Evidence map›Paper›PMID 20188250›Full record

ArticleVaccine2010

Systemic immunization with CCL27/CTACK modulates immune responses at mucosal sites in mice and macaques.

Kimberly A Kraynyak, Michele A Kutzler, Neil J Cisper, Amir S Khan, Ruxandra Draghia-Akli, Niranjan Y Sardesal, Mark G Lewis, Jian Yan, David B Weiner

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. DNA-based immunotherapy for cancer: In vivo approaches for recalcitrant targets.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Critical roles of chemokine receptor CCR10 in regulating memory IgA responses in intestines.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  20. 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

9 authors at 4 institutions in 1 country.

Kimberly A KraynyakDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6100, United States.
Michele A Kutzler
Neil J Cisper
Amir S Khan
Ruxandra Draghia-Akli
Niranjan Y Sardesal
Mark G Lewis
Jian Yan
David B Weiner
University of Pennsylvania · USInovio Pharmaceuticals (United States) · USBioqual · USDrexel University · US

Funding

Active Immune Therapy and HAART for HIV-1 InfectionU19AI048241 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WEINER, DAVID B. · 2004 to 2009
$2.2M
TNT: Targeting and Triggering Adjuvancy of DNA VaccinesF32AI054152 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI KUTZLER, MICHELE AILEEN · 2003 to 2005
$139k
NIAID NIH HHS F32 AI054152NIAID NIH HHS F32AI054152NIAID NIH HHS U19 AI048241PHS HHS 1-T32-A107632
6 · The paper itself

Abstract

Plasmid DNA is a promising vaccine platform that has been shown to be safe and able to be administered repeatedly without vector interference. Enhancing the potency of DNA vaccination through co-delivery of molecular adjuvants is one strategy currently under investigation. Here we describe the use of the novel chemokine adjuvant CCL27/CTACK to enhance immune responses to an HIV-1 or SIV antigen in mice and rhesus macaques. CCL27 has been shown to play a role in inflammatory responses through chemotaxis of CCR10+ cells, and we hypothesized that CCL27 may modulate adaptive immune responses. Immunizations in mice with HIV-1gag/CCL27 enhanced immune responses both at peripheral and, surprisingly, at mucosal sites. To confirm these findings in a large-animal model, we created optimized CCL27 and SIV antigenic plasmid constructs for rhesus macaques. 10 macaques (n=5/group) were immunized intramuscularly with 1mg/construct of antigenic plasmids+/-CCL27 with electroporation. We observed significant IFN-gamma secretion and CD8+ T-cell proliferation in peripheral blood. Interestingly, CCL27 co-immunized macaques exhibited a trend toward greater effector CD4+ T cells in the bronchiolar lavage (BAL). CCL27 co-delivery also elicited greater antigen-specific IgA at unique sites including BAL and fecal samples but not in the periphery. Future studies incorporating CCL27 as an adjuvant in vaccine or therapy models where eliciting immune responses in the lung are warranted.

Indexed as

Adjuvants, ImmunologicAIDS VaccinesAnimalsAntibodies, ViralBronchoalveolar Lavage FluidCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationChemokine CCL27Femalegag Gene Products, Human Immunodeficiency VirusImmunizationImmunoglobulin AInterferon-gammaMacacaMiceAdjuvants, ImmunologicAIDS VaccinesAntibodies, ViralChemokine CCL27gag Gene Products, Human Immunodeficiency VirusImmunoglobulin AInterferon-gammaSAIDS VaccinesVaccines, DNA

Identifiers

PMID20188250
PMCPMC4396814
OpenAlexW2030064520

What OpenQuestion holds

Textmetadata
LicenceTDM
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.