Evidence map›Paper›PMID 40367245›Full record

ArticlePloS one2025

Modeling protective meningococcal antibody responses and factors influencing antibody persistence following vaccination with MenAfriVac using machine learning.

Md Nasir, William B Weeks, Shahrzad Gholami, Anthony Marfin, Mark Alderson, Troy Leader, Brian Taliesin, Rahul Dodhia, Juan Lavista Ferres, Niranjan Bhat

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Md NasirAI for Good Lab, Microsoft, Redmond, Washington, United States of America.ORCID https://orcid.org/0000-0002-3955-0996
William B WeeksAI for Good Lab, Microsoft, Redmond, Washington, United States of America.
Shahrzad GholamiAI for Good Lab, Microsoft, Redmond, Washington, United States of America.
Anthony MarfinCenter for Vaccine Innovation and Access, PATH, Seattle, Washington, United States of America.
Mark AldersonCenter for Vaccine Innovation and Access, PATH, Seattle, Washington, United States of America.
Troy LeaderCenter for Vaccine Innovation and Access, PATH, Seattle, Washington, United States of America.
Brian TaliesinCenter for Vaccine Innovation and Access, PATH, Seattle, Washington, United States of America.ORCID https://orcid.org/0009-0008-0474-4708
Rahul DodhiaAI for Good Lab, Microsoft, Redmond, Washington, United States of America.ORCID https://orcid.org/0000-0003-3812-3906
Juan Lavista FerresAI for Good Lab, Microsoft, Redmond, Washington, United States of America.
Niranjan BhatCenter for Vaccine Innovation and Access, PATH, Seattle, Washington, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meningococcal meningitis poses a significant public health burden in the meningitis belt region of sub-Saharan Africa. The introduction of the meningococcal PsA-TT vaccine (MenAfriVac®) has successfully eliminated Neisseria meningitidis serogroup A (NmA) cases in the region. However, the duration of post-vaccination immunity and the need for booster doses remain uncertain. To address this knowledge gap, we developed computational models using machine learning techniques to improve the effectiveness of modeling in guiding vaccination strategies for the African meningitis belt. Using serologic data from previous clinical trials of PsA-TT, we proposed a short-term and a long-term model that integrated demographic and medical variables (such as age, height and weight) with previous antibody titer levels and vaccination information to predict NmA antibody titer levels following vaccination. In the short-term model, we found moderately high performance (R-squared = 0.59) for out-of-training-data subjects and even better performance (R squared = 0.83) in the long-term evaluation. Our models estimated the half-life of the vaccine to be 13.9 years for the study population overall, similar to previously reported estimates. Machine learning techniques offer several advantages over previous approaches, as they do not require multiple readings from the same subject, can be rigorously validated using a subset of subject data not used for training. The proposed approach also facilitates the interpretation of the relationship between input variables and antibody levels at a population level. By incorporating subject-specific demographic and medical variables, our models could potentially be used to tailor vaccination schedules to at-risk populations.

Indexed as

Antibodies, BacterialAntibody FormationMachine LearningMeningitis, MeningococcalMeningococcal VaccinesAdolescentAdultChildChild, PreschoolFemaleHumansMaleVaccinationYoung AdultAntibodies, BacterialMenAfriVacMeningococcal Vaccines

Identifiers

PMID40367245
PMCPMC12077764

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.