Evidence map›Paper›PMID 15845516›Full record

ArticleInfection and immunity2005

A monoclonal antibody that conveys in vitro killing and partial protection in experimental syphilis binds a phosphorylcholine surface epitope of Treponema pallidum.

David R Blanco, Cheryl I Champion, Alek Dooley, David L Cox, Julian P Whitelegge, Kym Faull, Michael A Lovett

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. CDC Laboratory Recommendations for Syphilis Testing, United States, 2024.MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Biological basis for syphilis.Clinical microbiology reviews · 2006
    Review
  19. 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

7 authors at 3 institutions in 1 country.

David R BlancoA2-087G Center for Health Sciences, UCLA School of Medicine, Los Angeles, CA 90095, USA. dblanco@mednet.ucla.edu
Cheryl I Champion
Alek Dooley
David L Cox
Julian P Whitelegge
Kym Faull
Michael A Lovett
Office of Infectious Diseases · USCenters for Disease Control and Prevention · USUniversity of California, Los Angeles · US

Funding

IMMUNE MECHANISMS IN EXPERIMENTAL SYPHILISR01AI012601 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LOVETT, MICHAEL A. · 1986 to 2004
$2.3M
Immune Mechanisms in Experimental SyphilisR56AI012601 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LOVETT, MICHAEL A. · 2005 to 2005
$460k
GENETICS OF TREPONEMA PALLIDUM PATHOGENICITYR01AI021352 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LOVETT, MICHAEL A. · 1985 to 1995
–
NIAID NIH HHS AI-12601NIAID NIH HHS AI21352NIAID NIH HHS R01 AI012601NIAID NIH HHS R56 AI012601
6 · The paper itself

Abstract

Immunization with purified Treponema pallidum outer membrane vesicles (OMV) has previously resulted in high-titer complement-dependent serum bactericidal activity. In this study, OMV immunization resulted in the isolation of a monoclonal antibody, M131, with complement-dependent killing activity. Passive immunization of rabbits with M131 administered intravenously conferred significant immunity demonstrated by the failure of syphilitic lesions to appear at 29% of intradermal challenge sites (7/24) and a mean delay of approximately 8 days to lesion appearance at the remaining sites (17/24). M131 not only bound to OMV and to the surfaces of intact motile T. pallidum cells but also bound to organisms whose outer membranes were removed, indicating both surface and subsurface locations for the killing target. This target was determined to be a T. pallidum lipid. Lipid extracted from T. pallidum and made into liposomes bound M131. Reverse-phase high-pressure liquid chromatography separation and fraction collection mass spectrometry (LC-MS+) of T. pallidum lipid showed that the target of M131 was phosphorylcholine. M131 binding required both liposome formation and a critical concentration of phospholipid containing phosphorylcholine, suggesting that the epitope has both a conformational and a compositional requirement. M131 did not react with red blood cells, which have phosphorylcholine-containing lipids in their exterior membrane leaflets, or with Venereal Disease Research Laboratory antigen that also contains phosphorylcholine, further indicating the specificity of M131. This is the first physical demonstration of an antigen on the T. pallidum surface and indication that such a surface antigen can be a target of immunity.

Indexed as

AnimalsAntibodies, MonoclonalAntibody SpecificityAntigens, SurfaceEpitopesHumansImmunization, PassiveMiceMice, Inbred BALB CPhosphorylcholinePolymerase Chain ReactionRabbitsSyphilisTreponema pallidumAntibodies, MonoclonalAntigens, SurfaceEpitopesPhosphorylcholine

Identifiers

PMID15845516
PMCPMC1087381
OpenAlexW2104764812

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.