology compatible    with a past and resolved HBV infection, i.e., only 60 (31.2%) individuals were    still susceptible to HBV (HBsAg, anti-HBs and anti-HBc negative). </font></p>     <p><font size="2" face="Verdana"> Among the 60 individuals susceptible to HBV,    most (n=50, 83%) received three vaccine doses, 7 (12%) received two doses, and    3 (5%) only one dose, with the anti-HBs seroconversion rate (serum sample obtained    30 days after the third vaccine dose) being 92% (46/50), 100% (7/7) and 67%    (2/3), respectively. </font></p>     <p><font size="2" face="Verdana"> Of the 5 (8%) non-seroconverted cases (anti-HBs    negative 30 days after the third vaccine dose), one had received only one dose    and four had received three doses. </font></p>     <p><font size="2" face="Verdana"> At the end of the study, the results of the    serological tests (including those positive for anti-HCV) were sent to the 390    individuals by regular mail. When appropriate, the person was advised to attend    the Service of Infectious and Parasitic Diseases of the General Hospital of    Rio Branco. Community health agents from the area in question tried to identify    cases of previously returned correspondence (n=108) or those returned on the    second occasion (n=41), and were able to locate 136 (91.3%) individuals. </font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><B>Discussion</B> </font></p>     <p><font size="2" face="Verdana"> Second-generation vaccines using recombinant    viral protein have provided efficient prophylaxis against HBV, but despite these    efforts about 350 million people are estimated to be infected with the virus,    rendering HBV an important carcinogen &#91;12&#93;. Nevertheless, vaccines and other    control measures have led to a decline in the prevalence of HBV over the last    few years, although HBV infection continues to be a severe public health problem    worldwide, with some regions such as Asia, the east coast of Africa and the    Amazon region being hyperendemic &#91;13&#93;. Especially in this region of Latin America,    vaccination against HBV can also lead to an associated decline in the prevalence    of HDV. </font></p>     <p><font size="2" face="Verdana">In this population, although vaccination of children    younger than 15 years, including newborns, has been encouraged by health authorities,    only 25.4% of the   individuals reported    previous vaccination against HBV, a rate similar to the vaccination frequencies    reported for the 22 municipalities of the state of Acre during the period from    1990 to 1998 (DABS - SESSACRE, unpublished data). </font></p>     <p><font size="2" face="Verdana"> The number of cases in the state of Acre with    chronic viral hepatitis or cirrhosis, including patients younger than 25 years    and individuals transferred for treatment outside the home (DCA - SESSACRE,    unpublished data), demonstrates the relevance of HBV as a health problem, and    also explains the great mobilization of the population on the days of state    vaccination, as well as the high rates (&gt;82%) of vaccination coverage reached    on the days of the state campaign (DABS/PNI - SESSACRE, unpublished data). </font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"> As an example of the relevance of HBV infection    in the state of Acre, even though acute hepatitis B caused jaundice in only    one-third of the cases &#91;14&#93;, a history of hepatitis was reported by 15.7% of    the individuals studied. In contrast, a large part of the population tested    positive for HBsAg (3.3%) or for HBV serologic markers compatible with past    exposure. Another group of individuals (20.8%) presented isolated anti-HBs compatible    with a history of vaccination, a frequency similar to that observed for individuals    who reported previous vaccination (25.4%). Only 39.0% of the vaccinated individuals    were still susceptible to HBV infection (HBsAg, anti-HBs and anti-HBc negative)    and thus benefitted from the vaccination program. Therefore, it is important    that in this region vaccination against HBV is preceded by serum anti-HBs determination    in isolated cases or in small population groups, an unfeasible and expensive    step when applied to vaccination programs similar to that carried out in the    state of Acre. </font></p>     <p><font size="2" face="Verdana"> In addition, the rejection rate of blood donor    candidates due to anti-HBc seropositivity has been found to be abnormally high    in the Amazon region when compared to other regions of the country &#91;15&#93;. This    is further demonstrated by the previous observation that 36.9% of individuals    presented HBV markers. </font></p>     <p><font size="2" face="Verdana"> Recently, further concern has been raised regarding    the high prevalence of anti-HCV among blood donor candidates in this region.    This fact, together with the exclusion of blood donors due to anti-HBc IgG seropositivity,    has generated a serious shortage of blood in the region. </font></p>     <p><font size="2" face="Verdana"> Despite the pilot study character of the present    investigation, these indicators, in addition to the high prevalence of anti-HCV    (4.2%) and anti-HDV (0.5%), demonstrate the relevance of hepatotropic viral    infections in this region of the country &#91;6&#93; and should thus encourage further    action by government and research institutions. </font></p>     <p><font size="2" face="Verdana"> Unfortunately, no confirmatory test was performed    in order to validate ELISA anti-HCV-positive cases. Nevertheless, we found a    high prevalence of anti-HCV in this population, which seems to be very close    to the actual prevalence of HCV in blood donor candidates from the state of    Acre. In addition, the serum samples were handled under appropriate conditions    and stored at -20ºC, as soon as collected. </font></p>     <p><font size="2" face="Verdana"> Although associated with or influenced by multiple    biological, social and economic factors in Brazil, gender and race distribution    was similar among the four serological groups, further supporting the assumption    of homogeneity of the sample and the wide dissemination of HBV in the population,    irrespective of other social and biological characteristics. In this respect,    the similarity between the serological groups in the proportion of individuals    living in dwellings with more than two persons/room also demonstrates that the    circulation of HBV in the population from Rio Branco town seems to be independent    of socioeconomic level. </font></p>     <p><font size="2" face="Verdana"> No difference was observed between individuals    born in the state of Acre and those from other states of the country, although    this type of association is affected by multiple variables, including the time    of residence in the Amazon region or, more specifically, in the state of Acre.    </font></p>     <p><font size="2" face="Verdana"> The impact of HBV infection has been known to    be more relevant among residents in the Vale do Rio Juru&aacute; municipality    (DABS - SESSACRE and HEMOACRE, unpublished data), in agreement with the significantly    higher frequency (67.8%, p&lt;0.001) of anti-HBc-positive cases among individuals    from this area. </font></p>     <p><font size="2" face="Verdana"> The high frequency (82.3%) of individuals receiving    three vaccine doses among those reassessed 30 days      after the third dose demonstrates good compliance of the population with the    state vaccination campaign. </font></p>     <p><font size="2" face="Verdana"> Although one may speculate about the large number    of individuals who did not respond to the call during the second phase, this    apparently did not cause distortions in the results, since a similar distribution    of the variables was observed for individuals who participated in the second    phase of the study (n=192) and those studied during the first phase (n=390).    The few non-seroconverted cases (n=5), especially the four individuals who received    three vaccine doses, might be explained by factors associated with vaccine application,    the vaccine itself or host characteristics &#91;16,17&#93;. </font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"> In conclusion, evidence of the strong impact    of HBV on public health demonstrates that a similar vaccination program could    be applied in places with characteristics similar to those of Acre state, where    large, geographically isolated areas prevent the implementation of various public    programs or services.  This study also demonstrated    that HCV infection is an important problem in the Brazilian Amazon region, which    requires further studies and greater attention on the part of federal government    health authorities. </font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><B>Acknowledgments</B> </font></p>     <p><font size="2" face="Verdana"> We thank the medical students of Acre and the    students of the Medical School of Cuba, as well as Master's student Jailson    de Ara&uacute;jo Silva (UFBA) and the students Juliano Freitas-Andrade (UFBA),    Ciro Falc&atilde;o Macedo Jr. (UNI - RJ), and Thiago Neves Paiva (UBM - RP,    SP). This study was supported by SESSACRE (Government of Acre), CNPq, and the    CAPES/COFECUB 404/02 project as part of the French/Brazilian Study Group on    Viral Hepatitis. </font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><B>References</B> </font></p>     <!-- ref --><p><font size="2" face="Verdana"> 1. Walsh K., Alexander G.J. Update on chronic    viral hepatitis. Postgrad Med J <B>2001</B>;77:498-505. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000079&pid=S1413-8670200400020000300001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 2. Holmes-Mc Nary M. Impact factors on development    of cirrhosis and subsequent hepatocellular carcinoma. Compend Contin Educ Dent    <B>2001</B>;22,19-33. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000080&pid=S1413-8670200400020000300002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 3. Hsu H., Chen D., Chuang C., et al. Efficacy    of a mass hepatitis B vaccination program in Taiwan. Studies on 3464 infants    of hepatitis B surface antigen-carrier mothers. JAMA <B>1988</B>;260:2231-5.    </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000081&pid=S1413-8670200400020000300003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 4. Goh K., Doraisingham S., Tan K., et al. The    hepatitis B immunization programme in Singapore. Bulletin of the World Health    Organization <B>1989</B>;67:65-70. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000082&pid=S1413-8670200400020000300004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 5. Jilg W. Preventive vaccination for viral    hepatitis. Zeitschrift f&uuml;r Gastroenterologie <B>1997</B>;35:585-90. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000083&pid=S1413-8670200400020000300005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 6. Souto F., Fontes C., Oliveira J., et al.    Epidemiological survey of infection with hepatitis B virus in the savanna and    wetlands (Pantanal) of central Brazil. Annals of Tropical Medicine and Parasitology    <B>1997</B>;91:411-6. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000084&pid=S1413-8670200400020000300006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 7. Van Herck K., Van Damme P., Collard F., Thoelen    S. Two-dose combined vaccination against hepatitis A and B in healthy subjects    aged 11-18 years. Scandinavian Journal of Gastroenterology <B>1999</B>;34:1236-40.    </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000085&pid=S1413-8670200400020000300007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 8. Emini E.A., Ellis R.W., Miller W.J., et al.    Production and immunological analysis of recombinant hepatitis B vaccine. Journal    of Infection <B>1986</B>;13(Suppl. A):3-9. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000086&pid=S1413-8670200400020000300008&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana"> 9. Zajac B.A., West D.J., McAleer W.J., Scolnick    E.M. Overview of clinical studies with hepatitis vaccine made by recombinant    DNA. Journal of Infection <B>1986</B>;13(Suppl. A):36-45. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000087&pid=S1413-8670200400020000300009&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">10. Jilg W., Schmidt M., Deinhardt F. Vaccination    against hepatitis B: Comparison of three different vaccination schedules. The    Journal of Infectious Diseases <B>1989</B>;160,766-9. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000088&pid=S1413-8670200400020000300010&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">11. Hadler S.C., de Monzon M.A., Lugo D.R., Perez    M. Effect of timing of hepatitis B vaccine doses on response to vaccine in Yucpa    Indians. Vaccine <B>1989</B>;7:106-10. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000089&pid=S1413-8670200400020000300011&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">12. Chen C.J., You S.L., Lin L.H., et al. Cancer    epidemiology and control in Taiwan: a brief review. Jpn J Clin Oncol <B>2002</B>;32    (Suppl S):66-81. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000090&pid=S1413-8670200400020000300012&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">13. Bensabath G., Hadler S.C., Soares M.C., et    al. Hepatitis delta virus infection and Labrea hepatitis. Prevalence and role    in fulminant hepatitis in the Amazon Basin. JAMA <B>1987</B>;258,479-83. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000091&pid=S1413-8670200400020000300013&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">15. Souto F., Fontes C., Gaspar A., et al. Concomitant    high prevalence of hepatitis C virus antibody and hepatitis B viral markers    in a small village of the Amazon region in Mato Grosso State, Brazil. Revista    do Instituto de Medicina Tropical de S&atilde;o Paulo <B>1996</B>;38,221-3.    </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000092&pid=S1413-8670200400020000300014&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">16. Liu P., Xu H., Wang X., et al. Field epidemiological    and experimental study on relationship between genetic factor and nonresponse    or hyporesponse to hepatitis B vaccine. Chin Med J <B>2000</B>;113,547-50. </font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000093&pid=S1413-8670200400020000300015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font size="2" face="Verdana">17. Perera J., Perera B., Gamage S. Seroconversion    after hepatitis B vaccination in healthy young adults, and the effect of a booster    dose. Ceylon Med J <B>2002</B>;47:6-8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000094&pid=S1413-8670200400020000300016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana"><a name="end"></a><a href="#tx"><img src="/img/revistas/bjid/v8n2/seta.gif" border="0"></a>    <b>Correspondence to</b>    <br>   Dr. Raymundo Paran&aacute;    <br>   Av. Juracy Magalhaes Jr. 2096, Sala 510    <br>   Salvador-Bahia, Brazil, Zip code: 41920-00    <br>   Phone: (5571) 350-4651. Fax: (5571) 353-49800    <br>   E-mail: <a href="mailto:rparana@ufba.br">rparana@ufba.br</a></font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana">Received on 17 August 2003; revised 22 January    2004. </font></p>      ]]></body><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Walsh]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
<name>
<surname><![CDATA[Alexander]]></surname>
<given-names><![CDATA[G.J.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Update on chronic viral hepatitis]]></article-title>
<source><![CDATA[Postgrad Med J]]></source>
<year>2001</year>
<volume>77</volume>
<page-range>498-505</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Holmes-Mc Nary]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Impact factors on development of cirrhosis and subsequent hepatocellular carcinoma]]></article-title>
<source><![CDATA[Compend Contin Educ Dent]]></source>
<year>2001</year>
<volume>22</volume>
<page-range>19-33</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hsu]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
<name>
<surname><![CDATA[Chen]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
<name>
<surname><![CDATA[Chuang]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Efficacy of a mass hepatitis B vaccination program in Taiwan: Studies on 3464 infants of hepatitis B surface antigen-carrier mothers]]></article-title>
<source><![CDATA[JAMA]]></source>
<year>1988</year>
<volume>260</volume>
<page-range>2231-5</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Goh]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
<name>
<surname><![CDATA[Doraisingham]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
<name>
<surname><![CDATA[Tan]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The hepatitis B immunization programme in Singapore]]></article-title>
<source><![CDATA[Bulletin of the World Health Organization]]></source>
<year>1989</year>
<volume>67</volume>
<page-range>65-70</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jilg]]></surname>
<given-names><![CDATA[W.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Preventive vaccination for viral hepatitis]]></article-title>
<source><![CDATA[Zeitschrift für Gastroenterologie]]></source>
<year>1997</year>
<volume>35</volume>
<page-range>585-90</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Souto]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Fontes]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Epidemiological survey of infection with hepatitis B virus in the savanna and wetlands (Pantanal) of central Brazil]]></article-title>
<source><![CDATA[Annals of Tropical Medicine and Parasitology]]></source>
<year>1997</year>
<volume>91</volume>
<page-range>411-6</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Van]]></surname>
<given-names><![CDATA[Herck K.]]></given-names>
</name>
<name>
<surname><![CDATA[Van]]></surname>
<given-names><![CDATA[Damme P.]]></given-names>
</name>
<name>
<surname><![CDATA[Collard]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Thoelen]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Two-dose combined vaccination against hepatitis A and B in healthy subjects aged 11-18 years]]></article-title>
<source><![CDATA[Scandinavian Journal of Gastroenterology]]></source>
<year>1999</year>
<volume>34</volume>
<page-range>1236-40</page-range></nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Emini]]></surname>
<given-names><![CDATA[E.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Ellis]]></surname>
<given-names><![CDATA[R.W.]]></given-names>
</name>
<name>
<surname><![CDATA[Miller]]></surname>
<given-names><![CDATA[W.J.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Production and immunological analysis of recombinant hepatitis B vaccine]]></article-title>
<source><![CDATA[Journal of Infection]]></source>
<year>1986</year>
<volume>13</volume>
<numero>^sA</numero>
<issue>^sA</issue>
<supplement>A</supplement>
<page-range>3-9</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zajac]]></surname>
<given-names><![CDATA[B.A.]]></given-names>
</name>
<name>
<surname><![CDATA[West]]></surname>
<given-names><![CDATA[D.J.]]></given-names>
</name>
<name>
<surname><![CDATA[McAleer]]></surname>
<given-names><![CDATA[W.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Scolnick]]></surname>
<given-names><![CDATA[E.M.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Overview of clinical studies with hepatitis vaccine made by recombinant DNA]]></article-title>
<source><![CDATA[Journal of Infection]]></source>
<year>1986</year>
<volume>13</volume>
<numero>^sA</numero>
<issue>^sA</issue>
<supplement>A</supplement>
<page-range>36-45</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jilg]]></surname>
<given-names><![CDATA[W.]]></given-names>
</name>
<name>
<surname><![CDATA[Schmidt]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[Deinhardt]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Vaccination against hepatitis B: Comparison of three different vaccination schedules]]></article-title>
<source><![CDATA[The Journal of Infectious Diseases]]></source>
<year>1989</year>
<volume>160</volume>
<page-range>766-9</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hadler]]></surname>
<given-names><![CDATA[S.C.]]></given-names>
</name>
<name>
<surname><![CDATA[de Monzon]]></surname>
<given-names><![CDATA[M.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Lugo]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Perez]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effect of timing of hepatitis B vaccine doses on response to vaccine in Yucpa Indians]]></article-title>
<source><![CDATA[Vaccine]]></source>
<year>1989</year>
<volume>7</volume>
<page-range>106-10</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chen]]></surname>
<given-names><![CDATA[C.J.]]></given-names>
</name>
<name>
<surname><![CDATA[You]]></surname>
<given-names><![CDATA[S.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Lin]]></surname>
<given-names><![CDATA[L.H.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cancer epidemiology and control in Taiwan: a brief review]]></article-title>
<source><![CDATA[Jpn J Clin Oncol]]></source>
<year>2002</year>
<volume>32</volume>
<numero>^sS</numero>
<issue>^sS</issue>
<supplement>S</supplement>
<page-range>66-81</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bensabath]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<name>
<surname><![CDATA[Hadler]]></surname>
<given-names><![CDATA[S.C.]]></given-names>
</name>
<name>
<surname><![CDATA[Soares]]></surname>
<given-names><![CDATA[M.C.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Hepatitis delta virus infection and Labrea hepatitis: Prevalence and role in fulminant hepatitis in the Amazon Basin]]></article-title>
<source><![CDATA[JAMA]]></source>
<year>1987</year>
<volume>258</volume>
<page-range>479-83</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Souto]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Fontes]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
<name>
<surname><![CDATA[Gaspar]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Concomitant high prevalence of hepatitis C virus antibody and hepatitis B viral markers in a small village of the Amazon region in Mato Grosso State, Brazil]]></article-title>
<source><![CDATA[Revista do Instituto de Medicina Tropical de São Paulo]]></source>
<year>1996</year>
<volume>38</volume>
<page-range>221-3</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>16</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Liu]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Xu]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[X.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Field epidemiological and experimental study on relationship between genetic factor and nonresponse or hyporesponse to hepatitis B vaccine]]></article-title>
<source><![CDATA[Chin Med J]]></source>
<year>2000</year>
<volume>113</volume>
<page-range>547-50</page-range></nlm-citation>
</ref>
<ref id="B16">
<label>17</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Perera]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Perera]]></surname>
<given-names><![CDATA[B.]]></given-names>
</name>
<name>
<surname><![CDATA[Gamage]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Seroconversion after hepatitis B vaccination in healthy young adults, and the effect of a booster dose]]></article-title>
<source><![CDATA[Ceylon Med J]]></source>
<year>2002</year>
<volume>47</volume>
<page-range>6-8</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
