Evidence map›Paper›PMID 36282589›Full record

ArticleThe Journal of clinical investigation2022

Human NK cells confer protection against HIV-1 infection in humanized mice.

Can M Sungur, Qiankun Wang, Ayşe N Ozantürk, Hongbo Gao, Aaron J Schmitz, Marina Cella, Wayne M Yokoyama, Liang Shan

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. CXCR6Frontiers in immunology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  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

8 authors at 2 institutions in 1 country.

Can M SungurDivision of Rheumatology, Department of Medicine.
Qiankun WangDivision of Infectious Diseases, Department of Medicine.
Ayşe N OzantürkDivision of Infectious Diseases, Department of Medicine.
Hongbo GaoDivision of Infectious Diseases, Department of Medicine.
Aaron J SchmitzDepartment of Pathology and Immunology, and.
Marina CellaDepartment of Pathology and Immunology, and.
Wayne M YokoyamaDivision of Rheumatology, Department of Medicine.
Liang ShanDivision of Infectious Diseases, Department of Medicine.
Office of Infectious Diseases · USCenter for Rheumatology · US

Funding

CRISPR for CureUM1AI164568 · NIAID · TEMPLE UNIV OF THE COMMONWEALTH · PI Tricia Helen Burdo, Kamel Khalili · 2021 to 2026
$27.7M
TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
Washington University Rheumatic DiseasesResearch Resource-based CenterP30AR073752 · NIAMS · WASHINGTON UNIVERSITY · PI Alfred Hyoungju Kim · 2018 to 2026
$7.6M
TRAINING IN THE IMMUNOLOGY OF RHEUMATIC DISEASEST32AR007279 · NIAMS · WASHINGTON UNIVERSITY · PI Megan Anne Cooper, Deborah J Lenschow · 1986 to 2026
$6.0M
Novel Strategies to Enhance Effector Cell Functions for Antibody-Mediated Clearance of HIV-1 InfectionR01AI155162 · NIAID · WASHINGTON UNIVERSITY · PI SHAN, LIANG · 2020 to 2024
$3.1M
DEVELOPING HUMANIZED MOUSE MODELS FOR THE STUDY OF HIV-1 LATENCY AND VIRAL EDUCATIONR00AI125065 · NIAID · WASHINGTON UNIVERSITY · PI SHAN, LIANG · 2018 to 2019
$498k
In vitro and in vivo analysis of macrophage-mediated clearance of HIV-1 latent reservoirR21AI143413 · NIAID · WASHINGTON UNIVERSITY · PI SHAN, LIANG · 2019 to 2020
$431k
NCI NIH HHS T32 CA009547NIAID NIH HHS R00 AI125065NIAID NIH HHS R01 AI155162NIAID NIH HHS R21 AI143413NIAID NIH HHS UM1 AI164568NIAMS NIH HHS P30 AR073752NIAMS NIH HHS T32 AR007279
6 · The paper itself

Abstract

The role of NK cells against HIV-1 infections remains to be elucidated in vivo. While humanized mouse models potentially could be used to directly evaluate human NK cell responses during HIV-1 infection, improved functional development of human NK cells in these hosts is needed. Here, we report the humanized MISTRG-6-15 mouse model, in which NK cells were quick to expand and exhibit degranulation, cytotoxicity, and proinflammatory cytokine production in nonlymphoid organs upon HIV-1 infection but had reduced functionality in lymphoid organs. Although HIV-1 infection induced functional impairment of NK cells, antiretroviral therapy reinvigorated NK cells in response to HIV-1 rebound after analytic treatment interruption. Moreover, a broadly neutralizing antibody, PGT121, enhanced NK cell function in vivo, consistent with antibody-dependent cellular cytotoxicity. Monoclonal antibody depletion of NK cells resulted in higher viral loads in multiple nonlymphoid organs. Overall, our results in humanized MISTRG-6-15 mice demonstrated that NK cells provided direct anti-HIV-1 responses in vivo but were limited in their responses in lymphoid organs.

Indexed as

HIV-1HIV InfectionsAnimalsAntibody-Dependent Cell CytotoxicityHumansKiller Cells, NaturalMiceViral LoadImmunologyNK cells

Identifiers

PMID36282589
PMCPMC9753998
OpenAlexW4307210428

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.