Evidence map›Paper›PMID 30232277›Full record

ArticleJCI insight2018

Combination anti-PD-1 and antiretroviral therapy provides therapeutic benefit against SIV.

Geetha H Mylvaganam, Lynette S Chea, Gregory K Tharp, Sakeenah Hicks, Vijayakumar Velu, Smita S Iyer, Claire Deleage, Jacob D Estes, Steven E Bosinger, Gordon J Freeman and 2 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Dual Blockade of LILRB1 and LILRB2 Enhances Antiviral Immune Responses in SIV Infection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. An angel or a devil? Current view on the role of CD8Journal of translational medicine · 2024
    Review
  16. Review
  17. Article
  18. GITR activationiScience · 2023
    Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Geetha H MylvaganamDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Lynette S CheaDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Gregory K TharpDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Sakeenah HicksDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Vijayakumar VeluDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Smita S IyerDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Claire DeleageAIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, Maryland, USA.
Jacob D EstesAIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, Maryland, USA.
Steven E BosingerDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Gordon J FreemanDepartment of Medical Oncology and Cancer Vaccine Center, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Rafi AhmedDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Rama R AmaraDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Emory University · USLeidos (United States) · USDana-Farber Cancer Institute · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Carlos del Rio · 2002 to 2026
$74.0M
Viral Testing Core-Maintenance of the SPF Breeding Colonies at Yerkes National Primate Research CenterU42OD011023 · OD · EMORY UNIVERSITY · PI Matthew Ryan Gardner · 2018 to 2026
$17.5M
Targeting PD-1 Pathway for Functional Cure of AIDSR37AI112787 · NIAID · EMORY UNIVERSITY · PI AMARA, RAMA RAO · 2014 to 2023
$9.2M
PD-1 blockade as a therapy for SIV/AIDSR01AI074417 · NIAID · EMORY UNIVERSITY · PI AMARA, RAMA RAO · 2008 to 2010
$2.3M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENCRR NIH HHS P51 RR000165NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI074417NIAID NIH HHS R37 AI112787NIH HHS P51 OD011132NIH HHS U42 OD011023
6 · The paper itself

Abstract

Therapeutic strategies that augment antiviral immunity and reduce the viral reservoir are critical to achieving durable remission of HIV. The coinhibitory receptor programmed death-1 (PD-1) regulates CD8+ T cell dysfunction during chronic HIV and SIV infections. We previously demonstrated that in vivo blockade of PD-1 during chronic SIV infection improves the function of antiviral CD8+ T cells and B cells. Here, we tested the immunological and virological effects of PD-1 blockade combined with antiretroviral therapy (ART) in rhesus macaques. Administration of anti-PD-1 antibody 10 days prior to ART initiation rapidly enhanced antiviral CD8+ T cell function and diminished IFN-stimulated genes. This resulted in faster viral suppression in plasma and better Th17 cell reconstitution in the rectal mucosa following ART initiation. PD-1 blockade during ART resulted in lower levels of cell-associated replication-competent virus. Following ART interruption, PD-1 antibody-treated animals showed markedly higher expansion of proliferating CXCR5+perforin+granzyme B+ effector CD8+ T cells and lower regulatory T cells that resulted in better control of viremia. Our results show that PD-1 blockade can be administered safely with ART to augment antiviral CD8+ T cell function and reduce the viral reservoir, leading to improved control of viral rebound after ART interruption.

Indexed as

AnimalsAntibodies, MonoclonalAnti-Retroviral AgentsB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationCombined Modality TherapyDisease Models, AnimalGranzymesHIV-1HIV InfectionsImmunotherapyKi-67 AntigenMacaca mulattaProgrammed Cell Death 1 ReceptorAntibodies, MonoclonalAnti-Retroviral AgentsGranzymesKi-67 AntigenProgrammed Cell Death 1 ReceptorAIDS/HIVImmunologyImmunotherapy

Identifiers

PMID30232277
PMCPMC6237231
OpenAlexW2889604322

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.