Evidence map›Paper›PMID 27756530›Full record

ReviewTrends in molecular medicine2016

Modulating Antibody Functionality in Infectious Disease and Vaccination.

Bronwyn M Gunn, Galit Alter

Registry-linked trialAbstract readReview
In one paragraph

Review in Trends in molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05856396 (Maternal Determinants of Infant Immunity to Pertussis), which is not on this map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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.

NCT05856396 phase4completednot on this mapstarted 2023, after this paper: background citation

Maternal Determinants of Infant Immunity to Pertussis

TypeinterventionalSponsorCentre Hospitalier Universitaire Saint PierreRan2023 to 2025Enrolled200ConditionsVaccination, Infection, Maternal-Fetal Relations, PertussisArmsTriaxis® (Pertussis-containing vaccine), Vaxelis® (Pertussis-containing vaccine)
3 · Its place in the literature

Who cites it

53 citing papers in PubMed.

  1. Trial
  2. IgA and IgG1 Specific to Vi Polysaccharide ofFrontiers in immunology · 2019
    Trial
  3. Latently and uninfected healthcare workers exposed to TB make protective antibodies againstProceedings of the National Academy of Sciences of the United States of America · 2017
    Trial
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Mapping Epitopes by Phage Display.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  18. Review
  19. Antibody glycosylation in COVID-19.Glycoconjugate journal · 2022
    Review
  20. 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

2 authors.

Bronwyn M GunnRagon Institute of MGH, MIT, and Harvard, Cambridge, MA 02139, USA.
Galit AlterRagon Institute of MGH, MIT, and Harvard, Cambridge, MA 02139, USA. Electronic address: galter@mgh.harvard.edu.

Funding

Demystifying the antiviral activity of the IgG3+ antibody responseR37AI080289 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ALTER, GALIT · 2015 to 2022
$5.8M
Tuning Fc-effector functions of HIV-specific antibodiesR01AI102660 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ALTER, GALIT · 2012 to 2015
$3.0M
Enhancing mucosal protection through antibody interactions with mucin proteinsF32AI114406 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI GUNN, BRONWYN MEI · 2014 to 2015
$106k
NIAID NIH HHS F32 AI114406NIAID NIH HHS R01 AI102660NIAID NIH HHS R37 AI080289
6 · The paper itself

Abstract

Induction of pathogen-specific binding antibodies has long been considered a signature of protective immunity following vaccination and infection. The humoral immune response is a complex network of antibodies that target different specificities and drive different functions, collectively acting to limit and clear infection either directly, via pathogen neutralization, or indirectly, via pathogen clearance by the innate immune system. Emerging data suggest that not all antibody responses are equal, and qualitative features of antibodies may be key to defining protective immune profiles. Here, we review the most recent advances in our understanding of protective functional antibody responses in natural infection, vaccination, and monoclonal antibody therapeutics. Moreover, we highlight opportunities to augment or modulate antibody-mediated protection through enhancement of antibody functionality.

Indexed as

Immunity, HumoralImmunity, InnateAnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibody AffinityCommunicable Disease ControlCommunicable DiseasesHumansVaccinationAntibodies, MonoclonalAntibodies, NeutralizingADCCantibodiesantibody glycosylationFc receptorsHIVvaccination

Identifiers

PMID27756530
PMCPMC8767654

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.