Evidence map›Paper›PMID 37885158›Full record

ReviewHuman vaccines & immunotherapeutics2023

Using the power of innate immunoprofiling to understand vaccine design, infection, and immunity.

Jennifer Connors, Gina Cusimano, Nathan Mege, Kyra Woloszczuk, Emily Konopka, Matthew Bell, David Joyner, Jennifer Marcy, Virginie Tardif, Michele A Kutzler and 2 more

Abstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. 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

12 authors.

Jennifer ConnorsDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0001-9137-0717
Gina CusimanoDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0002-1393-9485
Nathan MegeTower Health, Reading Hospital, West Reading, PA, USA.ORCID 0000-0003-4564-7433
Kyra WoloszczukDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.
Emily KonopkaDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.
Matthew BellDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0001-7246-4021
David JoynerDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.
Jennifer MarcyDepartment of Molecular and Cellular Biology, Drexel University College of Medicine, Philadelphia, PA, USA.
Virginie TardifDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0001-5604-6524
Michele A KutzlerDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0001-5692-5617
Roshell MuirDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0003-2226-7825
Elias K HaddadDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0001-6924-4300

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the field of immunology, a systems biology approach is crucial to understanding the immune response to infection and vaccination considering the complex interplay between genetic, epigenetic, and environmental factors. Significant progress has been made in understanding the innate immune response, including cell players and critical signaling pathways, but many questions remain unanswered, including how the innate immune response dictates host/pathogen responses and responses to vaccines. To complicate things further, it is becoming increasingly clear that the innate immune response is not a linear pathway but is formed from complex networks and interactions. To further our understanding of the crosstalk and complexities, systems-level analyses and expanded experimental technologies are now needed. In this review, we discuss the most recent immunoprofiling techniques and discuss systems approaches to studying the global innate immune landscape which will inform on the development of personalized medicine and innovative vaccine strategies.

Indexed as

VaccinesImmunity, InnateSystems BiologyVaccinationVaccinesbioinformaticsCyTOFGWASinfectious diseaseinnate immune cellsinnate immune profilingluminexmesoscalemetabolomicsMIBImulti-color flow cytometrymultiplex cytokine profilingO-Linkphospho-flowRNA sequencingSystems immunologyvaccinology

Identifiers

PMID37885158
PMCPMC10760375

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.