Evidence map›Paper›PMID 20190145›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Antigenic variation in Treponema pallidum: TprK sequence diversity accumulates in response to immune pressure during experimental syphilis.

Lorenzo Giacani, Barbara J Molini, Eric Y Kim, B Charmie Godornes, B Troy Leader, Lauren C Tantalo, Arturo Centurion-Lara, Sheila A Lukehart

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Pooled it
  2. Review
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  13. Proteomic analysis of theFrontiers in microbiology · 2024
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  16. Longitudinal Variations in theMicrobiology spectrum · 2023
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  17. Review
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  19. Review
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16 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Lorenzo GiacaniDepartment of Medicine, University of Washington, Seattle, WA 98104, USA.
Barbara J Molini
Eric Y Kim
B Charmie Godornes
B Troy Leader
Lauren C Tantalo
Arturo Centurion-Lara
Sheila A Lukehart
University of Washington · US

Funding

TREPONEMA PALLIDUM PATHOGENESIS ASSOCIATED MOLECULESR01AI042143 · NIAID · UNIVERSITY OF WASHINGTON · PI LUKEHART, SHEILA A. · 1998 to 2015
$5.4M
Project 4: Antigenic variation of TprKR01AI063940 · NIAID · UNIVERSITY OF WASHINGTON · PI LUKEHART, SHEILA A. · 2004 to 2013
$3.3M
NIAID NIH HHS R01 AI042143NIAID NIH HHS R01 AI063940NIAID NIH HHS R01 AI42143NIAID NIH HHS R01 AI63940
6 · The paper itself

Abstract

Pathogens that cause chronic infections often employ antigenic variation to evade the immune response and persist in the host. In Treponema pallidum (T. pallidum), the causative agent of syphilis, the TprK Ag undergoes variation of seven V regions (V1-V7) by nonreciprocal recombination of silent donor cassettes with the tprK expression site. These V regions are the targets of the host humoral immune response during experimental infection. The present study addresses the causal role of the acquired immune response in the selection of TprK variants in two ways: 1) by investigating TprK variants arising in immunocompetent versus immunosuppressed hosts; and 2) by investigating the effect of prior specific immunization on selection of TprK variants during infection. V region diversity, particularly in V6, accumulates more rapidly in immunocompetent rabbits than in pharmacologically immunosuppressed rabbits (treated with weekly injections of methylprednisolone acetate). In a complementary experiment, rabbits preimmunized with V6 region synthetic peptides had more rapid accumulation of V6 variant treponemes than control rabbits. These studies demonstrate that the host immune response selects against specific TprK epitopes expressed on T. pallidum, resulting in immune selection of new TprK variants during infection, confirming a role for antigenic variation in syphilis.

Indexed as

Amino Acid SequenceAnimalsAntibodies, BacterialAntigenic VariationAntigens, BacterialBacterial ProteinsBase SequenceDisease Models, AnimalMolecular Sequence DataPorinsRabbitsRecombination, GeneticReverse Transcriptase Polymerase Chain ReactionRNA, MessengerSyphilisTreponema pallidumAntibodies, BacterialAntigens, BacterialBacterial Proteinsmajor outer sheath protein, TreponemaPorinsRNA, Messenger

Identifiers

PMID20190145
PMCPMC3042355
OpenAlexW2167443134

What OpenQuestion holds

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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.