Efficacy of Double Vaccination With the 2009 Pandemic Influenza A (H1N1) Vaccine During Pregnancy
Identifieur interne : 000975 ( PascalFrancis/Corpus ); précédent : 000974; suivant : 000976Efficacy of Double Vaccination With the 2009 Pandemic Influenza A (H1N1) Vaccine During Pregnancy
Auteurs : Madoka Horiya ; Michi Hisano ; Yoko Iwasaki ; Masachi Hanaoka ; Noriyoshi Watanabe ; Yushi Ito ; Jun Kojima ; Haruhiko Sago ; Atsuko Murashima ; Tatsuo Kato ; Koushi YamaguchiSource :
- Obstetrics and gynecology : (New York. 1953) [ 0029-7844 ] ; 2011.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
OBJECTIVE: To evaluate the efficacy of double vaccination with the 2009 pandemic influenza A (H1N1) vaccine during pregnancy. METHODS: A study of the 2009 H1N1 vaccine was conducted in 128 pregnant women, who were between 8 and 32 weeks of gestation in October 2009, to monitor the immune response to vaccination and the change in antibody positivity rate and to assess the immune response. Furthermore, the study aimed to assess the changes in these parameters after the first and second vaccination, monitor the maintenance of antibody titers in maternal blood, assess antibody transfer to umbilical cord blood, and evaluate the vaccine. RESULTS: The antibody positivity rate increased from 7.2% before vaccination to 89.5% after the second vaccination. The vaccine was efficacious, producing a sufficient immune response in 90% of patients, regardless of the stage of gestation. The antibody titers were maintained until delivery, and were higher in umbilical cord blood at delivery than in maternal blood. Although the second vaccination increased the antibody titers in 27% of patients, and the antibody titers in maternal and umbilical cord blood at delivery tended to be higher in the double vaccination group than in the single, the differences were not statistically significant. CONCLUSION: Single vaccination induces sufficient immune response and transfer of immunity to the fetus in pregnant women with no pre-existing antibodies.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
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Format Inist (serveur)
NO : | PASCAL 11-0444320 INIST |
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ET : | Efficacy of Double Vaccination With the 2009 Pandemic Influenza A (H1N1) Vaccine During Pregnancy |
AU : | HORIYA (Madoka); HISANO (Michi); IWASAKI (Yoko); HANAOKA (Masachi); WATANABE (Noriyoshi); ITO (Yushi); KOJIMA (Jun); SAGO (Haruhiko); MURASHIMA (Atsuko); KATO (Tatsuo); YAMAGUCHI (Koushi) |
AF : | National Center for Child Health and Development and the Japan Drug Information Institute in Pregnancy/Tokyo/Japon (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 8 aut., 9 aut., 10 aut., 11 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Obstetrics and gynecology : (New York. 1953); ISSN 0029-7844; Coden OBGNAS; Etats-Unis; Da. 2011; Vol. 118; No. 4; Pp. 887-894; Bibl. 30 ref. |
LA : | Anglais |
EA : | OBJECTIVE: To evaluate the efficacy of double vaccination with the 2009 pandemic influenza A (H1N1) vaccine during pregnancy. METHODS: A study of the 2009 H1N1 vaccine was conducted in 128 pregnant women, who were between 8 and 32 weeks of gestation in October 2009, to monitor the immune response to vaccination and the change in antibody positivity rate and to assess the immune response. Furthermore, the study aimed to assess the changes in these parameters after the first and second vaccination, monitor the maintenance of antibody titers in maternal blood, assess antibody transfer to umbilical cord blood, and evaluate the vaccine. RESULTS: The antibody positivity rate increased from 7.2% before vaccination to 89.5% after the second vaccination. The vaccine was efficacious, producing a sufficient immune response in 90% of patients, regardless of the stage of gestation. The antibody titers were maintained until delivery, and were higher in umbilical cord blood at delivery than in maternal blood. Although the second vaccination increased the antibody titers in 27% of patients, and the antibody titers in maternal and umbilical cord blood at delivery tended to be higher in the double vaccination group than in the single, the differences were not statistically significant. CONCLUSION: Single vaccination induces sufficient immune response and transfer of immunity to the fetus in pregnant women with no pre-existing antibodies. |
CC : | 002B20; 002B05C02C |
FD : | Immunoprophylaxie; Dédoublement; Vaccination; Prévention; Vaccin; Gestation; Gynécologie; Obstétrique; Grippe H1N1; Virus grippal A(H1N1) |
FG : | Pathologie de l'appareil respiratoire; Virose; Infection |
ED : | Immunoprophylaxis; Double; Vaccination; Prevention; Vaccine; Pregnancy; Gynecology; Obstetrics; H1N1 influenza; Influenza A (H1N1) |
EG : | Respiratory disease; Viral disease; Infection |
SD : | Inmunoprofilaxia; Desdoblamiento; Vacunación; Prevención; Vacuna; Gestación; Ginecología; Obstétrico; Gripe H1N1 |
LO : | INIST-7207.354000509934100170 |
ID : | 11-0444320 |
Links to Exploration step
Pascal:11-0444320Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Efficacy of Double Vaccination With the 2009 Pandemic Influenza A (H1N1) Vaccine During Pregnancy</title>
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<front><div type="abstract" xml:lang="en">OBJECTIVE: To evaluate the efficacy of double vaccination with the 2009 pandemic influenza A (H1N1) vaccine during pregnancy. METHODS: A study of the 2009 H1N1 vaccine was conducted in 128 pregnant women, who were between 8 and 32 weeks of gestation in October 2009, to monitor the immune response to vaccination and the change in antibody positivity rate and to assess the immune response. Furthermore, the study aimed to assess the changes in these parameters after the first and second vaccination, monitor the maintenance of antibody titers in maternal blood, assess antibody transfer to umbilical cord blood, and evaluate the vaccine. RESULTS: The antibody positivity rate increased from 7.2% before vaccination to 89.5% after the second vaccination. The vaccine was efficacious, producing a sufficient immune response in 90% of patients, regardless of the stage of gestation. The antibody titers were maintained until delivery, and were higher in umbilical cord blood at delivery than in maternal blood. Although the second vaccination increased the antibody titers in 27% of patients, and the antibody titers in maternal and umbilical cord blood at delivery tended to be higher in the double vaccination group than in the single, the differences were not statistically significant. CONCLUSION: Single vaccination induces sufficient immune response and transfer of immunity to the fetus in pregnant women with no pre-existing antibodies.</div>
</front>
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<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0029-7844</s0>
</fA01>
<fA02 i1="01"><s0>OBGNAS</s0>
</fA02>
<fA03 i2="1"><s0>Obstet. gynecol. : (N. Y., 1953)</s0>
</fA03>
<fA05><s2>118</s2>
</fA05>
<fA06><s2>4</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Efficacy of Double Vaccination With the 2009 Pandemic Influenza A (H1N1) Vaccine During Pregnancy</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>HORIYA (Madoka)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>HISANO (Michi)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>IWASAKI (Yoko)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>HANAOKA (Masachi)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>WATANABE (Noriyoshi)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>ITO (Yushi)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>KOJIMA (Jun)</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>SAGO (Haruhiko)</s1>
</fA11>
<fA11 i1="09" i2="1"><s1>MURASHIMA (Atsuko)</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>KATO (Tatsuo)</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>YAMAGUCHI (Koushi)</s1>
</fA11>
<fA14 i1="01"><s1>National Center for Child Health and Development and the Japan Drug Information Institute in Pregnancy</s1>
<s2>Tokyo</s2>
<s3>JPN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</fA14>
<fA20><s1>887-894</s1>
</fA20>
<fA21><s1>2011</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>7207</s2>
<s5>354000509934100170</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2011 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>30 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>11-0444320</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Obstetrics and gynecology : (New York. 1953)</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>OBJECTIVE: To evaluate the efficacy of double vaccination with the 2009 pandemic influenza A (H1N1) vaccine during pregnancy. METHODS: A study of the 2009 H1N1 vaccine was conducted in 128 pregnant women, who were between 8 and 32 weeks of gestation in October 2009, to monitor the immune response to vaccination and the change in antibody positivity rate and to assess the immune response. Furthermore, the study aimed to assess the changes in these parameters after the first and second vaccination, monitor the maintenance of antibody titers in maternal blood, assess antibody transfer to umbilical cord blood, and evaluate the vaccine. RESULTS: The antibody positivity rate increased from 7.2% before vaccination to 89.5% after the second vaccination. The vaccine was efficacious, producing a sufficient immune response in 90% of patients, regardless of the stage of gestation. The antibody titers were maintained until delivery, and were higher in umbilical cord blood at delivery than in maternal blood. Although the second vaccination increased the antibody titers in 27% of patients, and the antibody titers in maternal and umbilical cord blood at delivery tended to be higher in the double vaccination group than in the single, the differences were not statistically significant. CONCLUSION: Single vaccination induces sufficient immune response and transfer of immunity to the fetus in pregnant women with no pre-existing antibodies.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B20</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B05C02C</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Immunoprophylaxie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Immunoprophylaxis</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Inmunoprofilaxia</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Dédoublement</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Double</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Desdoblamiento</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Vaccination</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Vaccination</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Vacunación</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Prévention</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Prevention</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Prevención</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Vaccin</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Vaccine</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Vacuna</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Gestation</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Pregnancy</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Gestación</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Gynécologie</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Gynecology</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Ginecología</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Obstétrique</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Obstetrics</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Obstétrico</s0>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Grippe H1N1</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>H1N1 influenza</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Gripe H1N1</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Virus grippal A(H1N1)</s0>
<s4>CD</s4>
<s5>97</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Influenza A (H1N1)</s0>
<s4>CD</s4>
<s5>97</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Respiratory disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Virose</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Viral disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Virosis</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Infection</s0>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Infection</s0>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Infección</s0>
</fC07>
<fN21><s1>305</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
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<server><NO>PASCAL 11-0444320 INIST</NO>
<ET>Efficacy of Double Vaccination With the 2009 Pandemic Influenza A (H1N1) Vaccine During Pregnancy</ET>
<AU>HORIYA (Madoka); HISANO (Michi); IWASAKI (Yoko); HANAOKA (Masachi); WATANABE (Noriyoshi); ITO (Yushi); KOJIMA (Jun); SAGO (Haruhiko); MURASHIMA (Atsuko); KATO (Tatsuo); YAMAGUCHI (Koushi)</AU>
<AF>National Center for Child Health and Development and the Japan Drug Information Institute in Pregnancy/Tokyo/Japon (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 8 aut., 9 aut., 10 aut., 11 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Obstetrics and gynecology : (New York. 1953); ISSN 0029-7844; Coden OBGNAS; Etats-Unis; Da. 2011; Vol. 118; No. 4; Pp. 887-894; Bibl. 30 ref.</SO>
<LA>Anglais</LA>
<EA>OBJECTIVE: To evaluate the efficacy of double vaccination with the 2009 pandemic influenza A (H1N1) vaccine during pregnancy. METHODS: A study of the 2009 H1N1 vaccine was conducted in 128 pregnant women, who were between 8 and 32 weeks of gestation in October 2009, to monitor the immune response to vaccination and the change in antibody positivity rate and to assess the immune response. Furthermore, the study aimed to assess the changes in these parameters after the first and second vaccination, monitor the maintenance of antibody titers in maternal blood, assess antibody transfer to umbilical cord blood, and evaluate the vaccine. RESULTS: The antibody positivity rate increased from 7.2% before vaccination to 89.5% after the second vaccination. The vaccine was efficacious, producing a sufficient immune response in 90% of patients, regardless of the stage of gestation. The antibody titers were maintained until delivery, and were higher in umbilical cord blood at delivery than in maternal blood. Although the second vaccination increased the antibody titers in 27% of patients, and the antibody titers in maternal and umbilical cord blood at delivery tended to be higher in the double vaccination group than in the single, the differences were not statistically significant. CONCLUSION: Single vaccination induces sufficient immune response and transfer of immunity to the fetus in pregnant women with no pre-existing antibodies.</EA>
<CC>002B20; 002B05C02C</CC>
<FD>Immunoprophylaxie; Dédoublement; Vaccination; Prévention; Vaccin; Gestation; Gynécologie; Obstétrique; Grippe H1N1; Virus grippal A(H1N1)</FD>
<FG>Pathologie de l'appareil respiratoire; Virose; Infection</FG>
<ED>Immunoprophylaxis; Double; Vaccination; Prevention; Vaccine; Pregnancy; Gynecology; Obstetrics; H1N1 influenza; Influenza A (H1N1)</ED>
<EG>Respiratory disease; Viral disease; Infection</EG>
<SD>Inmunoprofilaxia; Desdoblamiento; Vacunación; Prevención; Vacuna; Gestación; Ginecología; Obstétrico; Gripe H1N1</SD>
<LO>INIST-7207.354000509934100170</LO>
<ID>11-0444320</ID>
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