Evidence map›Paper›PMID 19251656›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Antigen-specific B-1a antibodies induced by Francisella tularensis LPS provide long-term protection against F. tularensis LVS challenge.

Leah E Cole, Yang Yang, Karen L Elkins, Ellen T Fernandez, Nilofer Qureshi, Mark J Shlomchik, Leonard A Herzenberg, Leonore A Herzenberg, Stefanie N Vogel

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

88 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. The immune response toFrontiers in microbiology · 2025
    Review
  7. Noncanonical B Cells: Characteristics of Uncharacteristic B Cells.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Microorganisms · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Purification and Immune Phenotyping of B-1 Cells from Body Cavities of Mice.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  17. Article
  18. Article
  19. Frontiers in cellular and infection microbiology · 2020
    Article
  20. Article

28 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

9 authors at 5 institutions in 1 country.

Leah E ColeDepartment of Microbiology and Immunology, University of Maryland, Baltimore, MD 21201, USA.
Yang Yang
Karen L Elkins
Ellen T Fernandez
Nilofer Qureshi
Mark J Shlomchik
Leonard A Herzenberg
Leonore A Herzenberg
Stefanie N Vogel
Stanford University · USCenter for Biologics Evaluation and Research · USUniversity of Maryland, Baltimore · USUniversity of Missouri–Kansas City · USYale University · US

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI LEVINE, MYRON MAX · 2003 to 2013
$91.5M
Murine Memory B Cell Development and FunctionR01AI043603 · NIAID · YALE UNIVERSITY · PI MARK J SHLOMCHIK · 1998 to 2026
$9.7M
DIFFERENTIATIVE SIGNALS FOR MACROPHAGE ACTIVATIONR37AI018797 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2000 to 2009
$5.3M
DIFFERENTIATIVE SIGNALS FOR MACROPHANGE ACTIVATIONR01AI018797 · NIAID · U.S. UNIFORMED SERVICES UNIV OF HLTH SCI · PI VOGEL, STEFANIE N. · 1985 to 2014
$3.8M
MECHANISMS INVOLVED IN THE SEPTIC SHOCK SYNDROMER01GM050870 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI QURESHI, NILOFER · 1994 to 2010
$3.4M
New perspective on innate antibodies in miceR01AI076434 · NIAID · STANFORD UNIVERSITY · PI HERZENBERG, LEONORE A. · 2009 to 2011
$1.1M
Murine Memory B Cell Development and FunctionR56AI043603 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHLOMCHIK, MARK J · 2016 to 2016
$609k
Differentiative Signals for Macrophage ActivationR56AI018797 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2015 to 2015
$506k
New Perspective on Innate Antibodies in MiceR56AI076434 · NIAID · STANFORD UNIVERSITY · PI HERZENBERG, LEONORE A. · 2008 to 2008
$409k
NIAID NIH HHS AI076434NIAID NIH HHS AI18797NIAID NIH HHS AI43603NIAID NIH HHS AI57168NIAID NIH HHS R01 AI018797NIAID NIH HHS R01 AI043603NIAID NIH HHS R01 AI076434NIAID NIH HHS R37 AI018797NIAID NIH HHS R56 AI018797NIAID NIH HHS R56 AI043603NIAID NIH HHS R56 AI076434NIAID NIH HHS U54 AI057168NIAID NIH HHS U54 AI157168NIAID NIH HHS Y01 AI006153NIAID NIH HHS Y1 AI-6153-01NIGMS NIH HHS GM50870NIGMS NIH HHS R01 GM050870
6 · The paper itself

Abstract

Francisella tularensis (Ft), a gram-negative intracellular bacterium, is the etiologic agent of tularemia. Infection of mice with <10 Ft Live Vaccine Strain (Ft LVS) organisms i.p. causes a lethal infection that resembles human tularemia. Here, we show that immunization with as little as 0.1 ng Ft LVS lipopolysaccharide (Ft-LPS), but not Ft lipid A, generates a rapid antibody response that protects wild-type (WT) mice against lethal Ft LVS challenge. Protection is not induced in Ft-LPS-immunized B cell-deficient mice (muMT or JhD), male xid mice, or Ig transgenic mice that produce a single IgH (not reactive with Ft-LPS). Focusing on the cellular mechanisms that underlie this protective response, we show that Ft-LPS specifically stimulates proliferation of B-1a lymphocytes that bind fluorochrome-labeled Ft-LPS and the differentiation of these cells to plasma cells that secrete antibodies specific for Ft-LPS. This exclusively B-1a antibody response is equivalent in WT, T-deficient (TCRalphabeta(-/-), TCRgammadelta(-/-)), and Toll-like receptor 4 (TLR4)-deficient (TLR4(-/-)) mice and thus is not dependent on T cells or typical inflammatory processes. Serum antibody levels peak approximately 5 days after Ft-LPS immunization and persist at low levels for months. Thus, immunization with Ft-LPS activates a rare population of antigen-specific B-1a cells to produce a persistent T-independent antibody response that provides long-term protection against lethal Ft LVS infection. These data support the possibility of creating effective, minimally invasive vaccines that can provide effective protection against pathogen invasion.

Indexed as

Antibody FormationAnimalsAntibodies, BacterialAntigens, BacterialBacterial VaccinesB-LymphocytesFrancisella tularensisLipopolysaccharidesLymphocyte ActivationMiceMice, KnockoutTularemiaAntibodies, BacterialAntigens, BacterialBacterial VaccinesLipopolysaccharides

Identifiers

PMID19251656
PMCPMC2657382
OpenAlexW2061545809

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.