Evidence map›Paper›PMID 25891359›Full record

ArticleHuman vaccines & immunotherapeutics2015

Experimental studies of a vaccine formulation of recombinant human VEGF antigen with aluminum phosphate.

Lincidio Pérez Sánchez, Yanelys Morera Díaz, Mónica Bequet-Romero, Gerardo Ramses Hernández, Yadira Rodríguez, Jorge Castro Velazco, Pedro Puente Pérez, Marta Ayala Avila, Jorge V Gavilondo

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Lincidio Pérez Sáncheza Cancer Immunotherapy Laboratory; Department of Pharmaceuticals; Center for Genetic Engineering and Biotechnology (CIGB) ; Playa Cubanacan , Havana , Cuba.
Yanelys Morera Díaz
Mónica Bequet-Romero
Gerardo Ramses Hernández
Yadira Rodríguez
Jorge Castro Velazco
Pedro Puente Pérez
Marta Ayala Avila
Jorge V Gavilondo
Centro de Ingeniería Genética y Biotecnología · CUCuban Neuroscience Center · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CIGB-247 is a cancer vaccine that is a formulation of a recombinant protein antigen representative of the human vascular endothelial growth factor (VEGF) with a bacterially-derived adjuvant (VSSP). The vaccine has shown an excellent safety profile in mice, rats, rabbits, not-human primates and in recent clinical trials in cancer patients. Response to the vaccine is characterized by specific antibody titers that neutralize VEGF/VEGFR2 binding and a cytotoxic tumor-specific response. To expand our present anti-VEGF active immunotherapy strategies, we have now studied in mice and non-human primates the effects of vaccination with a formulation of our recombinant VEGF antigen and aluminum phosphate adjuvant (hereafter denominated CIGB-247-A). Administered bi-weekly, CIGB-247-A produces high titers of anti-VEGF IgG blocking antibodies in 2 mice strains. Particularly in BALB/c, the treatment impaired subcutaneous F3II mammary tumor growth and reduced the number of spontaneous lung macro metastases, increasing animals' survival. Spleen cells from specifically immunized mice directly killed F3II tumor cells in vitro. CIGB-247-A also showed to be immunogenic in non-human primates, which developed anti-VEGF blocking antibodies and the ability for specific direct cell cytotoxic responses, all without impairing the healing of deep skin wounds or other side effect. Our results support consideration of aluminum phosphate as a suitable adjuvant for the development of new vaccine formulations using VEGF as antigen.

Indexed as

Chemistry, PharmaceuticalAdjuvants, ImmunologicAluminum CompoundsAnimalsAntibodies, NeutralizingCancer VaccinesChlorocebus aethiopsCytotoxicity, ImmunologicFemaleImmunization ScheduleLeukocytes, MononuclearMaleMammary Neoplasms, AnimalMammary Neoplasms, ExperimentalMice, Inbred BALB CMice, Inbred C57BLAdjuvants, ImmunologicAluminum Compoundsaluminum phosphateAntibodies, NeutralizingCancer VaccinesPhosphatesVaccines, SyntheticVascular Endothelial Growth Factor AadjuvantAluminum phosphateANOVA, Analysis of Varianceantibodiescancer therapeutic vaccineCFSE, Carboxyfluorescein succinimidyl esterCTL, Cytotoxic T lymphocyteELISA, Enzyme-linked immune-sorbent assayFACS, Fluorescence-activated cell sortingGST, Glutathione S-transferaseHPLC, High-performance liquid chromatographyKDR, kinase domain receptorNi-NTA, nickel-nitrilotriacetic acidPBMC, Peripheral blood mononuclear cellsVEGFVEGFR2, vascular endothelial growth factor receptor 2VEGF, vascular endothelial growth factorVSSP, very small sized proteoliposomes

Identifiers

PMID25891359
PMCPMC4635891
OpenAlexW1599445372

What OpenQuestion holds

Textmetadata
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.