Evidence map›Paper›PMID 36505432›Full record

ArticleFrontiers in immunology2022

HIV-1 infected humanized DRAGA mice develop HIV-specific antibodies despite lack of canonical germinal centers in secondary lymphoid tissues.

Matthew T Ollerton, Joy M Folkvord, Kristina K Peachman, Soumya Shashikumar, Elaine B Morrison, Linda L Jagodzinski, Sheila A Peel, Mohammad Khreiss, Richard T D'Aquila, Sofia Casares and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 25% 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.

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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. 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

12 authors at 4 institutions in 1 country.

Matthew T OllertonDepartment of Medicine, University of Arizona, Tucson, AZ, United States.
Joy M FolkvordDepartment of Medicine, University of Arizona, Tucson, AZ, United States.
Kristina K PeachmanLaboratory of Adjuvant and Antigen Research, United States Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Soumya ShashikumarUS Military Malaria Vaccine Program, Naval Medical Research Center, Silver Spring, MD, United States.
Elaine B MorrisonLaboratory of Adjuvant and Antigen Research, United States Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Linda L JagodzinskiDiagnostics and Countermeasure Branch, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Sheila A PeelDiagnostics and Countermeasure Branch, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Mohammad KhreissDepartment of Surgery, University of Arizona, Tucson, AZ, United States.
Richard T D'AquilaDepartment of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
Sofia CasaresUS Military Malaria Vaccine Program, Naval Medical Research Center, Silver Spring, MD, United States.
Mangala RaoLaboratory of Adjuvant and Antigen Research, United States Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Elizabeth ConnickDepartment of Medicine, University of Arizona, Tucson, AZ, United States.
Walter Reed Army Institute of Research · USUniversity of Arizona · USNaval Medical Research Command · USNorthwestern University · US

Funding

Pathogenesis of Rebound SIV/HIV Viremia after Antiretrovral TherapyP01AI131346 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2017 to 2021
$8.0M
NIAID NIH HHS P01 AI131346
6 · The paper itself

Abstract

A major barrier in the use of humanized mice as models of HIV-1 (HIV) infection is the inadequate generation of virus-specific antibody responses. Humanized DRAGA (hDRAGA) mice generate antigen-specific class switched antibodies to several pathogens, but whether they do so in HIV infection and the extent to which their secondary lymphoid tissues (sLT) support germinal center responses is unknown. hDRAGA mice were evaluated for their ability to support HIV replication, generate virus-specific antibody responses, develop splenocyte subsets, and organize sLT architecture. hDRAGA mice supported persistent HIV replication and developed modest levels of gp41-specific human IgM and IgG. Spleens from uninfected and HIV infected hDRAGA mice contained differentiated B and CD4

Indexed as

HIV-1HIV InfectionsAnimalsCD8-Positive T-LymphocytesGerminal CenterHIV AntibodiesMiceHIV Antibodiesfolliclegerminal center (GC)HIV - human immunodeficiency virushumanized DRAGA micesecondary lymphoid tissue

Identifiers

PMID36505432
PMCPMC9732419
OpenAlexW4310040230

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.