Evidence map›Paper›PMID 17785819›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

The role of B cells in the development of CD4 effector T cells during a polarized Th2 immune response.

Qian Liu, Zhugong Liu, Cristina T Rozo, Hossein A Hamed, Farhang Alem, Joseph F Urban, William C Gause

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Anti-CD20 treatment attenuates Th2 cell responses: implications for the role of lung follicular mature B cells in the asthmatic mice.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Immune pathogenesis in pigeons during experimentalFrontiers in veterinary science · 2022
    Article
  7. Review
  8. B Cell IL-4 Drives Th2 ResponsesFrontiers in immunology · 2022
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. IL-4-producing B cells regulate T helper cell dichotomy in type 1- and type 2-controlled diseases.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  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

7 authors at 2 institutions in 1 country.

Qian LiuDepartment of Medicine, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark, NJ 07103, USA.
Zhugong Liu
Cristina T Rozo
Hossein A Hamed
Farhang Alem
Joseph F Urban
William C Gause
Rutgers, The State University of New Jersey · USBeltsville Human Nutrition Research Center · US

Funding

CYTOKINE GENE EXPRESSION DURING IN VIVO IMMUNE RESPONSER01AI031678 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI GAUSE, WILLIAM CLARK · 1994 to 2013
$4.2M
Gr-1+ cells and the response to nematode parasitesR01AI066188 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI GAUSE, WILLIAM CLARK · 2006 to 2010
$1.9M
NIAID NIH HHS AI31678NIAID NIH HHS R01 AI031678NIAID NIH HHS R01 AI066188
6 · The paper itself

Abstract

Previous studies have suggested that B cells promote Th2 cell development by inhibiting Th1 cell differentiation. To examine whether B cells are directly required for the development of IL-4-producing T cells in the lymph node during a highly polarized Th2 response, B cell-deficient and wild-type mice were inoculated with the nematode parasite, Nippostrongylus brasiliensis. On day 7, in the absence of increased IFN-gamma, IL-4 protein and gene expression from CD4 T cells in the draining lymph nodes were markedly reduced in B cell-deficient mice and could not be restored by multiple immunizations. Using a DO11.10 T cell adoptive transfer system, OVA-specific T cell IL-4 production and cell cycle progression, but not cell surface expression of early activation markers, were impaired in B cell-deficient recipient mice following immunization with N. brasiliensis plus OVA. Laser capture microdissection and immunofluorescent staining showed that pronounced IL-4 mRNA and protein secretion by donor DO11.10 T cells first occurred in the T cell:B cell zone of the lymph node shortly after inoculation of IL-4-/- recipients, suggesting that this microenvironment is critical for initial Th2 cell development. Reconstitution of B cell-deficient mice with wild-type naive B cells, or IL-4-/- B cells, substantially restored Ag-specific T cell IL-4 production. However, reconstitution with B7-1/B7-2-deficient B cells failed to rescue the IL-4-producing DO11.10 T cells. These results suggest that B cells, expressing B7 costimulatory molecules, are required in the absence of an underlying IFN-gamma-mediated response for the development of a polarized primary Ag-specific Th2 response in vivo.

Indexed as

Adoptive TransferAmino Acid SequenceAnimalsB-LymphocytesCD4-Positive T-LymphocytesCell DifferentiationEpitopes, T-LymphocyteMiceMice, Inbred BALB CMice, Mutant StrainsMice, TransgenicMolecular Sequence DataNippostrongylusOvalbuminPeptide FragmentsStrongylida InfectionsEpitopes, T-LymphocyteOVA 323-339OvalbuminPeptide Fragments

Identifiers

PMID17785819
PMCPMC2258088
OpenAlexW1897379845

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.