Evidence map›Paper›PMID 10074183›Full record

ArticleJournal of virology1999

Comparison of immunity generated by nucleic acid-, MF59-, and ISCOM-formulated human immunodeficiency virus type 1 vaccines in Rhesus macaques: evidence for viral clearance.

E J Verschoor, P Mooij, H Oostermeijer, M van der Kolk, P ten Haaft, B Verstrepen, Y Sun, B Morein, L Akerblom, D H Fuller and 2 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Modulation of HIV-1 immunity by adjuvants.Current opinion in HIV and AIDS · 2014
    Review
  3. Article
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  6. Review
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  13. Article
  14. Viral nanoparticles and virus-like particles: platforms for contemporary vaccine design.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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 at 3 institutions in 3 countries.

E J VerschoorDepartment of Virology, Biomedical Primate Research Center, Rijswijk, The Netherlands.
P Mooij
H Oostermeijer
M van der Kolk
P ten Haaft
B Verstrepen
Y Sun
B Morein
L Akerblom
D H Fuller
S W Barnett
J L Heeney
Biomedical Primate Research Centre · NLChiron (Norway) · NOGlobal Vaccines (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kinetics of T-helper immune responses generated in 16 mature outbred rhesus monkeys (Macaca mulatta) within a 10-month period by three different human immunodeficiency virus type 1 (HIV-1) vaccine strategies were compared. Immune responses to monomeric recombinant gp120SF2 (rgp120) when the protein was expressed in vivo by DNA immunization or when it was delivered as a subunit protein vaccine formulated either with the MF59 adjuvant or by incorporation into immune-stimulating complexes (ISCOMs) were compared. Virus-neutralizing antibodies (NA) against HIV-1SF2 reached similar titers in the two rgp120SF2 protein-immunized groups, but the responses showed different kinetics, while NA were delayed and their levels were low in the DNA-immunized animals. Antigen-specific gamma interferon (IFN-gamma) T-helper (type 1-like) responses were detected in the DNA-immunized group, but only after the fourth immunization, and the rgp120/MF59 group generated both IFN-gamma and interleukin-4 (IL-4) (type 2-like) responses that appeared after the third immunization. In contrast, rgp120/ISCOM-immunized animals rapidly developed marked IL-2, IFN-gamma (type 1-like), and IL-4 responses that peaked after the second immunization. To determine which type of immune responses correlated with protection from infection, all animals were challenged intravenously with 50 50% infective doses of a rhesus cell-propagated, in vivo-titrated stock of a chimeric simian immunodeficiency virus-HIVSF13 construct. Protection was observed in the two groups receiving the rgp120 subunit vaccines. Half of the animals in the ISCOM group were completely protected from infection. In other subunit vaccinees there was evidence by multiple assays that virus detected at 2 weeks postchallenge was effectively cleared. Early induction of potent type 1- as well as type 2-like T-helper responses induced the most-effective immunity.

Indexed as

Immunity, CellularAcquired Immunodeficiency SyndromeAdjuvants, ImmunologicAIDS VaccinesAnimalsChemistry, PharmaceuticalHIV-1HIV Envelope Protein gp120HumansISCOMsMacaca mulattaPolysorbatesRecombinant ProteinsSqualeneAdjuvants, ImmunologicAIDS VaccinesHIV Envelope Protein gp120ISCOMsMF59 oil emulsionPolysorbatesRecombinant ProteinsSqualene

Identifiers

PMID10074183
PMCPMC104093
OpenAlexW2106014927

What OpenQuestion holds

Texttitle and abstract
measurements read1
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.