Evidence map›Paper›PMID 42685088›Full record

ArticlePloS one2026

Breakthrough infections and incomplete vaccine efficacy drive pathogen immune escape.

Minjin Kim, Eunha Shim

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Minjin KimDepartment of Mathematics, Soongsil University, Dongjak-gu, Seoul, Republic of Korea.ORCID https://orcid.org/0009-0004-2818-8583
Eunha ShimDepartment of Mathematics, Soongsil University, Dongjak-gu, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-3135-6360

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWhile vaccines effectively reduce disease severity and mortality, their consequences for pathogen immune escape remain poorly understood. Vaccines provide protection through three distinct mechanisms: prevention of infection, reduction of symptoms, and limitation of transmission. When vaccine efficacy is incomplete across multiple dimensions, breakthrough infections in vaccinated individuals may paradoxically increase pathogen escape pressure. This study investigates how vaccine efficacy profiles and coverage levels jointly affect escape pressure. MATERIALS AND

methodsWe developed a deterministic compartmental transmission model incorporating three distinct vaccine efficacy parameters: prevention of infection, reduction of symptoms, and limitation of transmission. The model quantifies differential contributions of symptomatic and asymptomatic infections in vaccinated and unvaccinated populations to immune escape pressure.

resultsInfection-blocking, symptom-blocking, and transmission-blocking immunity each reduced escape pressure, although no single component alone was sufficient to suppress escape pressure across most conditions. Combinations of efficacy components produced greater reductions. When vaccine efficacy was low across multiple components, increasing coverage could paradoxically elevate escape pressure above pre-vaccination levels. Even in a fully vaccinated population, escape pressure could exceed the pre-vaccination level when infection-blocking and symptom-blocking efficacy were simultaneously low. The effectiveness of symptom-blocking immunity depended on infection-blocking efficacy - when infection-blocking efficacy is low, symptom-blocking efficacy alone did not always suppress escape pressure below pre-vaccination levels. DISCUSSION: The effect of vaccination on immune escape depends on both vaccine efficacy profiles and coverage levels. Increasing vaccination coverage may increase rather than reduce escape pressure when efficacy is low across multiple dimensions. Combining efficacy across multiple dimensions produced greater reductions in escape pressure than relying on a single efficacy component.

Indexed as

Immune EvasionVaccine EfficacyBreakthrough InfectionsHumansUnvaccinated PersonsVaccination

Identifiers

PMID42685088
PMCPMC13537599

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Registered trials

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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.