Evidence map›Paper›PMID 20357087›Full record

ArticleJournal of virology2010

Route of adenovirus-based HIV-1 vaccine delivery impacts the phenotype and trafficking of vaccine-elicited CD8+ T lymphocytes.

David R Kaufman, Maytal Bivas-Benita, Nathaniel L Simmons, Darby Miller, Dan H Barouch

Abstract readEvaluation Study
In one paragraph

Article in Journal of virology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
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

42 citing papers in PubMed.

  1. Article
  2. Adenovirus vector-based vaccine for infectious diseases.Drug metabolism and pharmacokinetics · 2022
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. New prospects for a preventive HIV-1 vaccine.Journal of virus eradication · 2015
    Article
  17. Progress on adenovirus-vectored universal influenza vaccines.Human vaccines & immunotherapeutics · 2015
    Review
  18. Article
  19. Article
  20. Article
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.

David R KaufmanDivision of Vaccine Research, Beth Israel Deaconess Medical Center, E/CLS 1047, 330 Brookline Avenue, Boston, MA 02215, USA.
Maytal Bivas-Benita
Nathaniel L Simmons
Darby Miller
Dan H Barouch

Funding

The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ROBERT A. PARKER · 2004 to 2026
$94.4M
Preclinical Evaluation of Novel Adenovirus Prime-Boost HIV-1 VaccineU19AI078526 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BAROUCH, DAN H. · 2008 to 2012
$44.0M
Preclinical Evaluation of Novel Adenovirus VectorsU19AI066305 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GOUDSMIT, JAAP · 2005 to 2009
$19.8M
Novel Adenovirus Vaccine Vectors for HIV/SIVR01AI066924 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BAROUCH, DAN H. · 2006 to 2010
$3.5M
Induction of Mucosal Cellular Immunity by HIV-1 Vaccine VectorsK08AI083079 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KAUFMAN, DAVID ROSS · 2009 to 2010
$253k
NIAID NIH HHS K08 AI083079NIAID NIH HHS P30 AI060354NIAID NIH HHS R01 AI066924NIAID NIH HHS U19 AI066305NIAID NIH HHS U19 AI078526
6 · The paper itself

Abstract

Candidate HIV-1 vaccine regimens utilizing intramuscularly (i.m.) administered recombinant adenovirus (rAd)-based vectors can induce potent mucosal cellular immunity. However, the degree to which mucosal rAd vaccine routing might alter the quality and anatomic distribution of vaccine-elicited CD8(+) T lymphocytes remains unclear. We show that the route of vaccination critically impacts not only the magnitude but also the phenotype and trafficking of antigen-specific CD8(+) T lymphocytes in mice. I.m. rAd immunization induced robust local transgene expression and elicited high-frequency, polyfunctional CD8(+) T lymphocytes that trafficked broadly to both systemic and mucosal compartments. In contrast, intranasal (i.n.) rAd immunization led to similarly robust local transgene expression but generated low-frequency, monofunctional CD8(+) T lymphocytes with restricted anatomic trafficking patterns. Respiratory rAd immunization elicited systemic and mucosal CD8(+) T lymphocytes with phenotypes and trafficking properties distinct from those elicited by i.m. or i.n. rAd immunization. Our findings indicate that the anatomic microenvironment of antigen expression critically impacts the phenotype and trafficking of antigen-specific CD8(+) T lymphocytes.

Indexed as

AdenoviridaeAdministration, IntranasalAIDS VaccinesAnimalsAntibodies, ViralCD8-Positive T-LymphocytesCells, CulturedDisease Models, AnimalDrug Delivery SystemsGenetic VectorsHIV InfectionsHumansInjections, IntramuscularMiceMice, Inbred BALB CMice, Inbred C57BLAIDS VaccinesAntibodies, Viral

Identifiers

PMID20357087
PMCPMC2876628

What OpenQuestion holds

Textmetadata
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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.