Vaccinology: time to change the paradigm?

Research output: Contribution to journalReviewResearchpeer-review

Standard

Vaccinology : time to change the paradigm? / Benn, Christine Stabell; Fisker, Ane B; Rieckmann, Andreas; Sørup, Signe; Aaby, Peter.

In: Lancet Infectious Diseases, Vol. 20, No. 10, 2020, p. e274-e283.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Benn, CS, Fisker, AB, Rieckmann, A, Sørup, S & Aaby, P 2020, 'Vaccinology: time to change the paradigm?', Lancet Infectious Diseases, vol. 20, no. 10, pp. e274-e283. https://doi.org/10.1016/S1473-3099(19)30742-X

APA

Benn, C. S., Fisker, A. B., Rieckmann, A., Sørup, S., & Aaby, P. (2020). Vaccinology: time to change the paradigm? Lancet Infectious Diseases, 20(10), e274-e283. https://doi.org/10.1016/S1473-3099(19)30742-X

Vancouver

Benn CS, Fisker AB, Rieckmann A, Sørup S, Aaby P. Vaccinology: time to change the paradigm? Lancet Infectious Diseases. 2020;20(10):e274-e283. https://doi.org/10.1016/S1473-3099(19)30742-X

Author

Benn, Christine Stabell ; Fisker, Ane B ; Rieckmann, Andreas ; Sørup, Signe ; Aaby, Peter. / Vaccinology : time to change the paradigm?. In: Lancet Infectious Diseases. 2020 ; Vol. 20, No. 10. pp. e274-e283.

Bibtex

@article{619b8262e7d44a3b9e1d7d6eefe1480e,
title = "Vaccinology: time to change the paradigm?",
abstract = "The existing vaccine paradigm assumes that vaccines only protect against the target infection, that effective vaccines reduce mortality corresponding to the target infection's share of total mortality, and that the effects of vaccines are similar for males and females. However, epidemiological vaccine research has generated observations that contradict these assumptions and suggest that vaccines have important non-specific effects on overall health in populations. These include the observations that several live vaccines reduce the incidence of all-cause mortality in vaccinated compared with unvaccinated populations far more than can be explained by protection against the target infections, and that several non-live vaccines are associated with increased all-cause mortality in females. In this Personal View we describe current observations and contradictions and define six emerging principles that might explain them. First, that live vaccines enhance resistance towards unrelated infections. Second, non-live vaccines enhance the susceptibility of girls to unrelated infections. Third, the most recently administered vaccination has the strongest non-specific effects. Fourth, combinations of live and non-live vaccines given together have variable non-specific health effects. Fifth, vaccinating children with live vaccines in the presence of maternal immunity enhances beneficial non-specific effects and reduces mortality. Finally, vaccines might interact with other co-administered health interventions, for example vitamin A supplementation. The potential implications for child health are substantial. For example, if BCG vaccination was given to children at birth, if higher measles vaccination coverage could be obtained, if diphtheria, tetanus, and pertussis-containing vaccines were not given with or after measles vaccine, or if the BCG strain with the best non-specific effects could be used consistently, then child mortality could be considerably lower. Pursuing these emerging principles could improve our understanding and use of vaccines globally.",
keywords = "Child, Child Mortality, Humans, Vaccination, Vaccines/administration & dosage",
author = "Benn, {Christine Stabell} and Fisker, {Ane B} and Andreas Rieckmann and Signe S{\o}rup and Peter Aaby",
note = "Copyright {\textcopyright} 2020 Elsevier Ltd. All rights reserved.",
year = "2020",
doi = "10.1016/S1473-3099(19)30742-X",
language = "English",
volume = "20",
pages = "e274--e283",
journal = "The Lancet Infectious Diseases",
issn = "1473-3099",
publisher = "TheLancet Publishing Group",
number = "10",

}

RIS

TY - JOUR

T1 - Vaccinology

T2 - time to change the paradigm?

AU - Benn, Christine Stabell

AU - Fisker, Ane B

AU - Rieckmann, Andreas

AU - Sørup, Signe

AU - Aaby, Peter

N1 - Copyright © 2020 Elsevier Ltd. All rights reserved.

PY - 2020

Y1 - 2020

N2 - The existing vaccine paradigm assumes that vaccines only protect against the target infection, that effective vaccines reduce mortality corresponding to the target infection's share of total mortality, and that the effects of vaccines are similar for males and females. However, epidemiological vaccine research has generated observations that contradict these assumptions and suggest that vaccines have important non-specific effects on overall health in populations. These include the observations that several live vaccines reduce the incidence of all-cause mortality in vaccinated compared with unvaccinated populations far more than can be explained by protection against the target infections, and that several non-live vaccines are associated with increased all-cause mortality in females. In this Personal View we describe current observations and contradictions and define six emerging principles that might explain them. First, that live vaccines enhance resistance towards unrelated infections. Second, non-live vaccines enhance the susceptibility of girls to unrelated infections. Third, the most recently administered vaccination has the strongest non-specific effects. Fourth, combinations of live and non-live vaccines given together have variable non-specific health effects. Fifth, vaccinating children with live vaccines in the presence of maternal immunity enhances beneficial non-specific effects and reduces mortality. Finally, vaccines might interact with other co-administered health interventions, for example vitamin A supplementation. The potential implications for child health are substantial. For example, if BCG vaccination was given to children at birth, if higher measles vaccination coverage could be obtained, if diphtheria, tetanus, and pertussis-containing vaccines were not given with or after measles vaccine, or if the BCG strain with the best non-specific effects could be used consistently, then child mortality could be considerably lower. Pursuing these emerging principles could improve our understanding and use of vaccines globally.

AB - The existing vaccine paradigm assumes that vaccines only protect against the target infection, that effective vaccines reduce mortality corresponding to the target infection's share of total mortality, and that the effects of vaccines are similar for males and females. However, epidemiological vaccine research has generated observations that contradict these assumptions and suggest that vaccines have important non-specific effects on overall health in populations. These include the observations that several live vaccines reduce the incidence of all-cause mortality in vaccinated compared with unvaccinated populations far more than can be explained by protection against the target infections, and that several non-live vaccines are associated with increased all-cause mortality in females. In this Personal View we describe current observations and contradictions and define six emerging principles that might explain them. First, that live vaccines enhance resistance towards unrelated infections. Second, non-live vaccines enhance the susceptibility of girls to unrelated infections. Third, the most recently administered vaccination has the strongest non-specific effects. Fourth, combinations of live and non-live vaccines given together have variable non-specific health effects. Fifth, vaccinating children with live vaccines in the presence of maternal immunity enhances beneficial non-specific effects and reduces mortality. Finally, vaccines might interact with other co-administered health interventions, for example vitamin A supplementation. The potential implications for child health are substantial. For example, if BCG vaccination was given to children at birth, if higher measles vaccination coverage could be obtained, if diphtheria, tetanus, and pertussis-containing vaccines were not given with or after measles vaccine, or if the BCG strain with the best non-specific effects could be used consistently, then child mortality could be considerably lower. Pursuing these emerging principles could improve our understanding and use of vaccines globally.

KW - Child

KW - Child Mortality

KW - Humans

KW - Vaccination

KW - Vaccines/administration & dosage

U2 - 10.1016/S1473-3099(19)30742-X

DO - 10.1016/S1473-3099(19)30742-X

M3 - Review

C2 - 32645296

VL - 20

SP - e274-e283

JO - The Lancet Infectious Diseases

JF - The Lancet Infectious Diseases

SN - 1473-3099

IS - 10

ER -

ID: 250077156