Evidence map›Paper›PMID 31948716›Full record

ReviewInternational journal of pediatric otorhinolaryngology2020

Panel 8: Vaccines and immunology.

Mark R Alderson, Tim Murphy, Stephen I Pelton, Laura A Novotny, Laura L Hammitt, Arwa Kurabi, Jian-Dong Li, Ruth B Thornton, Lea-Ann S Kirkham

Open access · greenAbstract readReview
In one paragraph

Review in International journal of pediatric otorhinolaryngology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Lipidation ofInfection and immunity · 2022
    Article
  5. Article
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

9 authors at 8 institutions in 2 countries.

Mark R AldersonPATH, Seattle, WA, USA. Electronic address: malderson@path.org.
Tim MurphyClinical and Translational Research Center, University at Buffalo, The State University of New York, Buffalo, NY, USA.
Stephen I PeltonBoston University School of Public Health, Boston University, Boston, MA, USA.
Laura A NovotnyThe Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Laura L HammittDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Arwa KurabiDivision of Otolaryngology, Department of Surgery, University of California, San Diego, CA, USA.
Jian-Dong LiCenter for Inflammation, Immunity & Infection, Institute for Biomedical Sciences, Georgia State University, GA, USA.
Ruth B ThorntonSchool of Biomedical Sciences, University of Western Australia, Australia and Wesfarmers Centre for Vaccines and Infectious Diseases Research, Telethon Kids Institute, Perth, Australia.
Lea-Ann S KirkhamWesfarmers Centre for Vaccines and Infectious Diseases Research, Telethon Kids Institute, Australia and Centre for Child Health Research, University of Western Australia, Perth, Australia.
The Kids Research Institute Australia · AUBoston University · USGeorgia State University · USJohns Hopkins University · USNationwide Children's Hospital · USProgram for Appropriate Technology in Health · USUniversity at Buffalo, State University of New York · USUniversity of California, San Diego · US

Funding

Middle ear responses in Otitis MediaR01DC000129 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RYAN, ALLEN F. · 1989 to 2021
$6.8M
Innovative therapy for diseases of the middle earR01DC012595 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RYAN, ALLEN F. · 2012 to 2023
$3.3M
Development of innovative therapeutics for otitis mediaR01DC015557 · NIDCD · GEORGIA STATE UNIVERSITY · PI KOHANE, DANIEL S, LI, JIAN-DONG · 2018 to 2022
$2.9M
Pathogenesis of pneumococcal otitis mediaR01DC013833 · NIDCD · GEORGIA STATE UNIVERSITY · PI LI, JIAN-DONG · 2015 to 2019
$1.6M
International Symposia on Recent Advances in Otitis MediaR13DC017389 · NIDCD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BAKALETZ, LAUREN O · 2018 to 2022
$91k
NIDCD NIH HHS R01 DC000129NIDCD NIH HHS R01 DC012595NIDCD NIH HHS R01 DC013833NIDCD NIH HHS R01 DC015557NIDCD NIH HHS R13 DC017389
6 · The paper itself

Abstract

objectiveTo review and highlight significant advances made towards vaccine development and understanding of the immunology of otitis media (OM) since the 19th International Symposium on Recent Advances in Otitis Media (ISOM) in 2015, as well as identify future research directions and knowledge gaps. DATA SOURCES: PubMed database, National Library of Medicine. REVIEW

methodsKey topics were assigned to each panel member for detailed review. Draft reviews were collated, circulated, and thoroughly discussed when the panel met at the 20th ISOM in June 2019. The final manuscript was prepared with input from all panel members.

conclusionsSince 2015 there have been a number of studies assessing the impact of licensed pneumococcal vaccines on OM. While these studies have confirmed that these vaccines are effective in preventing carriage and/or disease caused by vaccine serotypes, OM caused by non-vaccine serotype pneumococci and other otopathogens remains a significant health care burden globally. Development of multi-species vaccines is challenging but essential to reducing the global burden of OM. Influenza vaccination has been shown to prevent acute OM, and with novel vaccines against nontypeable Haemophilus influenzae (NTHi), Moraxella catarrhalis and Respiratory Syncytial Virus (RSV) in clinical trials, the potential to significantly prevent OM is within reach. Research into alternative vaccine delivery strategies has demonstrated the power of maternal and mucosal vaccination for OM prevention. Future OM vaccine trials must include molecular diagnostics of middle ear effusion, for detection of viruses and bacteria that are persisting in biofilms and to enable accurate assessment of vaccine impact on OM etiology. Understanding population differences in natural and vaccine-induced immune responses to otopathogens is also important for development of the most effective OM vaccines. Improved understanding of the interaction between otopathogens will also advance development of effective therapies and encourage the assessment of the indirect benefits of vaccination. IMPLICATIONS FOR PRACTICE: While NTHi and M. catarrhalis are the predominant otopathogens, funding opportunities to drive vaccine development for these species are limited due to a focus on prevention of childhood mortality rather than morbidity. Delivery of a comprehensive report on the high financial and social costs of OM, including the potential for OM vaccines to reduce antibiotic use and subsequent development of antimicrobial resistance (AMR), would likely assist in engaging stakeholders to recognize the value of prevention of OM and increase support for efforts on OM vaccine development. Vaccine trials with OM prevention as a clinical end-point are challenging, however a focus on developing assays that measure functional correlates of protection would facilitate OM vaccine development.

Indexed as

VaccinesBiofilmsHaemophilus VaccinesHumansInfluenza VaccinesMicrobial InteractionsMoraxellaceae InfectionsOtitis MediaOtitis Media with EffusionPneumococcal VaccinesRespiratory Syncytial Virus VaccinesSerogroupVaccinationHaemophilus VaccinesInfluenza VaccinesPneumococcal VaccinesRespiratory Syncytial Virus VaccinesVaccinesAdaptive immunityClinical trialInnate immun*Otitis media ANDVaccine

Identifiers

PMID31948716
PMCPMC7153269
OpenAlexW2995649881

What OpenQuestion holds

Textmetadata
LicenceTDM
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.