Evidence map›Paper›PMID 37841838›Full record

ArticleResearch square2023

Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype.

Hongshuo Song, Manukumar Marichannegowda, Saini Setua, Meera Bose, Eric Sanders-Buell, David King, Michelle Zemil, Lindsay Wieczorek, Felisa Diaz-Mendez, Nicolas Chomont and 8 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. 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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Hongshuo SongUniversity of Maryland School of Medicine, Baltimore.
Manukumar MarichannegowdaUniversity of Maryland School of Medicine, Baltimore.
Saini SetuaUniversity of Maryland School of Medicine, Baltimore.
Meera Bose
Eric Sanders-BuellHenry M Jackson Foundation.
David KingThe Henry M. Jackson Foundation for the Advancement of Military Medicine.
Michelle ZemilU.S. Military HIV Research Program, Walter Reed Army Institute of Research.
Lindsay WieczorekU.S. Military HIV Research Program, Walter Reed Army Institute of Research.
Felisa Diaz-MendezUniversity of Maryland School of Medicine, Baltimore.
Nicolas ChomontUniversité de Montréal, Department of Microbiology, Infectiology and Immunology.ORCID 0000-0001-9747-5018
Rasmi ThomasU.S. Military HIV Research Program, Walter Reed Army Institute of Research.
Leilani FranciscoU.S. Military HIV Research Program, Walter Reed Army Institute of Research.
Leigh Anne EllerU.S. Military HIV Research Program, Walter Reed Army Institute of Research.
Victoria PolonisU.S. Military HIV Research Program, Walter Reed Army Institute of Research.
Sodsai TovanabutraMHRP-HJF.ORCID 0000-0002-5946-4227
Yutaka TagayaUniversity of Maryland School of Medicine, Baltimore.
Nelson MichaelCenter for Infectious Diseases Research, Walter Reed Army Institute of Research.
Merlin RobbU.S. Military HIV Research Program, Walter Reed Army Institute of Research; The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc.
University of Maryland, Baltimore · USWalter Reed Army Institute of Research · USHenry M. Jackson Foundation · USUniversité de Montréal · CA

Funding

Genetic imprints of therapeutic Ad26/MVA mosaic vaccine in rebound HIV-1 genome from acutely treated individualsR21AI147893 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SONG, HONGSHUO · 2019 to 2020
$441k
NIAID NIH HHS R21 AI147893
6 · The paper itself

Abstract

Nearly all transmitted/founder (T/F) HIV-1 are CCR5 (R5)-tropic. While previous evidence suggested that CXCR4 (X4)-tropic HIV-1 are transmissible, detection was not at the earliest stages of acute infection. Here, we identified an X4-tropic T/F HIV-1 in a participant in acute infection cohort. Coreceptor assays demonstrated that this T/F virus is strictly CXCR4 tropic. The participant experienced significantly faster CD4 depletion compared with R5 virus infected participants in the same cohort. Naïve and central memory CD4 subsets declined faster than effector and transitional memory subsets. All CD4 subsets, including naïve, were productively infected. Increased CD4

Identifiers

PMID37841838
PMCPMC10571614
OpenAlexW4387012311

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.