Evidence map›Paper›PMID 18285494›Full record

ArticleInfection and immunity2008

Enhancement of antibody responses to Bacillus anthracis protective antigen domain IV by use of calreticulin as a chimeric molecular adjuvant.

Yong Sung Park, Jin Hyup Lee, Chien-Fu Hung, T-C Wu, Tae Woo Kim

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Calreticulin as an AdjuvantJournal of immunology research · 2022
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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

5 authors at 2 institutions in 4 countries.

Yong Sung ParkLaboratory of Infection and Immunology, Graduate School of Medicine, Korea University, Seoul, South Korea.
Jin Hyup Lee
Chien-Fu Hung
T-C Wu
Tae Woo Kim
Korea University · KRBeijing Obstetrics and Gynecology Hospital · CN

Funding

Dev. of Optimized/Adjuvanted Smallpox DNA Vaccine (Gene Gun)U01AI070346 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WU, TZYY-CHOOU · 2006 to 2009
$1.4M
NIAID NIH HHS 1 U01 AI070346-01NIAID NIH HHS U01 AI070346
6 · The paper itself

Abstract

The generation of protective humoral immune responses against the receptor-binding domain (domain IV) of protective antigen [PA(dIV)] of Bacillus anthracis represents a plausible approach against anthrax toxin. In the current study, we have developed a naked DNA vaccine encoding calreticulin (CRT) linked to PA(dIV) of Bacillus anthracis [CRT/PA(dIV)]. We transfected a human embryonic kidney cell line (HEK 293) with CRT/PA(dIV) DNA and performed Western blotting and confocal microscopy analysis. We found that linkage of CRT to PA(dIV) targets PA(dIV) to the endoplasmic reticulum, resulting in secretion of the chimeric CRT/PA(dIV) protein. We then evaluated the ability of CRT/PA(dIV) DNA to generate PA(dIV)-specific antibody responses and protective immunity against lethal anthrax toxin (PA plus lethal factor) challenge. We found that mice immunized with CRT/PA(dIV) DNA were capable of rapidly inducing significantly higher PA(dIV)-specific antibody responses than mice immunized with PA(dIV) DNA alone. Furthermore, we observed that this enhanced antibody response generated by CRT/PA(dIV) DNA was CD4 dependent, since CD4 knockout mice demonstrated a significant reduction in antibody responses. In addition, analysis of the titers and avidity maturation of the induced PA-specific antibodies revealed that vaccination with CRT/PA(dIV) DNA vaccine accelerated the avidity maturation of antibodies to PA(dIV) compared to vaccination with PA(dIV) DNA. Importantly, the enhanced antibody responses correlated to protective immunity against lethal anthrax toxin challenge. Thus, DNA vaccines encoding CRT linked to PA(dIV) may dramatically enhance PA-specific protective antibody responses. Our results have significant clinical applications for biodefense against anthrax toxin.

Indexed as

Adjuvants, ImmunologicAnimalsAnthraxAnthrax VaccinesAntibodies, BacterialAntibody AffinityAntigens, BacterialBacillus anthracisBacterial ToxinsCalreticulinCD4 AntigensCell LineEndoplasmic ReticulumFemaleHumansImmunoglobulin GAdjuvants, Immunologicanthrax toxinAnthrax VaccinesAntibodies, BacterialAntigens, BacterialBacterial ToxinsCalreticulinCD4 AntigensImmunoglobulin GImmunoglobulin MRecombinant Fusion ProteinsVaccines, DNA

Identifiers

PMID18285494
PMCPMC2346671
OpenAlexW2160960669

What OpenQuestion holds

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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.