Evidence map›Paper›PMID 30818795›Full record

ReviewVaccines2019

Will Attention by Vaccine Developers to the Host's Nuclear Hormone Levels and Immunocompetence Improve Vaccine Success?

Robert E Sealy, Bart G Jones, Sherri L Surman, Rhiannon R Penkert, Stephane Pelletier, Geoff Neale, Julia L Hurwitz

Open access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Nuclear Receptors, Ligands and the Mammalian B Cell.International journal of molecular sciences · 2020
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

7 authors at 1 institution in 1 country.

Robert E SealyDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. bob.sealy@stjude.org.
Bart G JonesDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. bart.jones@stjude.org.
Sherri L SurmanDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. sherri.surman@stjude.org.
Rhiannon R PenkertDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. rhiannon.penkert@stjude.org.
Stephane PelletierDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. stephane.pelletier@stjude.org.
Geoff NealeThe Hartwell Center for Bioinformatics & Biotechnology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. geoffrey.neale@stjude.org.ORCID 0000-0003-3776-0858
Julia L HurwitzDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. julia.hurwitz@stjude.org.
St. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
American Lebanese Syrian Associated Charities ALSACNational Institutes of Health NCI P30 CA21765NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

Despite extraordinary advances in fields of immunology and infectious diseases, vaccine development remains a challenge. The development of a respiratory syncytial virus vaccine, for example, has spanned more than 50 years of research with studies of more than 100 vaccine candidates. Dozens of attractive vaccine products have entered clinical trials, but none have completed the path to licensing. Human immunodeficiency virus vaccine development has proven equally difficult, as there is no licensed product after more than 30 years of pre-clinical and clinical research. Here, we examine vaccine development with attention to the host. We discuss how nuclear hormones, including vitamins and sex hormones, can influence responses to vaccines. We show how nuclear hormones interact with regulatory elements of immunoglobulin gene loci and how the deletion of estrogen response elements from gene enhancers will alter patterns of antibody isotype expression. Based on these findings, and findings that nuclear hormone levels are often insufficient or deficient among individuals in both developed and developing countries, we suggest that failed vaccine studies may in some cases reflect weaknesses of the host rather than the product. We encourage analyses of nuclear hormone levels and immunocompetence among study participants in clinical trials to ensure the success of future vaccine programs.

Indexed as

antibody isotypesestrogenimmunoglobulin heavy chain locusnuclear hormonenuclear hormone receptorsresponse elementsvitamin Avitamin D

Identifiers

PMID30818795
PMCPMC6466149
OpenAlexW2917128889

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.