Evidence map›Paper›PMID 12457287›Full record

ArticleGene therapy2002

Encapsulation of recombinant adenovirus into alginate microspheres circumvents vector-specific immune response.

G Sailaja, H HogenEsch, A North, J Hays, S K Mittal

Open access · greenAbstract read
In one paragraph

Article in Gene therapy, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-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

44 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
  2. Developing the next-generation of adenoviral vector vaccines.Human vaccines & immunotherapeutics · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Manganese Mineralization of Pathogenic Viruses as a Universal Vaccine Platform.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  8. Review
  9. Review
  10. Article
  11. COVID-19 Vaccines: An Overview of Different Platforms.Bioengineering (Basel, Switzerland) · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. MicroRNA delivery for regenerative medicine.Advanced drug delivery reviews · 2015
    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

5 authors at 2 institutions in 1 country.

G SailajaDepartment of Veterinary Pathobiology, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA.
H HogenEsch
A North
J Hays
S K Mittal
Purdue University West Lafayette · USUnited States Military Academy · US

Funding

NONHUMAN ADENOVIRUS VECTORS FOR GENE THERAPYR29GM055168 · NIGMS · PURDUE UNIVERSITY WEST LAFAYETTE · PI MITTAL, SURESH K · 1997 to 2001
$220k
NIGMS NIH HHS GM5516
6 · The paper itself

Abstract

Pre-existing immunity against adenoviruses may compromise the efficacy of adenoviral vectors for vaccination and gene therapy. The purpose of this study was to determine whether encapsulation of adenovirus recombinants into biodegradable alginate microparticles could circumvent the vector-specific immune response. Mice were immunized either intranasally (i.n.) or intraperitoneally (i.p.) with human adenovirus type 5 (HAd5), resulting in the development of virus-specific antibodies. Immunized and nai;ve mice were inoculated with AdCA36lacZ (an E1-deleted HAd5 recombinant containing the bacterial beta-galactosidase (LacZ) gene), encapsulated (E) into alginate microparticles, or nonencapsulated (NE) ie, as a virus suspension. LacZ expression in animals immunized once (1x) or twice (2x) with HAd5 and subsequently inoculated with NE-AdCA36lacZ (NE-Z) was significantly (P<0.001) reduced compared to those levels observed in NE-Z inoculated nai;ve mice, suggesting that the immune response against the vector adversely affected transgene expression. In contrast, there was only slight reduction (P>0.05) in LacZ expression in mice immunized 1x or 2x with HAd5 that were subsequently inoculated with E-AdCA36lacZ (E-Z) compared to those levels obtained in E-Z inoculated nai;ve animals. Similar results were obtained with i.n. or i.p. inoculated animals. These results indicate that microencapsulation of recombinant adenovirus effectively circumvented the vector-specific immune response.

Indexed as

AlginatesBiocompatible MaterialsGenetic VectorsAdenoviridaeAdministration, IntranasalAnimalsAntibodies, ViralEnzyme-Linked Immunosorbent AssayFemaleGene ExpressionGenetic EngineeringGlucuronic AcidHexuronic AcidsImmunoglobulin AImmunoglobulin GInjections, IntraperitonealAlginatesAntibodies, ViralBiocompatible MaterialsGlucuronic AcidHexuronic AcidsImmunoglobulin AImmunoglobulin G

Identifiers

PMID12457287
PMCPMC1459421
OpenAlexW2000464877

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.