Evidence map›Paper›PMID 24711617›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

CD8+ T cells define an unexpected role in live-attenuated vaccine protective immunity against Chlamydia trachomatis infection in macaques.

Norma Olivares-Zavaleta, William M Whitmire, Laszlo Kari, Gail L Sturdevant, Harlan D Caldwell

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. CD8iScience · 2026
    Article
  4. AFrontiers in immunology · 2026
    Article
  5. Article
  6. Article
  7. Frontiers in cellular and infection microbiology · 2025
    Article
  8. Intranasal delivery ofHuman vaccines & immunotherapeutics · 2024
    Article
  9. Viral Vector-BasedVaccines · 2024
    Article
  10. Article
  11. Article
  12. Diverse animal models forFrontiers in microbiology · 2024
    Review
  13. Article
  14. Multi-component prime-boostFrontiers in immunology · 2022
    Article
  15. Article
  16. Article
  17. Seventy Years ofFrontiers in microbiology · 2019
    Review
  18. Article
  19. Considerations for the rational design of a Chlamydia vaccine.Human vaccines & immunotherapeutics · 2017
    Review
  20. The Predominant CD4Clinical and vaccine immunology : CVI · 2017
    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 at 2 institutions in 1 country.

Norma Olivares-ZavaletaLaboratory of Intracellular Parasites, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840.
William M Whitmire
Laszlo Kari
Gail L Sturdevant
Harlan D Caldwell
National Institutes of Health · USNational Institute of Allergy and Infectious Diseases · US

Funding

Pathogensis of Chlamydial InfectionZIAAI000845 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CALDWELL, HARLAN D · 2009 to 2022
$14.8M
Chlamydial Immunity and Vaccine DevelopmentZIAAI000672 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CALDWELL, HARLAN D · 2009 to 2016
$6.8M
Intramural NIH HHS ZIA AI000672
6 · The paper itself

Abstract

Trachoma, caused by the obligate intracellular organism Chlamydia trachomatis, is the world's leading cause of preventable blindness for which a vaccine is needed. We have previously shown that a plasmid-deficient live-attenuated trachoma vaccine delivered ocularly to macaques elicited either solid or partial protective immunity against a virulent ocular challenge. Solidly protected macaques shared the same MHC class II alleles implicating CD4(+) T cells in superior protective immunity. Understandably, we sought to define T cell immune correlates in these animals to potentially improve vaccine efficacy. In this study, following a 2-y resting period, these macaques were boosted i.m. with the live-attenuated trachoma vaccine and their peripheral T cell anamnestic responses studied. Both solidly and partially protected macaques exhibited a CD4(+) and CD8(+) T cell anamnestic response following booster immunization. CD8(+) but not CD4(+) T cells from solidly protected macaques proliferated against soluble chlamydial Ag. We observed a more rapid T cell inflammatory cytokine response in tears of solidly protected animals following ocular rechallenge. Most notably, depletion of CD8(+) T cells in solidly protected macaques completely abrogated protective immunity. Collectively, our findings support the conclusion that CD8(+) T cells play an important but unexpected role in live-attenuated trachoma vaccine-mediated protective immunity.

Indexed as

AnimalsBacterial VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationChlamydia trachomatisFemaleMacaca nemestrinaMaleTrachomaVaccines, AttenuatedBacterial VaccinesVaccines, Attenuated

Identifiers

PMID24711617
PMCPMC4023123
OpenAlexW2149535469

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.