Evidence map›Paper›PMID 32210965›Full record

ReviewFrontiers in immunology2020

Advances in Developing CAR T-Cell Therapy for HIV Cure.

Jinxin Qi, Chengchao Ding, Xian Jiang, Yong Gao

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  3. Review
  4. Review
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  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Recent advances in CD8Heliyon · 2023
    Review
  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

4 authors at 3 institutions in 2 countries.

Jinxin QiDepartment of Dermatology, West China Hospital, Sichuan University, Chengdu, China.
Chengchao DingThe First Affiliated Hospital, Department of Life Science and Medicine, University of Science and Technology of China, Hefei, China.
Xian JiangDepartment of Dermatology, West China Hospital, Sichuan University, Chengdu, China.
Yong GaoDepartment of Microbiology and Immunology, The University of Western Ontario, London, ON, Canada.
West China Hospital of Sichuan University · CNUniversity of Science and Technology of China · CNWestern University · CA

Funding

CIHR OVV-152411
6 · The paper itself

Abstract

Acquired immune deficiency syndrome (AIDS), which is caused by HIV infection, is an epidemic disease that has killed millions of people in the last several decades. Although combination antiretroviral therapy (cART) has enabled tremendous progress in suppressing HIV replication, it fails to eliminate HIV latently infected cells, and infected individuals remain HIV positive for life. Lifelong antiretroviral therapy is required to maintain control of virus replication, which may result in significant problems, including long-term toxicity, high cost, and stigma. Therefore, novel therapeutic strategies are urgently needed to eliminate the viral reservoir in the host for HIV cure. In this review, we compare several potential strategies regarding HIV cure and focus on how we might utilize chimeric antigen receptor-modified T cells (CAR T) as a therapy to cure HIV infection.

Indexed as

Antiviral AgentsCD4-Positive T-LymphocytesHIV-1HIV InfectionsHumansImmunotherapy, AdoptiveReceptors, Chimeric AntigenVirus LatencyVirus ReplicationAntiviral AgentsReceptors, Chimeric Antigenacquired immune deficiency syndrome (AIDS)chimeric antigen receptor-modified T cell (CAR T)HIV cureHIV latent reservoirhuman immunodeficiency virus (HIV)immunotherapy

Identifiers

PMID32210965
PMCPMC7076163
OpenAlexW3011747051

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.