Evidence map›Paper›PMID 27875529›Full record

ArticlePLoS neglected tropical diseases2016

CD4+ T Cells Are as Protective as CD8+ T Cells against Rickettsia typhi Infection by Activating Macrophage Bactericidal Activity.

Kristin Moderzynski, Stefanie Papp, Jessica Rauch, Liza Heine, Svenja Kuehl, Ulricke Richardt, Bernhard Fleischer, Anke Osterloh

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  5. Review
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  7. Review
  8. Article
  9. Review
  10. The neglected challenge: Vaccination against rickettsiae.PLoS neglected tropical diseases · 2020
    Review
  11. Review
  12. Article
  13. Article
  14. Typhus Group Rickettsiosis, Germany, 2010-2017Emerging infectious diseases · 2018
    Article
  15. Review
  16. Article
  17. 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

8 authors at 2 institutions in 1 country.

Kristin ModerzynskiDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Stefanie PappDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Jessica RauchDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Liza HeineDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Svenja KuehlDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Ulricke RichardtDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Bernhard FleischerDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Anke OsterlohDepartment of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Bernhard Nocht Institute for Tropical Medicine · DEUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rickettsia typhi is an intracellular bacterium that causes endemic typhus, a febrile disease that can be fatal due to complications including pneumonia, hepatitis and meningoencephalitis, the latter being a regular outcome in T and B cell-deficient C57BL/6 RAG1-/- mice upon Rickettsia typhi infection. Here, we show that CD4+ TH1 cells that are generated in C57BL/6 mice upon R. typhi infection are as protective as cytotoxic CD8+ T cells. CD4+- as well as CD8+-deficient C57BL/6 survived the infection without showing symptoms of disease at any point in time. Moreover, adoptively transferred CD8+ and CD4+ immune T cells entered the CNS of C57BL/6 RAG1-/- mice with advanced infection and both eradicated the bacteria. However, immune CD4+ T cells protected only approximately 60% of the animals from death. They induced the expression of iNOS in infiltrating macrophages as well as in resident microglia in the CNS which can contribute to bacterial killing but also accelerate pathology. In vitro immune CD4+ T cells inhibited bacterial growth in infected macrophages which was in part mediated by the release of IFNγ. Collectively, our data demonstrate that CD4+ T cells are as protective as CD8+ T cells against R. typhi, provided that CD4+ TH1 effector cells are present in time to support bactericidal activity of phagocytes via the release of IFNγ and other factors. With regard to vaccination against TG Rickettsiae, our findings suggest that the induction of CD4+ TH1 effector cells is sufficient for protection.

Indexed as

Adoptive TransferAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleHumansMacrophagesMiceMice, Inbred C57BLRickettsia typhiTh1 CellsTyphus, Endemic Flea-Borne

Identifiers

PMID27875529
PMCPMC5119731
OpenAlexW2552653660

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.