Evidence map›Paper›PMID 22234266›Full record

ArticleVaccine2012

Evaluation of Lassa virus vaccine immunogenicity in a CBA/J-ML29 mouse model.

Marco A Goicochea, Juan C Zapata, Joseph Bryant, Harry Davis, Maria S Salvato, Igor S Lukashevich

Abstract read
In one paragraph

Article in Vaccine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

29 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Lassa Virus Countermeasures.Current topics in microbiology and immunology · 2023
    Article
  6. Article
  7. Article
  8. Viruses · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Pre-clinical development of a vaccine against Lassa fever.Canada communicable disease report = Releve des maladies transmissibles au Canada · 2018
    Article
  20. 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

6 authors at 2 institutions in 2 countries.

Marco A GoicocheaInstitute of Human Virology, University of Maryland, School of Medicine, Baltimore, MD 21201, United States. mgoic001@umaryland.edu
Juan C Zapata
Joseph Bryant
Harry Davis
Maria S Salvato
Igor S Lukashevich
University of Maryland, Baltimore · USUniversity of Louisville · US

Funding

Development of New Bivalent Cross-Protective Arenaviral VaccinesR01AI093450 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI LUKASHEVICH, IGOR S., PUSHKO, PETER M. · 2011 to 2015
$3.9M
MOP/LAS chimeric vaccine against Lassa feverR01AI052367 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI LUKASHEVICH, IGOR S. · 2004 to 2007
$1.6M
Mopeia/Lassa Virus Reassortants as Lassa Fever VaccinesR21AI052367 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI LUKASHEVICH, IGOR S. · 2002 to 2002
$399k
Evaluation of LASV Protective Immunity in Mice Using Reassortant Virus ML29F31AI082993 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI GOICOCHEA, MARCO AURELIO · 2009 to 2010
$57k
NIAID NIH HHS AI052367NIAID NIH HHS AI093450NIAID NIH HHS F31 AI082993NIAID NIH HHS R01 AI052367NIAID NIH HHS R01 AI093450NIAID NIH HHS R21 AI052367
6 · The paper itself

Abstract

Lassa fever (LF) is one of the most prevalent viral hemorrhagic fevers in West Africa responsible for thousands of deaths annually. The BSL-4 containment requirement and lack of small animal model to evaluate Lassa virus (LASV)-specific cell-mediated immunity (CMI) complicate development of effective LF vaccines. Here we have described a CBA/J-ML29 model allowing evaluation of LASV-specific CMI responses in mice. This model is based on Mopeia virus reassortant clone ML29, an attractive immunogenic surrogate for LASV. A single intraperitoneal (i.p.) immunization of CBA/J mice with ML29 protected animals against a lethal homologous intracerebral (i.c.) challenge with 588 LD(50). The ML29-immunized mice displayed negligible levels of LASV-specific antibody titers, but LASV-specific CMI responses were detectable early and peaked on day 8-10 after immunization. A T cell cytotoxicity assay in vivo showed a correlation between LASV-specific cytotoxicity and the timing of protection induced by the ML29 immunization. Notably, CBA/J mice that received CD8+ T cell-depleted splenocytes from ML29-immunized donors all succumbed to a lethal i.c. challenge, demonstrating that CD8+ T cells are critical in protection. The CBA/J-ML29 model can be useful immunological tool for the preliminary evaluation of immunogenicity and efficacy of vaccine candidates against LASV outside of BSL-4 containment facilities.

Indexed as

AnimalsAntibodies, ViralArenaviruses, Old WorldDisease Models, AnimalInjections, IntraperitonealLassa FeverLymphocyte DepletionMiceMice, Inbred CBAReassortant VirusesSurvival AnalysisT-Lymphocytes, CytotoxicViral VaccinesAntibodies, ViralViral Vaccines

Identifiers

PMID22234266
PMCPMC3562134
OpenAlexW1998709015

What OpenQuestion holds

Textmetadata
LicenceTDM
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.