Evidence map›Paper›PMID 29135332›Full record

ArticleHuman vaccines & immunotherapeutics2018

Antibodies to PcpA and PhtD protect mice against Streptococcus pneumoniae by a macrophage- and complement-dependent mechanism.

Lucian Visan, Nicolas Rouleau, Emilie Proust, Loïc Peyrot, Arnaud Donadieu, Martina Ochs

Abstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. The truncated major pilin subunit SBP2' contributes toApplied and environmental microbiology · 2026
    Article
  2. Review
  3. Article
  4. Human vaccines & immunotherapeutics · 2025
    Review
  5. Article
  6. Novel processes to obtain pneumococcal surface proteins for vaccines.Applied microbiology and biotechnology · 2025
    Review
  7. Review
  8. Article
  9. Alternate Antimicrobial Therapies and Their Companion Tests.Diagnostics (Basel, Switzerland) · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Diverse Mechanisms of Protective Anti-Pneumococcal Antibodies.Frontiers in cellular and infection microbiology · 2022
    Review
  17. Article
  18. Review
  19. Review
  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

6 authors.

Lucian Visana Sanofi Pasteur , Research & Non Clinical Safety Department , Marcy l'Etoile , France.
Nicolas Rouleaua Sanofi Pasteur , Research & Non Clinical Safety Department , Marcy l'Etoile , France.
Emilie Prousta Sanofi Pasteur , Research & Non Clinical Safety Department , Marcy l'Etoile , France.
Loïc Peyrota Sanofi Pasteur , Research & Non Clinical Safety Department , Marcy l'Etoile , France.
Arnaud Donadieua Sanofi Pasteur , Research & Non Clinical Safety Department , Marcy l'Etoile , France.
Martina Ochsa Sanofi Pasteur , Research & Non Clinical Safety Department , Marcy l'Etoile , France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently marketed Streptococcus pneumoniae (Spn) vaccines, which contain polysaccharide capsular antigens from the most common Spn serotypes, have substantially reduced pneumococcal disease rates but have limited coverage. A trivalent pneumococcal protein vaccine containing pneumococcal choline-binding protein A (PcpA), pneumococcal histidine triad protein D (PhtD), and detoxified pneumolysin is being developed to provide broader, cross-serotype protection. Antibodies against detoxified pneumolysin protect against bacterial pneumonia by neutralizing Spn-produced pneumolysin, but how anti-PhtD and anti-PcpA antibodies protect against Spn has not been established. Here, we used a murine passive protection sepsis model to investigate the mechanism of protection by anti-PhtD and anti-PcpA antibodies. Depleting complement using cobra venom factor eliminated protection by anti-PhtD and anti-PcpA monoclonal antibodies (mAbs). Consistent with a requirement for complement, complement C3 deposition on Spn in vitro was enhanced by anti-PhtD and anti-PcpA mAbs and by sera from PhtD- and PcpA-immunized rabbits and humans. Moreover, in the presence of complement, anti-PhtD and anti-PcpA mAbs increased uptake of Spn by human granulocytes. Depleting neutrophils using anti-Ly6G mAbs, splenectomy, or a combination of both did not affect passive protection against Spn, whereas depleting macrophages using clodronate liposomes eliminated protection. These results suggest anti-PhtD and anti-PcpA antibodies induced by pneumococcal protein vaccines protect against Spn by a complement- and macrophage-dependent opsonophagocytosis.

Indexed as

AnimalsBacterial ProteinsCarrier ProteinsComplement System ProteinsImmunity, CellularIntracellular Signaling Peptides and ProteinsMacrophagesMicePneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniaeVaccinationBacterial ProteinsCarrier ProteinsComplement System ProteinsIntracellular Signaling Peptides and ProteinsPcpA protein, StreptococcusPneumococcal VaccinesantibodycomplementmacrophageneutrophilopsonophagocytosisphagocytosisStreptococcus pneumoniaevaccination

Identifiers

PMID29135332
PMCPMC5806646

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.