Evidence map›Paper›PMID 16299294›Full record

ArticleInfection and immunity2005

Essential role for humoral immunity during Ehrlichia infection in immunocompetent mice.

Eric Yager, Constantine Bitsaktsis, Bisweswar Nandi, Jere W McBride, Gary Winslow

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Antigen-Specific CD4Frontiers in immunology · 2018
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Human ehrlichiosis and anaplasmosis.Clinics in laboratory medicine · 2010
    Review
  18. Review
  19. Article
  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

5 authors at 4 institutions in 1 country.

Eric YagerThe Department of Biomedical Sciences, School of Public Health, University at Albany, Albany, New York 12201-0509, USA.
Constantine Bitsaktsis
Bisweswar Nandi
Jere W McBride
Gary Winslow
New York State Department of Health · USThe University of Texas Medical Branch at Galveston · USUniversity at Albany, State University of New York · USWadsworth Center · US

Funding

Antibody mediated intracellular bacterial eliminationR01AI047963 · NIAID · WADSWORTH CENTER · PI WINSLOW, GARY M. · 2002 to 2006
$1.4M
NIAID NIH HHS R01 AI047963NIAID NIH HHS R01 AI47963
6 · The paper itself

Abstract

Although cellular immunity is essential for host defense during intracellular bacterial infections, humoral immunity can also play a significant role in host defense during infection by some intracellular bacteria, including the ehrlichiae. Antibodies can protect susceptible SCID mice from fatal Ehrlichia chaffeensis infection, an observation that has been hypothesized to involve the opsonization of bacteria released from host cells. To determine whether humoral immunity plays an essential role during ehrlichia infection in immunocompetent mice, we utilized a murine model of fatal monocytotropic ehrlichiosis caused by Ixodes ovatus ehrlichia. Mice lacking either B cells or FcgammaRI were unable to resolve a low-dose (sublethal) I. ovatus ehrlichia infection, which suggested that humoral immunity is essential for resistance. Polyclonal sera generated in I. ovatus ehrlichia-infected mice recognized a conserved ehrlichia outer membrane protein and, when administered to infected mice, caused a significant decrease in bacterial infection. Mice experimentally depleted of complement, or deficient for complement receptors 1 and 2, were also susceptible to sublethal I. ovatus ehrlichia infection, as were mice that lacked the phox91 subunit of NADPH oxidase. The data are consistent with a mechanism whereby bacteria released from infected cells are lysed directly by complement or undergo antibody-mediated FcgammaR-dependent phagocytosis and subsequent exposure to reactive oxygen intermediates. The findings suggest mechanisms whereby antibodies contribute to immunity against intracellular bacteria in immunocompetent mice.

Indexed as

Ehrlichia chaffeensisAnimalsAntibodies, BacterialAntibody FormationB-LymphocytesComplement System ProteinsEhrlichiosisImmune SeraImmunocompetenceIxodesMiceMice, SCIDNADPH OxidasesReactive Oxygen SpeciesReceptors, ComplementReceptors, Complement 3dAntibodies, BacterialComplement System ProteinsFcgr1 protein, mouseImmune SeraNADPH OxidasesReactive Oxygen SpeciesReceptors, ComplementReceptors, Complement 3dReceptors, IgG

Identifiers

PMID16299294
PMCPMC1307037
OpenAlexW2149376869

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.