Evidence map›Paper›PMID 28435678›Full record

ArticleClinical & translational immunology2017

Screening for immune response against Dengue virus in Vietnamese non-human primates: implications for vaccine developers.

Laura Lazo Vázquez, Edith Suzarte Portal, Jorge Castro Velazco, Phuong Yen, Le Trung Dung, Lázaro Gil González, Iris Valdés Prado, Ernesto Marcos López, Karem Cobas Acosta, Nguyen Dang Hien and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

12 authors at 2 institutions in 2 countries.

Laura Lazo VázquezVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Edith Suzarte PortalVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Jorge Castro VelazcoVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Phuong YenThe Center for Research and Production of Vaccines and Biological-POLYVAC, Hanoi, Vietnam.
Le Trung DungThe Center for Research and Production of Vaccines and Biological-POLYVAC, Hanoi, Vietnam.
Lázaro Gil GonzálezVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Iris Valdés PradoVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Ernesto Marcos LópezVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Karem Cobas AcostaVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Nguyen Dang HienThe Center for Research and Production of Vaccines and Biological-POLYVAC, Hanoi, Vietnam.
Gerardo Guillén NietoVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Lisset Hermida CruzVaccines Department, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Centro de Ingeniería Genética y Biotecnología · CUNational Institute for Control of Vaccines and Biologicals · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the major problems faced for the development of a vaccine against Dengue virus is the lack of a suitable animal model. Although non-human primates do not show overt signs of disease, these animals develop viremia after the infection and are the best model to evaluate vaccine candidates against this pathogen. However, for that purpose, the screening of all animals is mandatory to discard those with previous natural immunity. The most common technique used in the screening is the plaque reduction neutralization test (PRNT). However, most recent studies points to the cell-mediated immunity (CMI) as an important player in the process of controlling Dengue virus (DENV) infections. Here we presented the results from the screening of 55 rhesus monkeys housed in an animal breeding facility at Quang Ninh province, Vietnam. We evaluated the neutralizing antibody response by PRNT and determined the levels of interferon γ (IFNγ)-secretion after the viral stimulation of monkey-peripheral blood mononuclear cells, by enzyme-linked immunosorbent assay (ELISA). We found no correspondence between PRNT and IFNγ-ELISA. In fact, 19 animals were positive only by IFNγ-ELISA. Moreover, to study the protective capacity of the CMI detected, three animals with positive response by IFNγ-ELISA and negative by PRNT were inoculated with an infective preparation of DENV-3 and, as a result, no viremia was detected during 10 days after the challenge. This fact points to the importance of screening non-human primates through a CMI assay together with PRNT. This procedure should discard those false-negative cases which would be protected after the viral challenge in the immunization schedule.

Identifiers

PMID28435678
PMCPMC5382433
OpenAlexW2597703794

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.