Evidence map›Paper›PMID 12481034›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Dynamics and selection of many-strain pathogens.

Julia R Gog, Bryan T Grenfell

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
5.5field-weighted citation impact, top 4% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

139 citing papers in PubMed, 321 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Understanding patterns of variant emergence and spread in an ongoing epidemic.medRxiv : the preprint server for health sciences · 2026
    Article
  6. Final-Size Solutions for SIRI Models with Vaccination.Bulletin of mathematical biology · 2026
    Article
  7. Article
  8. Article
  9. Concepts and Methods for Predicting Viral Evolution.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Article
  11. Concepts and methods for predicting viral evolution.bioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. A speed limit on serial strain replacement from original antigenic sin.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. A speed limit on serial strain replacement from original antigenic sin.bioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Article
  19. An immune memory-structured SIS epidemiological model for hyperdiverse pathogens.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Evolutionary stability of antigenically escaping viruses.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article

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

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Julia R GogDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, United Kingdom. julia@zoo.cam.ac.uk
Bryan T Grenfell
University of Cambridge · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Strain structure is of fundamental importance in the underlying dynamics of a number of pathogens. However, previous models have been too complex to accommodate many strains. This paper offers a solution to this problem, in the form of a simple model that is capable of capturing the dynamics of a large number of antigenic types that interact via host cross-immunity. We derive the structure of the model, which can manage the complexity of many strains by using a status-based formulation, assuming polarized immunity and cross-immunity act to reduced transmission probability. We then apply the model to address basic questions in strain dynamics, focusing particularly on the interpandemic dynamics of influenza. This model shows that strains have a tendency to "cluster." For a long infectious period, relative to host lifetime, clusters may coexist. By contrast, a short infectious period leads to a single dominant cluster at any given time. We show how the speed of cluster replacement depends on the specificity of cross-immunity and on the underlying pathogen mutation rate.

Indexed as

Models, BiologicalAntigenic VariationCluster AnalysisCross ReactionsImmunityMutationPopulation Dynamics

Identifiers

PMID12481034
PMCPMC139294
OpenAlexW1971707987

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.