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    <title>Monninkhof, E.</title>
    <link>http://repub.eur.nl/res/aut/1221/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
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    <item>
      <title>Host-pathogen interaction during pneumococcal infection in patients with chronic obstructive pulmonary disease (Article)</title>
      <link>http://repub.eur.nl/res/pub/10303/</link>
      <pubDate>2004-01-01T00:00:00Z</pubDate>
      <description>Acute exacerbation is a frequent complication of chronic obstructive
      pulmonary disease (COPD). Recent studies suggested a role for bacteria
      such as Streptococcus pneumoniae in the development of acute exacerbation.
      For this study, we investigated the following in COPD patients: (i) the
      epidemiology of pneumococcal colonization and infection, (ii) the effect
      of pneumococcal colonization on the development of exacerbation, and (iii)
      the immunological response against S. pneumoniae. We cultured sputa of 269
      COPD patients during a stable state and during exacerbation of COPD and
      characterized 115 pneumococcal isolates by use of serotyping. Moreover, we
      studied serum immunoglobulin G (IgG) antibody titers, antibody avidities,
      and functional antibody titers against the seven conjugate vaccine
      serotypes in these patients. Colonization with only pneumococci
      (monocultures) increased the risk of exacerbation, with a hazard ratio of
      2.93 (95% confidence interval, 1.41 to 6.07). The most prevalent
      pneumococcal serotypes found were serotypes 19F, 3, 14, 9L/N/V, 23A/B, and
      11. We calculated the theoretical coverage for the 7- and 11-valent
      pneumococcal vaccines to be 60 and 73%, respectively. All patients had
      detectable IgG levels against the seven conjugate vaccine serotypes. These
      antibody titers were significantly lower than those in vaccinated healthy
      adults. Finally, on average, a 2.5-fold rise in serotype-specific and
      functional antibodies in S. pneumoniae-positive sputum cultures was
      observed during exacerbation. Our data indicate that pneumococcal
      colonization in COPD patients is frequently caused by vaccine serotype
      strains. Moreover, pneumococcal colonization is a risk factor for
      exacerbation of COPD. Finally, our findings demonstrate that COPD patients
      are able to mount a significant immune response to pneumococcal infection.
      COPD patients may therefore benefit from pneumococcal vaccination.</description>
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