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Safety and Immune Responses in Children After Concurrent or Sequential 2009 H1N1 and 2009-2010 Seasonal Trivalent Influenza Vaccinations

Identifieur interne : 000524 ( PascalFrancis/Corpus ); précédent : 000523; suivant : 000525

Safety and Immune Responses in Children After Concurrent or Sequential 2009 H1N1 and 2009-2010 Seasonal Trivalent Influenza Vaccinations

Auteurs : Sharon E. Frey ; David I. Bernstein ; Michael A. Gerber ; Harry L. Keyserling ; Flor M. Munoz ; Patricia L. Winokur ; Christine B. Turley ; Richard E. Rupp ; Heather Hill ; Mark Wolff ; Diana L. Noah ; Allison C. Ross ; Gretchen Cress ; Robert B. Belshe

Source :

RBID : Pascal:12-0371849

Descripteurs français

English descriptors

Abstract

Background. Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children. Methods. Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored. Results. All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine. Conclusions. Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0022-1899
A02 01      @0 JIDIAQ
A03   1    @0 J. infect. dis.
A05       @2 206
A06       @2 6
A08 01  1  ENG  @1 Safety and Immune Responses in Children After Concurrent or Sequential 2009 H1N1 and 2009-2010 Seasonal Trivalent Influenza Vaccinations
A11 01  1    @1 FREY (Sharon E.)
A11 02  1    @1 BERNSTEIN (David I.)
A11 03  1    @1 GERBER (Michael A.)
A11 04  1    @1 KEYSERLING (Harry L.)
A11 05  1    @1 MUNOZ (Flor M.)
A11 06  1    @1 WINOKUR (Patricia L.)
A11 07  1    @1 TURLEY (Christine B.)
A11 08  1    @1 RUPP (Richard E.)
A11 09  1    @1 HILL (Heather)
A11 10  1    @1 WOLFF (Mark)
A11 11  1    @1 NOAH (Diana L.)
A11 12  1    @1 ROSS (Allison C.)
A11 13  1    @1 CRESS (Gretchen)
A11 14  1    @1 BELSHE (Robert B.)
A14 01      @1 Saint Louis University School of Medicine @2 Missouri @3 USA @Z 1 aut. @Z 14 aut.
A14 02      @1 Cincinnati Children's Hospital Medical Center @2 Ohio @3 USA @Z 2 aut. @Z 3 aut.
A14 03      @1 Emory University School of Medicine and Children's Healthcare of Atlanta @3 GEO @Z 4 aut. @Z 12 aut.
A14 04      @1 Baylor College of Medicine @2 Houston, Texas @3 USA @Z 5 aut.
A14 05      @1 University of Iowa, Carver College of Medicine @2 Iowa City @3 USA @Z 6 aut. @Z 13 aut.
A14 06      @1 University of Texas Medical Branch-Galveston @3 USA @Z 7 aut. @Z 8 aut.
A14 07      @1 The EMMES Corporation @2 Rockville, Maryland @3 USA @Z 9 aut. @Z 10 aut.
A14 08      @1 Southern Research Institute @2 Birmingham, Alabama @3 USA @Z 11 aut.
A20       @1 828-837
A21       @1 2012
A23 01      @0 ENG
A43 01      @1 INIST @2 2052 @5 354000509502200060
A44       @0 0000 @1 © 2012 INIST-CNRS. All rights reserved.
A45       @0 24 ref.
A47 01  1    @0 12-0371849
A60       @1 P
A61       @0 A
A64 01  1    @0 The Journal of infectious diseases
A66 01      @0 GBR
C01 01    ENG  @0 Background. Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children. Methods. Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored. Results. All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine. Conclusions. Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.
C02 01  X    @0 002A05
C02 02  X    @0 002B05
C03 01  X  FRE  @0 Réponse immune @5 05
C03 01  X  ENG  @0 Immune response @5 05
C03 01  X  SPA  @0 Respuesta inmune @5 05
C03 02  X  FRE  @0 Enfant @5 06
C03 02  X  ENG  @0 Child @5 06
C03 02  X  SPA  @0 Niño @5 06
C03 03  X  FRE  @0 Vaccination @5 07
C03 03  X  ENG  @0 Vaccination @5 07
C03 03  X  SPA  @0 Vacunación @5 07
C03 04  X  FRE  @0 Infection @5 08
C03 04  X  ENG  @0 Infection @5 08
C03 04  X  SPA  @0 Infección @5 08
C03 05  X  FRE  @0 Grippe @5 14
C03 05  X  ENG  @0 Influenza @5 14
C03 05  X  SPA  @0 Gripe @5 14
C03 06  X  FRE  @0 Virus grippal A(H1N1) @4 CD @5 96
C03 06  X  ENG  @0 Influenzavirus A(H1N1) @4 CD @5 96
C07 01  X  FRE  @0 Homme
C07 01  X  ENG  @0 Human
C07 01  X  SPA  @0 Hombre
C07 02  X  FRE  @0 Virose
C07 02  X  ENG  @0 Viral disease
C07 02  X  SPA  @0 Virosis
N21       @1 289
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 12-0371849 INIST
ET : Safety and Immune Responses in Children After Concurrent or Sequential 2009 H1N1 and 2009-2010 Seasonal Trivalent Influenza Vaccinations
AU : FREY (Sharon E.); BERNSTEIN (David I.); GERBER (Michael A.); KEYSERLING (Harry L.); MUNOZ (Flor M.); WINOKUR (Patricia L.); TURLEY (Christine B.); RUPP (Richard E.); HILL (Heather); WOLFF (Mark); NOAH (Diana L.); ROSS (Allison C.); CRESS (Gretchen); BELSHE (Robert B.)
AF : Saint Louis University School of Medicine/Missouri/Etats-Unis (1 aut., 14 aut.); Cincinnati Children's Hospital Medical Center/Ohio/Etats-Unis (2 aut., 3 aut.); Emory University School of Medicine and Children's Healthcare of Atlanta/Géorgie (4 aut., 12 aut.); Baylor College of Medicine/Houston, Texas/Etats-Unis (5 aut.); University of Iowa, Carver College of Medicine/Iowa City/Etats-Unis (6 aut., 13 aut.); University of Texas Medical Branch-Galveston/Etats-Unis (7 aut., 8 aut.); The EMMES Corporation/Rockville, Maryland/Etats-Unis (9 aut., 10 aut.); Southern Research Institute/Birmingham, Alabama/Etats-Unis (11 aut.)
DT : Publication en série; Niveau analytique
SO : The Journal of infectious diseases; ISSN 0022-1899; Coden JIDIAQ; Royaume-Uni; Da. 2012; Vol. 206; No. 6; Pp. 828-837; Bibl. 24 ref.
LA : Anglais
EA : Background. Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children. Methods. Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored. Results. All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine. Conclusions. Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.
CC : 002A05; 002B05
FD : Réponse immune; Enfant; Vaccination; Infection; Grippe; Virus grippal A(H1N1)
FG : Homme; Virose
ED : Immune response; Child; Vaccination; Infection; Influenza; Influenzavirus A(H1N1)
EG : Human; Viral disease
SD : Respuesta inmune; Niño; Vacunación; Infección; Gripe
LO : INIST-2052.354000509502200060
ID : 12-0371849

Links to Exploration step

Pascal:12-0371849

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<div type="abstract" xml:lang="en">Background. Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children. Methods. Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored. Results. All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine. Conclusions. Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.</div>
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<s1>GERBER (Michael A.)</s1>
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<fA11 i1="09" i2="1">
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<fA11 i1="11" i2="1">
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<s1>ROSS (Allison C.)</s1>
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<fA11 i1="13" i2="1">
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<s2>Missouri</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>14 aut.</sZ>
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<s1>Cincinnati Children's Hospital Medical Center</s1>
<s2>Ohio</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
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<fA14 i1="03">
<s1>Emory University School of Medicine and Children's Healthcare of Atlanta</s1>
<s3>GEO</s3>
<sZ>4 aut.</sZ>
<sZ>12 aut.</sZ>
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<fA14 i1="04">
<s1>Baylor College of Medicine</s1>
<s2>Houston, Texas</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>University of Iowa, Carver College of Medicine</s1>
<s2>Iowa City</s2>
<s3>USA</s3>
<sZ>6 aut.</sZ>
<sZ>13 aut.</sZ>
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<fA14 i1="06">
<s1>University of Texas Medical Branch-Galveston</s1>
<s3>USA</s3>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
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<s3>USA</s3>
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<sZ>10 aut.</sZ>
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<s0>12-0371849</s0>
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<fA66 i1="01">
<s0>GBR</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Background. Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children. Methods. Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored. Results. All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine. Conclusions. Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.</s0>
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<fC02 i1="02" i2="X">
<s0>002B05</s0>
</fC02>
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<s0>Réponse immune</s0>
<s5>05</s5>
</fC03>
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<s0>Immune response</s0>
<s5>05</s5>
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<s5>05</s5>
</fC03>
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<s5>06</s5>
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<s5>07</s5>
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<s5>07</s5>
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<s0>Infection</s0>
<s5>08</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Infection</s0>
<s5>08</s5>
</fC03>
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<s0>Infección</s0>
<s5>08</s5>
</fC03>
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<s0>Grippe</s0>
<s5>14</s5>
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<s0>Influenza</s0>
<s5>14</s5>
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<s0>Gripe</s0>
<s5>14</s5>
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<s0>Virus grippal A(H1N1)</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Influenzavirus A(H1N1)</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Homme</s0>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Human</s0>
</fC07>
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<s0>Hombre</s0>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Virose</s0>
</fC07>
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<s0>Viral disease</s0>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Virosis</s0>
</fC07>
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<ET>Safety and Immune Responses in Children After Concurrent or Sequential 2009 H1N1 and 2009-2010 Seasonal Trivalent Influenza Vaccinations</ET>
<AU>FREY (Sharon E.); BERNSTEIN (David I.); GERBER (Michael A.); KEYSERLING (Harry L.); MUNOZ (Flor M.); WINOKUR (Patricia L.); TURLEY (Christine B.); RUPP (Richard E.); HILL (Heather); WOLFF (Mark); NOAH (Diana L.); ROSS (Allison C.); CRESS (Gretchen); BELSHE (Robert B.)</AU>
<AF>Saint Louis University School of Medicine/Missouri/Etats-Unis (1 aut., 14 aut.); Cincinnati Children's Hospital Medical Center/Ohio/Etats-Unis (2 aut., 3 aut.); Emory University School of Medicine and Children's Healthcare of Atlanta/Géorgie (4 aut., 12 aut.); Baylor College of Medicine/Houston, Texas/Etats-Unis (5 aut.); University of Iowa, Carver College of Medicine/Iowa City/Etats-Unis (6 aut., 13 aut.); University of Texas Medical Branch-Galveston/Etats-Unis (7 aut., 8 aut.); The EMMES Corporation/Rockville, Maryland/Etats-Unis (9 aut., 10 aut.); Southern Research Institute/Birmingham, Alabama/Etats-Unis (11 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>The Journal of infectious diseases; ISSN 0022-1899; Coden JIDIAQ; Royaume-Uni; Da. 2012; Vol. 206; No. 6; Pp. 828-837; Bibl. 24 ref.</SO>
<LA>Anglais</LA>
<EA>Background. Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children. Methods. Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored. Results. All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine. Conclusions. Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.</EA>
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<FG>Homme; Virose</FG>
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