Randomized controlled trial of seroresponses to double dose and booster influenza vaccination in frail elderly subjects
Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccinat...
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Published in | Journal of medical virology Vol. 63; no. 4; pp. 293 - 298 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
John Wiley & Sons, Inc
01.04.2001
Wiley-Liss |
Subjects | |
Online Access | Get full text |
ISSN | 0146-6615 1096-9071 |
DOI | 10.1002/1096-9071(200104)63:4<293::AID-JMV1004>3.0.CO;2-C |
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Abstract | Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccination. A total of 815 patients (median age 83 years, median disability score 8, median disease categories 2 and median number of medications 4) residing in 14 nursing homes in the Netherlands were vaccinated during the influenza season 1997–98. The first vaccine dose (15 or 30 μg) was given on Day 0 followed by a booster dose (placebo or 15 μg) on Day 84. Blood samples were taken before and 25 days after vaccination. There were four treatment groups: (i) 15 μg and placebo, (ii) 15 μg and 15 μg booster, (iii) 30 μg and placebo and (iv) 30 μg and 15 μg booster. Geometric mean antibody titers of those receiving the double vaccine dose was 15% (95% CI, 6% to 24%, P = 0.001) higher as compared to the standard 15 μg dose. A booster dose, given 84 days after the first vaccination, yielded postvaccination titters that were 14% (95% CI, 9% to 19%, P = 0.001) higher as compared to placebo. Subgroup analysis did not reveal patient groups that had a proportionally greater benefit from adapted vaccination strategies. It is concluded that higher antibody responses can be achieved in frail elderly people by a double vaccine dose or a booster vaccination. J. Med. Virol. 63:293–298, 2001. © 2001 Wiley‐Liss, Inc. |
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AbstractList | Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccination. A total of 815 patients (median age 83 years, median disability score 8, median disease categories 2 and median number of medications 4) residing in 14 nursing homes in the Netherlands were vaccinated during the influenza season 1997-98. The first vaccine dose (15 or 30 microg) was given on Day 0 followed by a booster dose (placebo or 15 microg) on Day 84. Blood samples were taken before and 25 days after vaccination. There were four treatment groups: (i) 15 microg and placebo, (ii) 15 microg and 15 microg booster, (iii) 30 microg and placebo and (iv) 30 microg and 15 microg booster. Geometric mean antibody titers of those receiving the double vaccine dose was 15% (95% CI, 6% to 24%, P = 0.001) higher as compared to the standard 15 microg dose. A booster dose, given 84 days after the first vaccination, yielded postvaccination titters that were 14% (95% CI, 9% to 19%, P = 0.001) higher as compared to placebo. Subgroup analysis did not reveal patient groups that had a proportionally greater benefit from adapted vaccination strategies. It is concluded that higher antibody responses can be achieved in frail elderly people by a double vaccine dose or a booster vaccination. Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccination. A total of 815 patients (median age 83 years, median disability score 8, median disease categories 2 and median number of medications 4) residing in 14 nursing homes in the Netherlands were vaccinated during the influenza season 1997–98. The first vaccine dose (15 or 30 μg) was given on Day 0 followed by a booster dose (placebo or 15 μg) on Day 84. Blood samples were taken before and 25 days after vaccination. There were four treatment groups: (i) 15 μg and placebo, (ii) 15 μg and 15 μg booster, (iii) 30 μg and placebo and (iv) 30 μg and 15 μg booster. Geometric mean antibody titers of those receiving the double vaccine dose was 15% (95% CI, 6% to 24%, P = 0.001) higher as compared to the standard 15 μg dose. A booster dose, given 84 days after the first vaccination, yielded postvaccination titters that were 14% (95% CI, 9% to 19%, P = 0.001) higher as compared to placebo. Subgroup analysis did not reveal patient groups that had a proportionally greater benefit from adapted vaccination strategies. It is concluded that higher antibody responses can be achieved in frail elderly people by a double vaccine dose or a booster vaccination. J. Med. Virol. 63:293–298, 2001. © 2001 Wiley‐Liss, Inc. Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccination. A total of 815 patients (median age 83 years, median disability score 8, median disease categories 2 and median number of medications 4) residing in 14 nursing homes in the Netherlands were vaccinated during the influenza season 1997-98. The first vaccine dose (15 or 30 mu g) was given on Day 0 followed by a booster dose (placebo or 15 mu g) on Day 84. Blood samples were taken before and 25 days after vaccination. There were four treatment groups: (i) 15 mu g and placebo, (ii) 15 mu g and 15 mu g booster, (iii) 30 mu g and placebo and (iv) 30 mu g and 15 mu g booster. Geometric mean antibody titers of those receiving the double vaccine dose was 15% (95% Cl, 6% to 24%, P=0.001) higher as compared to the standard 15 mu g dose. A booster dose, given 84 days after the first vaccination, yielded postvaccination titters that were 14% (95% Cl, 9% to 19%, P=0.001) higher as compared to placebo. Subgroup analysis did not reveal patient groups that had a proportionally greater benefit from adapted vaccination strategies. It is concluded that higher antibody responses can be achieved in frail elderly people by a double vaccine dose or a booster vaccination. Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccination. A total of 815 patients (median age 83 years, median disability score 8, median disease categories 2 and median number of medications 4) residing in 14 nursing homes in the Netherlands were vaccinated during the influenza season 1997-98. The first vaccine dose (15 or 30 microg) was given on Day 0 followed by a booster dose (placebo or 15 microg) on Day 84. Blood samples were taken before and 25 days after vaccination. There were four treatment groups: (i) 15 microg and placebo, (ii) 15 microg and 15 microg booster, (iii) 30 microg and placebo and (iv) 30 microg and 15 microg booster. Geometric mean antibody titers of those receiving the double vaccine dose was 15% (95% CI, 6% to 24%, P = 0.001) higher as compared to the standard 15 microg dose. A booster dose, given 84 days after the first vaccination, yielded postvaccination titters that were 14% (95% CI, 9% to 19%, P = 0.001) higher as compared to placebo. Subgroup analysis did not reveal patient groups that had a proportionally greater benefit from adapted vaccination strategies. It is concluded that higher antibody responses can be achieved in frail elderly people by a double vaccine dose or a booster vaccination.Responses to influenza vaccination are poor in frail elderly subjects who suffer the greatest morbidity and mortality due to infection. Therefore, a randomized clinical trial was performed to determine the effect of a double dose and booster vaccination on antibody responses after influenza vaccination. A total of 815 patients (median age 83 years, median disability score 8, median disease categories 2 and median number of medications 4) residing in 14 nursing homes in the Netherlands were vaccinated during the influenza season 1997-98. The first vaccine dose (15 or 30 microg) was given on Day 0 followed by a booster dose (placebo or 15 microg) on Day 84. Blood samples were taken before and 25 days after vaccination. There were four treatment groups: (i) 15 microg and placebo, (ii) 15 microg and 15 microg booster, (iii) 30 microg and placebo and (iv) 30 microg and 15 microg booster. Geometric mean antibody titers of those receiving the double vaccine dose was 15% (95% CI, 6% to 24%, P = 0.001) higher as compared to the standard 15 microg dose. A booster dose, given 84 days after the first vaccination, yielded postvaccination titters that were 14% (95% CI, 9% to 19%, P = 0.001) higher as compared to placebo. Subgroup analysis did not reveal patient groups that had a proportionally greater benefit from adapted vaccination strategies. It is concluded that higher antibody responses can be achieved in frail elderly people by a double vaccine dose or a booster vaccination. |
Author | Remarque, E.J. Knook, D.L. Westendorp, R.G.J. Cools, H.J.M. Roos-van Eijndhoven, D.G. Ten Cate-Hoek, A.J. |
Author_xml | – sequence: 1 givenname: D.G. surname: Roos-van Eijndhoven fullname: Roos-van Eijndhoven, D.G. organization: Department of General Practice and Nursing Home Medicine, Leiden University Medical Center, The Netherlands – sequence: 2 givenname: H.J.M. surname: Cools fullname: Cools, H.J.M. organization: Department of General Practice and Nursing Home Medicine, Leiden University Medical Center, The Netherlands – sequence: 3 givenname: R.G.J. surname: Westendorp fullname: Westendorp, R.G.J. organization: Section of Gerontology, Dept. of Internal Medicine, Leiden University Medical Center, The Netherlands – sequence: 4 givenname: A.J. surname: Ten Cate-Hoek fullname: Ten Cate-Hoek, A.J. organization: Psychogeriatric Nursing Home Mariahoeve, The Hague, The Netherlands – sequence: 5 givenname: D.L. surname: Knook fullname: Knook, D.L. organization: Section of Gerontology, Dept. of Internal Medicine, Leiden University Medical Center, The Netherlands – sequence: 6 givenname: E.J. surname: Remarque fullname: Remarque, E.J. email: E.J.Remarque@LUMC.NL organization: Section of Gerontology, Dept. of Internal Medicine, Leiden University Medical Center, The Netherlands |
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Keywords | Human Immunoprotection Booster vaccination Vaccination Orthomyxoviridae Vaccine Influenzavirus Dose activity relation Virus Immunogenicity Clinical trial Elderly Humoral immunity |
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Notes | Informed consent was obtained from all participants of the current study. Guidelines for human experimentation of the Leiden University were followed in the conduct of the research. The study was approved by the Leiden University Medical Ethics Committee. ark:/67375/WNG-2L9L2QMX-6 ArticleID:JMV1004 istex:7F821C57D29E6D321A4C02626E1EB70C024E0C6A Praeventiefonds - No. 28-2732 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 |
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JAMA 253:1136-1139. 1994; 331 1990; 13 1991; 133 1986; 153 1989; 7 1988; 36 1994; 272 1970; 10 1998; 158 1972; 46 1988; 128 1993; 167 1990; 161 1987; 25 1989; 103 1987; 137 1993; 11 1999; 34 1972; 70 1999; 179 1992; 21 1996; 312 1980; 244 1998; 55 1992; 40 1985; 253 Powers (BIB21) 1992; 40 Govaert (BIB7) 1994; 272 Reuman (BIB26) 1990; 13 Longini (BIB13) 1988; 128 Sullivan (BIB28) 1990; 161 Glezen (BIB6) 1991; 133 Beyer (BIB3) 1989; 7 Gross (BIB8) 1988; 36 Powers (BIB20) 1993; 167 Remarque (BIB25) 1999; 34 Hobson (BIB10) 1972; 70 Coles (BIB5) 1992; 40 Arden (BIB1) 1986; 153 Remarque (BIB24) 1998; 55 Nichol (BIB14) 1994; 331 Levine (BIB12) 1987; 137 Barker (BIB2) 1980; 244 Nicholson (BIB16) 1992; 21 Wesselius-de Casparis (BIB29) 1972; 46 Remarque (BIB22) 1993; 11 Gross (BIB9) 1987; 25 Peters (BIB19) 1988; 36 de Bruijn (BIB4) 1999; 179 Nichol (BIB15) 1998; 158 Remarque (BIB23) 1996; 312 Katz (BIB11) 1970; 10 Palache (BIB17) 1993; 11 Patriarca (BIB18) 1985; 253 Sprenger (BIB27) 1989; 103 |
References_xml | – reference: Beyer WEPh, Palache AM, Baljet M, Masurel N. 1989. Antibody induction by influenza vaccines in the elderly: a review of the literature. Vaccine 7:385-394. – reference: Remarque EJ, de Bruijn IA, Boersma WJA, Masurel N, Ligthart GJ. 1998. Altered antibody response to influenza H1N1 vaccine in healthy elderly people as determined by HI, ELISA, and neutralization assay. J Med Virol 55:82-87. – reference: Hobson D, Curry RL, Beare AS, Ward-Gardner A. 1972. The role of serum hemagglutination-inhibiting antibody in protection against challenge infection with influenza A2 and B viruses. Journal of Hygiene Cambridge 70:767-777. – reference: Remarque EJ, de Jong JM, van der Klis RJ, Masurel N, Ligthart GJ. 1999. Dose-dependent antibody response to influenza H1N1 vaccine component in elderly nursing home patients. Exp Gerontol 34:109-115. – reference: Peters NL, Meiklejohn G, Jahnigen DW. 1988. 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SubjectTerms | Aged Aged, 80 and over Antibodies, Viral - blood Biological and medical sciences Epidemiology. Vaccinations Female General aspects Humans immunization Immunization, Secondary Infectious diseases influenza Influenza A virus - immunology Influenza B virus - immunology Influenza Vaccines - administration & dosage Influenza virus Influenza, Human - blood Influenza, Human - epidemiology Influenza, Human - prevention & control Male Medical sciences Netherlands - epidemiology nursing home Orthomyxoviridae - immunology randomized controlled trial Vaccination |
Title | Randomized controlled trial of seroresponses to double dose and booster influenza vaccination in frail elderly subjects |
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