Evidence map›Paper›PMID 36823425›Full record

ArticleNPJ vaccines2023

Intranasal multivalent adenoviral-vectored vaccine protects against replicating and dormant M.tb in conventional and humanized mice.

Sam Afkhami, Michael R D'Agostino, Maryam Vaseghi-Shanjani, Madeleine Lepard, Jack X Yang, Rocky Lai, Margaret Wa Yan Choi, Alexis Chacon, Anna Zganiacz, Kees L M C Franken and 5 more

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Applications of humanized mice inMolecular medicine reports · 2026
    Review
  3. Article
  4. An adenoviral-vectored vaccine protects mice against aerosol challenge with Yersinia pestis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  5. Article
  6. Review
  7. Novel Multistage SubunitVaccines · 2025
    Article
  8. Experimental dissection of tuberculosis protective immunity: a human perspective.Frontiers in cellular and infection microbiology · 2025
    Review
  9. Article
  10. Article
  11. Humanized Mouse Models of Bacterial Infections.Antibiotics (Basel, Switzerland) · 2024
    Review
  12. Review
  13. Immunopathology of PulmonaryInternational journal of molecular sciences · 2024
    Article
  14. Article
  15. Review
  16. Review
  17. 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

15 authors at 4 institutions in 3 countries.

Sam AfkhamiMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Michael R D'AgostinoMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Maryam Vaseghi-ShanjaniMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Madeleine LepardMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Jack X YangMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Rocky LaiMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.ORCID http://orcid.org/0000-0002-3394-3086
Margaret Wa Yan ChoiMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Alexis ChaconMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Anna ZganiaczMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Kees L M C FrankenLeiden University Medical Centre, Leiden, The Netherlands.
Hildegund C ErtlThe Wistar Institute, Philadelphia, PA, USA.
Tom H M OttenhoffLeiden University Medical Centre, Leiden, The Netherlands.ORCID http://orcid.org/0000-0003-3706-3403
Mangalakumari JeyanathanMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Amy GillgrassMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada. gillgra@mcmaster.ca.ORCID http://orcid.org/0000-0002-6257-4013
Zhou XingMcMaster Immunology Research Centre, Department of Medicine, and Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada. xingz@mcmaster.ca.
McMaster University · CALeiden University Medical Center · NLMcMaster University Medical Centre · CAThe Wistar Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral-vectored vaccines are highly amenable for respiratory mucosal delivery as a means of inducing much-needed mucosal immunity at the point of pathogen entry. Unfortunately, current monovalent viral-vectored tuberculosis (TB) vaccine candidates have failed to demonstrate satisfactory clinical protective efficacy. As such, there is a need to develop next-generation viral-vectored TB vaccine strategies which incorporate both vaccine antigen design and delivery route. In this study, we have developed a trivalent chimpanzee adenoviral-vectored vaccine to provide protective immunity against pulmonary TB through targeting antigens linked to the three different growth phases (acute/chronic/dormancy) of Mycobacterium tuberculosis (M.tb) by expressing an acute replication-associated antigen, Ag85A, a chronically expressed virulence-associated antigen, TB10.4, and a dormancy/resuscitation-associated antigen, RpfB. Single-dose respiratory mucosal immunization with our trivalent vaccine induced robust, sustained tissue-resident multifunctional CD4

Identifiers

PMID36823425
PMCPMC9948798
OpenAlexW4321614596

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.