Evidence map›Paper›PMID 34153005›Full record

ArticleThe Journal of clinical investigation2021

Cytomegalovirus mediates expansion of IL-15-responsive innate-memory cells with SIV killing function.

Gema Méndez-Lagares, Ning Chin, W L William Chang, Jaewon Lee, Míriam Rosás-Umbert, Hung T Kieu, David Merriam, Wenze Lu, Sungjin Kim, Lourdes Adamson and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Functional genomic analysis of the 68-1 RhCMV-Frontiers in immunology · 2024
    Article
  8. Article
  9. HIV T-cell immunogen design and delivery.Current opinion in HIV and AIDS · 2022
    Review
  10. Article
  11. Heterogeneity of circulating CD4Scientific reports · 2022
    Article
  12. Translational Utility of the Nonhuman Primate Model.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2022
    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

14 authors at 5 institutions in 2 countries.

Gema Méndez-LagaresCalifornia National Primate Research Center.
Ning ChinCalifornia National Primate Research Center.
W L William ChangCalifornia National Primate Research Center.
Jaewon LeeGraduate Group in Immunology, and.
Míriam Rosás-UmbertIrsiCaixa - AIDS Research Institute, Badalona, Barcelona, Spain.
Hung T KieuCalifornia National Primate Research Center.
David MerriamCalifornia National Primate Research Center.
Wenze LuCalifornia National Primate Research Center.
Sungjin KimDepartment of Medical Microbiology and Immunology.
Lourdes AdamsonCenter for Immunology and Infectious Diseases, University of California Davis, Davis, California, USA.
Christian BranderIrsiCaixa - AIDS Research Institute, Badalona, Barcelona, Spain.
Paul A LuciwCalifornia National Primate Research Center.
Peter A BarryCalifornia National Primate Research Center.
Dennis J Hartigan-O'ConnorCalifornia National Primate Research Center.
Oregon National Primate Research Center · USUniversity of California, Davis · USIrsiCaixa · ESUniversitat de Vic - Universitat Central de Catalunya · ESUniversity of California, San Francisco · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALLORY O JOHNSON · 1988 to 2026
$93.6M
UC Davis Biostatistics CoreP01AI131568 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI STEVENSON, MARIO · 2017 to 2021
$7.1M
Improved RhCMV/SIV vaccine efficacy via IL-10 pathway modulationR01AI143554 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HARTIGAN-O'CONNOR, DENNIS J. · 2018 to 2022
$4.5M
Reservoir depletion and anti-retroviral therapy for infant functional cureR01AI118451 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HARTIGAN-O'CONNOR, DENNIS J. · 2015 to 2019
$4.2M
Effective CMV-based SIV vaccine regimens for newborn infants via IL-10 modulationR01AI150554 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HARTIGAN-O'CONNOR, DENNIS J. · 2020 to 2023
$3.0M
Acquisition of Covaris E220 and Sciclone G3 systems for high throughput sequencinS10OD010786 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COMAI, LUCA · 2012 to 2012
$311k
NIAID NIH HHS P01 AI131568NIAID NIH HHS P30 AI027763NIAID NIH HHS R01 AI118451NIAID NIH HHS R01 AI143554NIAID NIH HHS R01 AI150554NIH HHS P51 OD011107NIH HHS S10 OD010786
6 · The paper itself

Abstract

Interindividual immune variability is driven predominantly by environmental factors, including exposure to chronic infectious agents such as cytomegalovirus (CMV). We investigated the effects of rhesus CMV (RhCMV) on composition and function of the immune system in young macaques. Within months of infection, RhCMV was associated with impressive changes in antigen presenting cells, T cells, and NK cells-and marked expansion of innate-memory CD8+ T cells. These cells express high levels of NKG2A/C and the IL-2 and IL-15 receptor beta chain, CD122. IL-15 was sufficient to drive differentiation of the cells in vitro and in vivo. Expanded NKG2A/C+CD122+CD8+ T cells in RhCMV-infected macaques, but not their NKG2-negative counterparts, were endowed with cytotoxicity against class I-deficient K562 targets and prompt IFN-γ production in response to stimulation with IL-12 and IL-18. Because RhCMV clone 68-1 forms the viral backbone of RhCMV-vectored SIV vaccines, we also investigated immune changes following administration of RhCMV 68-1-vectored SIV vaccines. These vaccines led to impressive expansion of NKG2A/C+CD8+ T cells with capacity to inhibit SIV replication ex vivo. Thus, CMV infection and CMV-vectored vaccination drive expansion of functional innate-like CD8 cells via host IL-15 production, suggesting that innate-memory expansion could be achieved by other vaccine platforms expressing IL-15.

Indexed as

Immunity, InnateImmunologic MemoryAnimalsCD8-Positive T-LymphocytesCytomegalovirusFemaleInterleukin-15Killer Cells, NaturalMacaca mulattaMaleSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusInterleukin-15Cellular immune responseImmunologyInfectious diseaseInnate immunityT cells

Identifiers

PMID34153005
PMCPMC8321572
OpenAlexW3175975623

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.