Evidence map›Paper›PMID 35425270›Full record

ArticleRSC advances2022

Exploring divalent conjugates of 5-

Emil Johansson, Rémi Caraballo, Georg Zocher, Nitesh Mistry, Niklas Arnberg, Thilo Stehle, Mikael Elofsson

Abstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Emil JohanssonDepartment of Chemistry, Umeå University SE90187 Umeå Sweden mikael.elofsson@umu.se.
Rémi CaraballoDepartment of Chemistry, Umeå University SE90187 Umeå Sweden mikael.elofsson@umu.se.
Georg ZocherInterfaculty Institute of Biochemistry, University of Tübingen 72076 Tübingen Germany.
Nitesh MistryDepartment of Clinical Microbiology, Umeå University SE90185 Umeå Sweden.
Niklas ArnbergDepartment of Clinical Microbiology, Umeå University SE90185 Umeå Sweden.
Thilo StehleInterfaculty Institute of Biochemistry, University of Tübingen 72076 Tübingen Germany.
Mikael ElofssonDepartment of Chemistry, Umeå University SE90187 Umeå Sweden mikael.elofsson@umu.se.ORCID https://orcid.org/0000-0002-3219-4669

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coxsackievirus A24 variant (CVA24v) is responsible for several outbreaks and two pandemics of the highly contagious eye infection acute hemorrhagic conjunctivitis (AHC). Currently, neither prevention (vaccines) nor treatments (antivirals) are available for combating this disease. CVA24v attaches to cells by binding Neu5Ac-containing glycans on the surface of cells which facilitates entry. Previously, we have demonstrated that pentavalent Neu5Ac conjugates attenuate CVA24v infection of human corneal epithelial (HCE) cells. In this study, we report on the structure-based design of three classes of divalent Neu5Ac conjugates, with varying spacer lengths, and their effect on CVA24v transduction in HCE cells. In relative terms, the most efficient class of divalent Neu5Ac conjugates are more efficient than the pentavalent Neu5Ac conjugates previously reported.

Identifiers

PMID35425270
PMCPMC8979015

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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.