Evidence map›Paper›PMID 38793628›Full record

ReviewViruses2024

Models of Herpes Simplex Virus Latency.

Paige N Canova, Audra J Charron, David A Leib

Abstract readReview
In one paragraph

Review in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. HSV-1 as a Potential Driver of Alzheimer's Disease.Pathogens (Basel, Switzerland) · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  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

3 authors.

Paige N CanovaDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756, USA.ORCID 0000-0002-2269-773X
Audra J CharronGuarini School of Graduate and Advanced Studies at Dartmouth, Hanover, NH 03755, USA.ORCID 0009-0008-9472-5948
David A LeibGuarini School of Graduate and Advanced Studies at Dartmouth, Hanover, NH 03755, USA.ORCID 0000-0001-5539-8480

Funding

VIral and host mechanisms that tilt the HSV lytic/latent balanceP01AI098681 · NIAID · HARVARD MEDICAL SCHOOL · PI KNIPE, DAVID M. · 2013 to 2023
$19.2M
VIRAL & HOST FACTORS IN HERPETIC REACTIVATIONR01EY009083 · NEI · WASHINGTON UNIVERSITY · PI David A Leib · 1992 to 2026
$10.3M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
Understanding and optimizing antibody-based interventions against neonatal HSV infectionR01AI176646 · NIAID · DARTMOUTH COLLEGE · PI Margaret E Ackerman, David A Leib · 2023 to 2026
$3.1M
Does Antibody-Dependent Intracellular Neutralization Limit HSV-1 Reactivation?R21AI173941 · NIAID · DARTMOUTH COLLEGE · PI LEIB, DAVID A · 2023 to 2024
$451k
NEI NIH HHS R01 EY009083NIAID NIH HHS P01 AI098681NIAID NIH HHS R01 AI176646NIAID NIH HHS R21 AI173941NIAID NIH HHS T32 AI007363NIH HHS P01 AI098681NIH HHS R01 AI17664NIH HHS R01 EY09083NIH HHS R21 AI173941
6 · The paper itself

Abstract

Our current understanding of HSV latency is based on a variety of clinical observations, and in vivo, ex vivo, and in vitro model systems, each with unique advantages and drawbacks. The criteria for authentically modeling HSV latency include the ability to easily manipulate host genetics and biological pathways, as well as mimicking the immune response and viral pathogenesis in human infections. Although realistically modeling HSV latency is necessary when choosing a model, the cost, time requirement, ethical constraints, and reagent availability are also equally important. Presently, there remains a pressing need for in vivo models that more closely recapitulate human HSV infection. While the current in vivo, ex vivo, and in vitro models used to study HSV latency have limitations, they provide further insights that add to our understanding of latency. In vivo models have shed light on natural infection routes and the interplay between the host immune response and the virus during latency, while in vitro models have been invaluable in elucidating molecular pathways involved in latency. Below, we review the relative advantages and disadvantages of current HSV models and highlight insights gained through each.

Indexed as

Herpes SimplexVirus LatencyAnimalsDisease Models, AnimalHerpesvirus 1, HumanHumansSimplexvirusHSVin vivo and in vitro modelslatencyorganoidsreactivation

Identifiers

PMID38793628
PMCPMC11125678

What OpenQuestion holds

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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.