Evidence map›Paper›PMID 39441011›Full record

ArticlemSphere2024

A whole-cell pertussis vaccine engineered to elicit reduced reactogenicity protects baboons against pertussis challenge.

Parul Kapil, Yihui Wang, Kelsey Gregg, Lindsey Zimmerman, Damaris Molano, Jonatan Maldonado Villeda, Peter Sebo, Tod J Merkel

Abstract read
In one paragraph

Article in mSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

8 authors.

Parul Kapil *Center for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.
Yihui Wang *Center for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.ORCID 0000-0002-7718-3816
Kelsey GreggCenter for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.ORCID 0000-0002-1483-735X
Lindsey ZimmermanCenter for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.
Damaris MolanoCenter for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.
Jonatan Maldonado VilledaCenter for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.
Peter SeboInstitute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0002-9755-7715
Tod J MerkelCenter for Biologics Evaluation and Research, FDA, Bethesda, Maryland, USA.ORCID 0009-0007-3296-9202

Funding

Food and Drug Administration and by the National Institutes of Health Division of Microbiology and Infectious Disease AAI14017-001-00002HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AAI14017-001-00002National Institute of Virology and Microbiology Programme EXCELES ID Project No. LX22NPO5103
6 · The paper itself

Abstract

Whole-cell pertussis (wP) vaccines introduced in the 1940s led to a dramatic reduction of pertussis incidence and are still widely used in low- and middle-income countries (LMICs) worldwide. The reactogenicity of wP vaccines resulted in reduced public acceptance, which drove the development and introduction of acellular pertussis (aP) vaccines in high-income countries in the 1990s. Increased incidence of pertussis disease has been observed in high-income countries following the introduction of aP vaccines despite near universal rates of pediatric vaccination. These increases are attributed to the reduced protection against colonization, carriage, and transmission as well as reduced duration of immunity conferred by aP vaccines relative to the wP vaccines they replaced. A reduced reactogenicity whole-cell pertussis (RRwP) vaccine was recently developed with the goal of achieving the same protection as conferred by wP vaccination but with an improved safety profile, which may benefit countries in which wP vaccines are still in routine use. In this study, we tested the RRwP vaccine in a baboon model of pertussis infection. We found that the RRwP vaccine induced comparable cellular and humoral immune responses and comparable protection following challenge relative to the wP vaccine, while significantly reducing injection-site reactogenicity.IMPORTANCEThe World Health Organization (WHO) recommended in 2015 that countries administering wP vaccines in their national vaccine programs should continue to do so, and that switching to aP vaccines for primary infant immunization should only be considered if periodic booster vaccinations and/or maternal immunization could be assured and sustained in their national immunization schedules (WHO, Vaccine 34:1423-1425, 2016, https://doi.org/10.1016/j.vaccine.2015.10.136). Due to the considerably higher cost of aP vaccines and the larger number of doses required, most LMICs continue to use wP vaccines. The development and introduction of a wP vaccine that induces fewer adverse events without sacrificing protection would significantly benefit countries in which wP vaccines are still in routine use. The results of this study indicate this desirable goal may be achievable.

Indexed as

PapioPertussis VaccineWhooping CoughAnimalsAntibodies, BacterialBordetella pertussisDisease Models, AnimalFemaleMaleVaccinationAntibodies, BacterialPertussis Vaccinebaboon modelpertussiswhole cell vaccines

Identifiers

PMID39441011
PMCPMC11580402

What OpenQuestion holds

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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.