Evidence map›Paper›PMID 11507213›Full record

Trial reportJournal of virology2001

Polymorphisms in HLA class I genes associated with both favorable prognosis of human immunodeficiency virus (HIV) type 1 infection and positive cytotoxic T-lymphocyte responses to ALVAC-HIV recombinant canarypox vaccines.

R A Kaslow, C Rivers, J Tang, T J Bender, P A Goepfert, R El Habib, K Weinhold, M J Mulligan, NIAID AIDS vaccine evaluation group

Open access · greenAbstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in Journal of virology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.2field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 101 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 4 institutions in 3 countries.

R A KaslowDepartment of Epidemiology and International Health, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA. rkaslow@uab.edu
C Rivers
J Tang
T J Bender
P A Goepfert
R El Habib
K Weinhold
M J Mulligan
NIAID AIDS vaccine evaluation group
University of Alabama at Birmingham · USNational School of Public Health · GRDuke University · USFaculty of Public Health · GB

Funding

GENETIC FACTORS IN THE EPIDEMIOLOGY OF HIV1 INFECTIONR01AI041951 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KASLOW, RICHARD ALAN · 1997 to 2005
$1.8M
AIDS VACCINE EVALUATION UNITSN01AI045209 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MULLIGAN, MARK JOSEPH · 1994 to 2000
$379k
NIAID NIH HHS AI 41951NIAID NIH HHS AI 45209NIAID NIH HHS R01 AI041951
6 · The paper itself

Abstract

Carriers of certain human leukocyte antigen class I alleles show favorable prognosis of human immunodeficiency virus type 1 (HIV-1) infection, presumably due to effective CD8(+) cytotoxic T-lymphocyte responses, but close relationships between class I variants mediating such responses to natural and to vaccine HIV-1 antigen have not been established. During 6 to 30 months of administration and follow-up in trials of ALVAC-HIV recombinant canarypox vaccines, cells from 42% of 291 HIV-1-negative vaccinated subjects typed at class I loci responded to an HIV-1 protein in a lytic bulk CD8(+) cytotoxic T-lymphocyte assay. By 2 weeks after the second dose, higher proportions of vaccinees carrying one of two alleles consistently associated with slower progression of natural HIV-1 infection reacted at least once: B*27 carriers reacted to Gag (64%; odds ratio [OR] = 10.3, P = 0.001) and Env (36%; OR = 4.6, P = 0.04), and B*57 carriers reacted to Env (44%; OR = 6.6, P < 0.05). By 2 weeks after the third or fourth dose, B*27 carriers had responded (two or more reactions) to Gag (33%; OR = 4.4, P < 0.05) and B*57 carriers had responded to both Gag (39%; OR = 5.3, P = 0.013) and Env (39%; OR = 9.5, P = 0.002). Homozygosity at class I loci, although conferring an unfavorable prognosis following natural infection, showed no such disadvantage for vaccine response. Individual class I alleles have not previously demonstrated such clear and consistent relationship with both the clinical course of an infection and cellular immunity to a vaccine against the infectious agent. This proof of principle that class I an alleles modulate both processes has implications for development of HIV-1 and presumably other vaccines.

Indexed as

Genes, MHC Class IPolymorphism, GeneticAdolescentAdultAIDS VaccinesAllelesAvipoxvirusDouble-Blind MethodGenetic VectorsHaplotypesHIV-1HIV InfectionsHLA-A AntigensHLA-B AntigensHLA-C AntigensHomozygoteAIDS VaccinesHLA-A AntigensHLA-B AntigensHLA-C AntigensVaccines, Synthetic

Identifiers

PMID11507213
PMCPMC115113
OpenAlexW2170327206

What OpenQuestion holds

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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.