Evidence map›Paper›PMID 28520969›Full record

ReviewThe Journal of infectious diseases2017

Cell-Mediated Immunity to Target the Persistent Human Immunodeficiency Virus Reservoir.

James L Riley, Luis J Montaner

Abstract readReview
In one paragraph

Review in The Journal of infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Cell therapies for viral diseases: a new frontier.Seminars in immunopathology · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. HIV-1 latency reversal agent boosting is not limited by opioid use.medRxiv : the preprint server for health sciences · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Harnessing CD8Frontiers in immunology · 2019
    Review
  20. 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

2 authors.

James L RileyDepartment of Microbiology and Center for Cellular Immunotherapies, University of Pennsylvania, and.
Luis J MontanerHIV-1 Immunopathogenesis Laboratory, Wistar Institute, Philadelphia, Pennsylvania.

Funding

First-in-human study of two anti-SARS CoV-2 antibodies in health volunteersUM1AI126620 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J, RILEY, JAMES L. · 2016 to 2021
$24.5M
Lentivirus-based Immunogene Therapy for HIV InfectionU19AI066290 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI JUNE, CARL H. · 2005 to 2009
$7.2M
Targeting the Persistent HIV-1 Viral Reservoir Using Engineered T cellsR33AI104280 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI RILEY, JAMES L. · 2015 to 2017
$1.4M
Targeting the Persistent HIV-1 Viral Reservoir Using Engineered T cellsR21AI104280 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI RILEY, JAMES L. · 2013 to 2014
$437k
6 · The paper itself

Abstract

Effective clearance of virally infected cells requires the sequential activity of innate and adaptive immunity effectors. In human immunodeficiency virus (HIV) infection, naturally induced cell-mediated immune responses rarely eradicate infection. However, optimized immune responses could potentially be leveraged in HIV cure efforts if epitope escape and lack of sustained effector memory responses were to be addressed. Here we review leading HIV cure strategies that harness cell-mediated control against HIV in stably suppressed antiretroviral-treated subjects. We focus on strategies that may maximize target recognition and eradication by the sequential activation of a reconstituted immune system, together with delivery of optimal T-cell responses that can eliminate the reservoir and serve as means to maintain control of HIV spread in the absence of antiretroviral therapy (ART). As evidenced by the evolution of ART, we argue that a combination of immune-based strategies will be a superior path to cell-mediated HIV control and eradication. Available data from several human pilot trials already identify target strategies that may maximize antiviral pressure by joining innate and engineered T cell responses toward testing for sustained HIV remission and/or cure.

Indexed as

Immunity, CellularClinical Trials as TopicHIVHIV InfectionsHumansImmunotherapyCARCCR5Gene therapyIFN-α.NK

Identifiers

PMID28520969
PMCPMC5853458

What OpenQuestion holds

Textmetadata
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.