Evidence map›Paper›PMID 30281066›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2019

A Phase 2, Randomized, Control Trial of Group B Streptococcus (GBS) Type III Capsular Polysaccharide-tetanus Toxoid (GBS III-TT) Vaccine to Prevent Vaginal Colonization With GBS III.

Sharon L Hillier, Patricia Ferrieri, Morven S Edwards, Marian Ewell, Daron Ferris, Paul Fine, Vincent Carey, Leslie Meyn, Dakota Hoagland, Dennis L Kasper and 3 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00128219 (A Phase II Randomized, Double-Blinded, Comparative Clinical Trial for a Group B Streptococcus Serotype III-Tetanus Toxoid), which is not on this map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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.

NCT00128219 phase2completednot on this map

A Phase II Randomized, Double-Blinded, Comparative Clinical Trial for a Group B Streptococcus Serotype III-Tetanus Toxoid (GBS III-TT) Vaccine to Prevent Vaginal Acquisition of GBS Type III

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2003 to 2008Enrolled667ConditionsBeta Haemolytic Streptococcal InfectionArmsGBS III-TT, Tetanus and diptheria toxoids vaccine
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Neonatal Group B Streptococcus Disease.Pediatrics in review · 2024
    Review
  8. Vaccines forFrontiers in immunology · 2024
    Review
  9. Article
  10. Article
  11. Group BAntibiotics (Basel, Switzerland) · 2023
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. 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

13 authors at 9 institutions in 1 country.

Sharon L HillierUniversity of Pittsburgh School of Medicine, Magee-Womens Hospital, Pennsylvania.
Patricia FerrieriDepartment of Laboratory Medicine and Pathology and Pediatrics, University of Minnesota Medical School, Minneapolis.
Morven S EdwardsBaylor College of Medicine, Department of Pediatrics, Feigin Center, Houston, Texas.
Marian EwellThe EMMES Corporation, Rockville, Maryland.
Daron FerrisMedical College of Georgia, Augusta.
Paul FinePlanned Parenthood Gulf Coast, Houston, Texas.
Vincent CareyChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Leslie MeynUniversity of Pittsburgh School of Medicine, Magee-Womens Hospital, Pennsylvania.
Dakota HoaglandCOTA Enterprises, McLouth, Kansas.
Dennis L KasperDivision of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts.
Lawrence C PaolettiDivision of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts.
Heather HillThe EMMES Corporation, Rockville, Maryland.
Carol J BakerDivsion of Infectious Disease, Department of Pediatrics, University of Texas Health Science Center McGovern Medical School, Houston.
Emmes (United States) · USHarvard University · USMagee-Womens Hospital · USAugusta University · USBaylor College of Medicine · USBrigham and Women's Hospital · USPlanned Parenthood · USThe University of Texas Health Science Center at Houston · USUniversity of Minnesota Medical Center · US

Funding

PREVENTION OF GROUP B STREPTOCOCCAL (GBS) DISEASEN01AI25495 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · 2007 to 2008
$500k
NIAID NIH HHS N01AI25495
6 · The paper itself

Abstract

backgroundGroup B Streptococcus (GBS) frequently colonizes pregnant women and can cause sepsis and meningitis in young infants. If colonization was prevented through maternal immunization, a reduction in perinatal GBS disease might be possible. A GBS type III capsular polysaccharide (CPS)-tetanus toxoid conjugate (III-TT) vaccine was evaluated for safety and efficacy in preventing acquisition of GBS colonization.

methodsHealthy, nonpregnant women aged 18-40 years and screened to be GBS III vaginal and rectal culture negative were randomized to receive III-TT conjugate or tetanus diphtheria toxoid vaccine in a multicenter, observer-blinded trial. GBS vaginal and rectal cultures and blood were obtained bimonthly over 18 months. Serum concentrations of GBS III CPS-specific antibodies were determined using enzyme-linked immunosorbent assay.

resultsAmong 1525 women screened, 650 were eligible for the intent-to-treat analysis. For time to first acquisition of vaginal GBS III, vaccine efficacy was 36% (95% confidence interval [CI], 1%-58%; P = .044), and for first rectal acquisition efficacy was 43% (95% CI, 11% to 63%; P = .014). Two months post-immunization, geometric mean concentrations of serum GBS type III CPS-specific immunoglobulin G were 12.6 µg/mL (95% CI, 9.95 to 15.81) in GBS III-TT recipients, representing a 4-fold increase from baseline in 95% of women, which persisted. Both vaccines were well tolerated.

conclusionsGBS CPS III-TT conjugate vaccine significantly delayed acquisition of vaginal and rectal GBS III colonization. In addition to its use for maternal immunization to passively protect infants with maternally derived antibodies, a multivalent vaccine might also serve to reduce fetal and neonatal exposure to GBS. CLINICAL TRIALS REGISTRATION: NCT00128219.

Indexed as

AdultAntibodies, BacterialBacterial CapsulesFemaleHumansImmunogenicity, VaccineImmunoglobulin GOutcome Assessment, Health CareStreptococcal InfectionsStreptococcal VaccinesStreptococcus agalactiaeVaccinationVaccines, ConjugateVaginosis, BacterialYoung AdultAntibodies, Bacterialgroup B streptococcal type III capsular polysaccharide-tetanus toxoid vaccineImmunoglobulin GStreptococcal VaccinesVaccines, ConjugateGBSrectal colonizationvaccinevaginal colonization

Identifiers

PMID30281066
PMCPMC7317289
OpenAlexW2895481480

What OpenQuestion holds

Textmetadata
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.