Evidence map›Paper›PMID 39450141›Full record

ArticleInfectious microbes & diseases2021

Site-Specific Conjugation of Cell Wall Polyrhamnose to Protein SpyAD Envisioning a Safe Universal Group A Streptococcal Vaccine.

Nina J Gao, Satoshi Uchiyama, Lucy Pill, Samira Dahesh, Joshua Olson, Leslie Bautista, Shilpa Maroju, Aym Berges, Janet Z Liu, Raymond H Zurich and 4 more

Abstract read
In one paragraph

Article in Infectious microbes & diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 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

14 authors.

Nina J GaoDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.
Satoshi UchiyamaDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.
Lucy PillVaxcyte, Inc., Foster City, CA 94404, USA.
Samira DaheshDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.
Joshua OlsonDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.
Leslie BautistaVaxcyte, Inc., Foster City, CA 94404, USA.
Shilpa MarojuVaxcyte, Inc., Foster City, CA 94404, USA.
Aym BergesVaxcyte, Inc., Foster City, CA 94404, USA.
Janet Z LiuDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.
Raymond H ZurichDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.
Nina van SorgeDepartment of Medical Microbiology and Infection Prevention, Amsterdam University Medical Center, Amsterdam, Netherlands.
Jeff FairmanVaxcyte, Inc., Foster City, CA 94404, USA.
Neeraj KapoorVaxcyte, Inc., Foster City, CA 94404, USA.
Victor NizetDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, UC San Diego, La Jolla, CA 92093, USA.

Funding

Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
GAS Switch from Colonizing Bacterium to Invasive PathogenR01AI077780 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NIZET, VICTOR · 2008 to 2019
$3.8M
Mechanisms of the M protein in group A Streptococcus virulenceR01AI096837 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PARTHO, NIZET, VICTOR · 2011 to 2015
$2.7M
Broad recognition of group A Streptococcus M proteinsR21AI140436 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PARTHO, NIZET, VICTOR · 2018 to 2019
$426k
NIAID NIH HHS R01 AI077780NIAID NIH HHS R01 AI096837NIAID NIH HHS R21 AI140436NIGMS NIH HHS T32 GM008666
6 · The paper itself

Abstract

Development of an effective vaccine against the leading human bacterial pathogen group A Streptococcus (GAS) is a public health priority. The species defining group A cell wall carbohydrate (GAC, Lancefield antigen) can be engineered to remove its immunodominant N-acetylglucosamine (GlcNAc) side chain, implicated in provoking autoimmune cross-reactivity in rheumatic heart disease, leaving its polyrhamnose core (GAC

Indexed as

bacterial infectionclick chemistryconjugate vaccineGroup A carbohydrateGroup A StreptococcusLancefield antigennon-natural amino acidsSpyADStreptococcus pyogenesXpressCF™

Identifiers

PMID39450141
PMCPMC11501091

What OpenQuestion holds

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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.