Evidence map›Paper›PMID 11932387›Full record

ArticleJournal of virology2002

Effect of the V3 loop deletion of envelope glycoprotein on cellular responses and protection against challenge with recombinant vaccinia virus expressing gp160 of primary human immunodeficiency virus type 1 isolates.

Irena Kiszka, Dariusz Kmieciak, Jaroslaw Gzyl, Toshio Naito, Elizabeth Bolesta, Aleksander Sieron, Satya P Singh, Alagarsamy Srinivasan, Giorgio Trinchieri, Yutaro Kaneko and 1 more

Abstract read
In one paragraph

Article in Journal of virology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

9 citing papers in PubMed, 17 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

11 authors at 5 institutions in 2 countries.

Irena KiszkaCenter for Neurovirology and Cancer Biology, Temple University, Philadelphia, Pennsylvania 19122, USA.
Dariusz Kmieciak
Jaroslaw Gzyl
Toshio Naito
Elizabeth Bolesta
Aleksander Sieron
Satya P Singh
Alagarsamy Srinivasan
Giorgio Trinchieri
Yutaro Kaneko
Danuta Kozbor
Temple University · USThomas Jefferson University · USAjinomoto (Japan) · JPHahnemann University Hospital · USThe Wistar Institute · US

Funding

THE ILLINOIS FAMILIES STUDY: CHILD WELL-BEINGR01HD039148 · NICHD · NORTHWESTERN UNIVERSITY · PI HOLL, JANE LOUISE · 2000 to 2004
$2.3M
IMMUNOBIOLOGY OF INTERLUKIN-12R01AI034412 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J. · 1994 to 2003
$1.4M
NIAID NIH HHS AI34412NIAID NIH HHS AI/HD39148NIAID NIH HHS R01 AI034412NICHD NIH HHS R01 HD039148
6 · The paper itself

Abstract

The magnitude and breadth of cytotoxic-T-lymphocyte (CTL) responses induced by human immunodeficiency virus type 1 (HIV-1) envelope protein from which the hypervariable V3 loop had been deleted (DeltaV3) were evaluated in the HLA-A2/K(b) transgenic mice. It was demonstrated that vaccines expressing the DeltaV3 mutant of either HIV-1(IIIB) or HIV-1(89.6) envelope glycoprotein induced broader CD8(+) T-cell activities than those elicited by the wild-type (WT) counterparts. Specifically, the differences were associated with higher responses to conserved HLA-A2-restricted CTL epitopes of the envelope glycoprotein and could be correlated with an increased cell surface occupancy by the epitope-HLA-A2 complexes in target cells expressing the DeltaV3 mutant. Using recombinant vaccinia virus expressing heterologous gp160 of primary HIV-1 isolates in a murine challenge system, we observed that the extent of resistance to viral transmission was higher in animals immunized with the DeltaV3 than the WT envelope vaccine. The protection was linked to the presence of envelope-specific CD8(+) T cells, since depletion of these cells by anti-CD8 antibody treatment at the time of challenge abolished the vaccine-induced protection. The results from our studies provide insights into approaches for boosting the breadth of envelope-specific CTL responses.

Indexed as

Gene DeletionAIDS VaccinesAnimalsCytotoxicity Tests, ImmunologicH-2 AntigensHIV-1HIV Envelope Protein gp120HIV Envelope Protein gp160HIV InfectionsHLA-A2 AntigenHumansMiceMice, Inbred C57BLMice, Inbred DBAMice, TransgenicPeptide FragmentsAIDS VaccinesH-2 AntigensH-2Kb protein, mouseHIV Envelope Protein gp120HIV envelope protein gp120 (305-321)HIV Envelope Protein gp160HLA-A2 AntigenPeptide Fragments

Identifiers

PMID11932387
PMCPMC155109
OpenAlexW2125384971

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.