Evidence map›Paper›PMID 12228286›Full record

ArticleInfection and immunity2002

Enhanced immunogenicity of pneumococcal surface adhesin A by genetic fusion to cytokines and evaluation of protective immunity in mice.

Dennis O Gor, Xuedong Ding, Qing Li, John R Schreiber, Michael Dubinsky, Neil S Greenspan

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 31 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

6 authors at 2 institutions in 2 countries.

Dennis O GorInstitute of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4943, USA.
Xuedong Ding
Qing Li
John R Schreiber
Michael Dubinsky
Neil S Greenspan
Taipei Institute of Pathology · TWUniversity School · US

Funding

IGG SUBCLASS &FUNCTION OF ANTIPOLYSACCHARIDE ANTIBODYR01AI032596 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SCHREIBER, JOHN R · 1993 to 2005
$1.9M
HUMAN T CELL RESPONSE TO PNEUMOCOCCAL CONJUGATE VACCINESR01AI046667 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SCHREIBER, JOHN R · 2000 to 2004
$1.5M
TRAINING GRANT IN IMMUNOLOGYT32AI007427 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI LAMM, MICHAEL E. · 1995 to 2004
$877k
IMMUNOGENICITY OF PNEUMOCOCCAL CONJUGATE VACCINESR01AI041657 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI GREENSPAN, NEIL S · 1997 to 2001
$476k
NIAID NIH HHS R01 AI032596NIAID NIH HHS R01 AI046667NIAID NIH HHS R01-AI32596NIAID NIH HHS R01-AI41657NIAID NIH HHS R01-AI46667NIAID NIH HHS T32 AI007427NIAID NIH HHS T32-AI07427
6 · The paper itself

Abstract

Immunization of mice with pneumococcal surface adhesin A (PsaA) emulsified in complete Freund's adjuvant (CFA) provides protection against systemic infection with Streptococcus pneumoniae. Because the use of CFA is not acceptable in humans, we sought to develop alternative means of enhancing the immunogenicity of protein antigens of potential use in pneumococcal vaccines. We designed a series of genetic constructs in which coding sequences for PsaA were linked to sequences encoding either murine interleukin-2 (mIL-2), mIL-4, or two copies of an immunostimulatory nonapeptide derived from mIL-1beta. The PsaA-cytokine constructs were cloned and expressed in Escherichia coli. Mice immunized twice with PsaA-IL-2, or PsaA-IL-4 responded with PsaA-specific antibody production comparable in magnitude to that of mice primed with PsaA in CFA and boosted with PsaA in incomplete Freund's adjuvant (PsaA-Adj). Antibodies elicited by PsaA-Adj were predominantly of the immunoglobulin G1 (IgG1) subclass, while PsaA-IL-2 and PsaA-IL-4 elicited substantial amounts of IgG2a in addition to IgG1. Mice immunized with PsaA-Adj or PsaA-IL-4 were partially protected against intraperitoneal challenge with virulent S. pneumoniae (30% overall survival beyond 15 days postchallenge). Mice immunized with PsaA and no adjuvant or PsaA-IL-2 exhibited 0 or 5% survival rates, respectively, following challenge. In contrast, mice immunized twice with capsular polysaccharide were 100% protected. The modest levels of protection seen in mice immunized with PsaA and its more immunogenic derivatives may be explained in part by the relative inaccessibility of antibody to PsaA on the surface of encapsulated S. pneumoniae.

Indexed as

Membrane Transport ProteinsAdhesins, BacterialAnimalsAntibodies, BacterialArtificial Gene FusionBacterial AdhesionBacterial ProteinsBase SequenceCarrier ProteinsCytokinesDNA, RecombinantFluorescent Antibody Technique, IndirectInterleukin-2Interleukin-4LipoproteinsMiceAdhesins, BacterialAntibodies, BacterialBacterial ProteinsCarrier ProteinsCytokinesDNA, RecombinantInterleukin-2Interleukin-4LipoproteinsMembrane Transport ProteinsPneumococcal VaccinesPsaA protein, StreptococcusRecombinant Fusion ProteinsVaccines, Synthetic

Identifiers

PMID12228286
PMCPMC128336
OpenAlexW2105204683

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.