Evidence map›Paper›PMID 35572509›Full record

ReviewFrontiers in immunology2022

Evolving Strategies to Eliminate the CD4 T Cells HIV Viral Reservoir

Jarrod York, Kavitha Gowrishankar, Kenneth Micklethwaite, Sarah Palmer, Anthony L Cunningham, Najla Nasr

Open access · goldAbstract readReview
In one paragraph

Review 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 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Generation of Anti-HIV CAR-T Cells for Preclinical Research.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  12. Review
  13. Review
  14. Article
  15. Article
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

6 authors at 3 institutions in 1 country.

Jarrod YorkCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.
Kavitha GowrishankarCentre for Cancer Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.
Kenneth MicklethwaiteCentre for Cancer Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.
Sarah PalmerCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.
Anthony L CunninghamCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.
Najla NasrCentre for Virus Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.
The University of Sydney · AUWestmead Institute for Medical Research · AUSydney Children’s Hospitals Network · AU

Funding

Delaney AIDS Research Enterprise to Cure HIVUM1AI164560 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS, Sharon Ruth Lewin · 2021 to 2026
$32.0M
6 · The paper itself

Abstract

Although the advent of ART has significantly reduced the morbidity and mortality associated with HIV infection, the stable pool of HIV in latently infected cells requires lifelong treatment adherence, with the cessation of ART resulting in rapid reactivation of the virus and productive HIV infection. Therefore, these few cells containing replication-competent HIV, known as the latent HIV reservoir, act as the main barrier to immune clearance and HIV cure. While several strategies involving HIV silencing or its reactivation in latently infected cells for elimination by immune responses have been explored, exciting cell based immune therapies involving genetically engineered T cells expressing synthetic chimeric receptors (CAR T cells) are highly appealing and promising. CAR T cells, in contrast to endogenous cytotoxic T cells, can function independently of MHC to target HIV-infected cells, are efficacious and have demonstrated acceptable safety profiles and long-term persistence in peripheral blood. In this review, we present a comprehensive picture of the current efforts to target the HIV latent reservoir, with a focus on CAR T cell therapies. We highlight the current challenges and advances in this field, while discussing the importance of novel CAR designs in the efforts to find a HIV cure.

Indexed as

HIV-1HIV InfectionsCD4-Positive T-LymphocytesHumansImmunotherapy, AdoptiveVirus LatencyCD4CD8chimeric antigen receptorHIV-1latencyreactivation

Identifiers

PMID35572509
PMCPMC9098815
OpenAlexW4225101418

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.