Evidence map›Paper›PMID 30144035›Full record

ArticleImmunology2018

γδ T cells modulate humoral immunity against Plasmodium berghei infection.

Shin-Ichi Inoue, Mamoru Niikura, Hiroko Asahi, Yasushi Kawakami, Fumie Kobayashi

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Malaria: past, present, and future.Signal transduction and targeted therapy · 2025
    Review
  4. Article
  5. The function of γδ T cells in humoral immune responses.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. T cell-mediated immunity to malaria.Nature reviews. Immunology · 2019
    Review
  12. Interleukin (IL)-21 in Inflammation and Immunity During Parasitic Diseases.Frontiers in cellular and infection microbiology · 2019
    Review
  13. Review
  14. 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

5 authors at 2 institutions in 1 country.

Shin-Ichi InoueDivision of Immunology, Department of Molecular Microbiology and Immunology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.ORCID 0000-0003-1244-826X
Mamoru NiikuraDepartment of Infectious Diseases, Kyorin University School of Medicine, Tokyo, Japan.
Hiroko AsahiDepartment of Infectious Diseases, Kyorin University School of Medicine, Tokyo, Japan.
Yasushi KawakamiLaboratory of Parasitology, School of Life and Environmental Science, Azabu University, Kanagawa, Japan.
Fumie KobayashiDepartment of Infectious Diseases, Kyorin University School of Medicine, Tokyo, Japan.
Kyorin University · JPAzabu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is unclear whether γδ T cells are involved in humoral immunity against Plasmodium infection. Here, we show that B-cell-immunodeficient mice and γδ T-cell-deficient mice were incapable of protecting against Plasmodium berghei XAT parasites. γδ T-cell-deficient mice developed reduced levels of antigen-specific antibodies during the late phase of infection. The numbers of follicular helper T cells and germinal centre B cells in γδ T-cell-deficient mice were lower than in wild-type mice during the late phase of infection. Expression profiling of humoral immunity-related cytokines in γδ T cells showed that interleukin-21 (IL-21) and interferon-γ (IFN-γ) are increased during the early stage of infection. Furthermore, blockade of IL-21 and IFN-γ signalling during the early stage of infection led to reduction in follicular helper T cells and germinal centre B cells. γδ T-cell production of IL-21 and IFN-γ is crucial for the development and maintenance of follicular helper T cells and germinal centre B cells during the late phase of infection. Our data suggest that γδ T cells modulate humoral immunity against Plasmodium infection.

Indexed as

AnimalsCD4 Lymphocyte CountFemaleGerminal CenterImmunity, HumoralInterferon-gammaInterleukin-21InterleukinsMalariaMiceMice, Inbred C57BLMice, KnockoutPlasmodium bergheiReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocytes, Helper-InducerIFNG protein, mouseInterferon-gammaInterleukin-21InterleukinsReceptors, Antigen, T-Cell, gamma-deltahumoral immunitymalariaγδ T cells

Identifiers

PMID30144035
PMCPMC6231001
OpenAlexW2888727263

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.