Evidence map›Paper›PMID 21492929›Full record

ReviewLancet (London, England)2011

Serotype replacement in disease after pneumococcal vaccination.

Daniel M Weinberger, Richard Malley, Marc Lipsitch

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Lancet (London, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01735084 (Pneumococcal Conjugate Vaccine), which is not on this map. Cited by 537 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
537citing papers in PubMed, 7 pooled it
47.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01735084 phase4completednot on this mapstarted 2013, after this paper: background citation

Pneumococcal Conjugate Vaccine (PCV) Schedules for the Northern Territory (NT): Randomised Controlled Trial of Booster Vaccines to Broaden and Strengthen Protection From Invasive and Mucosal Infections.

TypeinterventionalSponsorMenzies School of Health ResearchRan2013 to 2019Enrolled261ConditionsOtitis Media, Febrile Illness, Cough, Lower Respiratory Tract InfectionArmsPrevenar13, Synflorix
3 · Its place in the literature

Who cites it

537 citing papers in PubMed, 7 syntheses or guidelines pooled it, 1,019 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. Trial
  9. Trial
  10. Article
  11. Effectiveness of the 10-valent pneumococcal non-typeableHuman vaccines & immunotherapeutics · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

477 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Daniel M WeinbergerDepartment of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA, USA. weinbergerdm@mail.nih.gov
Richard Malley
Marc Lipsitch
Boston Children's Hospital · USCenter for Disease Dynamics, Economics & Policy · USHarvard University · US

Funding

VACCINATION AND THE EVOLUTIONARY DYNAMICS OF PNEUMOCOCCIR01AI048935 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LIPSITCH, MARC · 2001 to 2016
$8.8M
Mechanisms of Immunity to Pneumococcal ColonizationR01AI066013 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI MALLEY, RICHARD · 2007 to 2011
$2.1M
NIAID NIH HHS R01 AI048935NIAID NIH HHS R01 AI066013
6 · The paper itself

Abstract

Vaccination with heptavalent pneumococcal conjugate vaccine (PCV7) has significantly reduced the burden of pneumococcal disease and has had an important public health benefit. Because this vaccine targets only seven of the more than 92 pneumococcal serotypes, concerns have been raised that non-vaccine serotypes (NVTs) could increase in prevalence and reduce the benefits of vaccination. Indeed, among asymptomatic carriers, the prevalence of NVTs has increased substantially, and consequently, there has been little or no net change in the bacterial carriage prevalence. In many populations, pneumococcal disease caused by NVT has increased, but in most cases this increase has been less than the increase in NVT carriage. We review the evidence for serotype replacement in carriage and disease, and address the surveillance biases that might affect these findings. We then discuss possible reasons for the discrepancy between near-complete replacement in carriage and partial replacement for disease, including differences in invasiveness between vaccine serotypes. We contend that the magnitude of serotype replacement in disease can be attributed, in part, to a combination of lower invasiveness of the replacing serotypes, biases in the pre-vaccine carriage data (unmasking), and biases in the disease surveillance systems that could underestimate the true amount of replacement. We conclude by discussing the future potential for serotype replacement in disease and the need for continuing surveillance.

Indexed as

SerotypingCarrier StateHeptavalent Pneumococcal Conjugate VaccineHumansPneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniaeHeptavalent Pneumococcal Conjugate VaccinePneumococcal Vaccines

Identifiers

PMID21492929
PMCPMC3256741
OpenAlexW2150562212

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.