Evidence map›Paper›PMID 11260325›Full record

ArticleImmunology2001

Immunological memory in B-cell-deficient mice conveys long-lasting protection against genital tract infection with Chlamydia trachomatis by rapid recruitment of T cells.

M Johansson, N Lycke

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 41 citations in OpenAlex.

  1. Reduction ofVaccine: X · 2023
    Article
  2. Genital Infiltrations of CD4Frontiers in microbiology · 2019
    Article
  3. Article
  4. B Cell Depletion With an Anti-CD20 Antibody Enhances Alloreactive Memory T Cell Responses After Transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Article
  5. Review
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  9. Article
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  11. Review
  12. B cells help alloreactive T cells differentiate into memory T cells.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2010
    Article
  13. Article
  14. Requirement of B cells for generating CD4+ T cell memory.Journal of immunology (Baltimore, Md. : 1950) · 2009
    Article
  15. Article
  16. 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

2 authors at 1 institution in 1 country.

M JohanssonDepartment of Medical Microbiology and Immunology, University of Göteborg, Göteborg, Sweden.
N Lycke
University of Gothenburg · SE

Funding

Dissecting basal ganglia circuit mechanisms underlying instrumental learningR01DA040701 · NIDA · DUKE UNIVERSITY · PI Henry Yin · 2016 to 2026
$3.6M
CHOLERA TOXIN--A MUCOSAL ADJUVANT, MECHANISMS &IMMUNITYR01AI040701 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI NEDRUD, JOHN G. · 1997 to 1999
–
NIAID NIH HHS R01 AI40701NIDA NIH HHS R01 DA040701
6 · The paper itself

Abstract

The role of antibodies and antigen deposition for the development of immunological memory has been incompletely investigated. We addressed whether long-term protection and T-cell memory can be stimulated against a genital tract infection with human Chlamydia trachomatis serovar D in B-cell-deficient (muMT) mice. At 6 months following a primary infection with C. trachomatis, both muMT and wild-type (WT) mice exhibited strong and comparable protection against reinfection. Evidence of long-lasting CD4+ T-cell memory was found in both muMT and WT mice, typified by comparable delayed-type hypersensitivity (DTH) reactions against chlamydial antigens. No bacterial or chlamydial DNA was found in the genital tract of muMT memory mice, suggesting that immunological memory was maintained in the absence of antigen. Whereas few T cells were present in the genital tract of memory mice, rapid recruitment of CD4+, and some CD8+, T cells into the genital tract tissue was observed after challenge with live bacteria. Accumulation of T cells in the genital tract was preceded by a short transient infection of similar magnitude in both muMT and WT memory mice, arguing against a long-term protective role of local antibodies. The rapid recruitment of CD4+ T cells into the genital tract was associated with a transient detection of interferon-gamma (IFN-gamma) mRNA in the genital tract in chlamydia-immune memory mice, which was not found in naïve, challenged mice. Thus, long-term protection in the genital tract against C. trachomatis infection is conveyed by IFN-gamma-producing CD4+ memory T cells, which appear to be maintained in the absence of antibodies and local antigen deposition.

Indexed as

Immunologic MemoryAnimalsAntibodies, BacterialAntigens, BacterialB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChlamydia InfectionsChlamydia trachomatisFemaleGenital Diseases, FemaleGenitalia, FemaleImmunity, CellularImmunoenzyme TechniquesInterferon-gammaMiceAntibodies, BacterialAntigens, BacterialInterferon-gamma

Identifiers

PMID11260325
PMCPMC1783171
OpenAlexW2036845250

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.