Evidence map›Paper›PMID 21628568›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Approach to discover T- and B-cell antigens of intracellular pathogens applied to the design of Chlamydia trachomatis vaccines.

Oretta Finco, Elisabetta Frigimelica, Francesca Buricchi, Roberto Petracca, Giuliano Galli, Elisa Faenzi, Eva Meoni, Alessandra Bonci, Mauro Agnusdei, Filomena Nardelli and 12 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 88 citations in OpenAlex.

  1. Trial
  2. CD8iScience · 2026
    Article
  3. Article
  4. Advances inMicroorganisms · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Considerations for the rational design of a Chlamydia vaccine.Human vaccines & immunotherapeutics · 2017
    Review
  14. Update on Chlamydia trachomatis Vaccinology.Clinical and vaccine immunology : CVI · 2017
    Review
  15. Article
  16. Review
  17. Antibody to Chlamydia trachomatis proteins, TroA and HtrA, as a biomarker for Chlamydia trachomatis infection.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2017
    Article
  18. Article
  19. Review
  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

22 authors at 2 institutions in 1 country.

Oretta FincoNovartis Vaccines and Diagnostics, 53100 Siena, Italy.
Elisabetta Frigimelica
Francesca Buricchi
Roberto Petracca
Giuliano Galli
Elisa Faenzi
Eva Meoni
Alessandra Bonci
Mauro Agnusdei
Filomena Nardelli
Erika Bartolini
Maria Scarselli
Elena Caproni
Donatello Laera
Luisanna Zedda
David Skibinski
Serena Giovinazzi
Riccardo Bastone
Elvira Ianni
Roberto Cevenini
Guido Grandi
Renata Grifantini
Novartis (Italy) · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural immunity against obligate and/or facultative intracellular pathogens is usually mediated by both humoral and cellular immunity. The identification of those antigens stimulating both arms of the immune system is instrumental for vaccine discovery. Although high-throughput technologies have been applied for the discovery of antibody-inducing antigens, few examples of their application for T-cell antigens have been reported. We describe how the compilation of the immunome, here defined as the pool of immunogenic antigens inducing T- and B-cell responses in vivo, can lead to vaccine candidates against Chlamydia trachomatis. We selected 120 C. trachomatis proteins and assessed their immunogenicity using two parallel high-throughput approaches. Protein arrays were generated and screened with sera from C. trachomatis-infected patients to identify antibody-inducing antigens. Splenocytes from C. trachomatis-infected mice were stimulated with 79 proteins, and the frequency of antigen-specific CD4(+)/IFN-γ(+) T cells was analyzed by flow cytometry. We identified 21 antibody-inducing antigens, 16 CD4(+)/IFN-γ(+)-inducing antigens, and five antigens eliciting both types of responses. Assessment of their protective activity in a mouse model of Chlamydia muridarum lung infection led to the identification of seven antigens conferring partial protection when administered with LTK63/CpG adjuvant. Protection was largely the result of cellular immunity as assessed by CD4(+) T-cell depletion. The seven antigens provided robust additive protection when combined in four-antigen combinations. This study paves the way for the development of an effective anti-Chlamydia vaccine and provides a general approach for the discovery of vaccines against other intracellular pathogens.

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialBacterial ProteinsBacterial VaccinesBlotting, WesternB-LymphocytesCD4-Positive T-LymphocytesCell LineChlamydia InfectionsChlamydia muridarumChlamydia trachomatisFemaleHeLa CellsHumansImmune SeraAntibodies, BacterialAntigens, BacterialBacterial ProteinsBacterial VaccinesImmune SeraInterferon-gamma

Identifiers

PMID21628568
PMCPMC3116399
OpenAlexW2040455921

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.