Evidence map›Paper›PMID 8879221›Full record

ArticleThe Journal of experimental medicine1996

Beta 2-microglobulin-dependent T cells are dispensable for allergen-induced T helper 2 responses.

Y Zhang, K H Rogers, D B Lewis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
7.7field-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

29 citing papers in PubMed, 100 citations in OpenAlex.

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  17. Requirement for natural killer T (NKT) cells in the induction of allograft tolerance.Proceedings of the National Academy of Sciences of the United States of America · 2001
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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

3 authors at 1 institution in 1 country.

Y ZhangDepartment of Pediatrics, University of Washington, Seattle 98195, USA.
K H Rogers
D B Lewis
University of Washington · US

Funding

MECHANISM OF OSTEOPOROSIS IN IL4 TRANSGENIC MICER01AR041657 · NIAMS · UNIVERSITY OF WASHINGTON · PI LEWIS, DAVID BRAM · 1992 to 1995
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ROLE OF 5-LIPOXYGENASE PRODUCTS IN AIRWAY INFLAMMATIONU01AI034578 · NIAID · UNIVERSITY OF WASHINGTON · PI HARLAN, JOHN MARSHALL · 1993 to 1996
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NIAID NIH HHS AI-24940NIAID NIH HHS AI-34578NIAMS NIH HHS AR-41657
6 · The paper itself

Abstract

CD4+ and CD8+ alpha/beta+ T cells of the T helper cell (Th)2 phenotype produce the cytokines IL-4, IL-5, and IL-13 that promote IgE production and eosinophilic inflammation. IL-4 may play an important role in mediating the differentiation of antigenically naive alpha/beta+ T cells into Th2 cells. Murine NK1.1+ (CD4+ or CD4-CD8-) alpha/beta+ T cells comprise a beta 2-microglobulin (beta 2m)-dependent cell population that rapidly produces IL-4 after cell activation in vitro and in vivo and has been proposed as a source of IL-4 for Th2 cell differentiation. alpha/beta+ CD8+ T cells, most of which require beta 2m for their development, have also been proposed as positive regulators of allergen-induced Th2 responses. We tested whether beta 2m-dependent T cells were essential for Th2 cell-mediated allergic reactions by treating wild-type, beta 2m-deficient (beta 2m -/-), and IL-4-deficient (IL-4 -/-) mice of the C57BL/6 genetic background with ovalbumin (OVA), using a protocol that induces robust allergic pulmonary disease in wild-type mice. OVA-treated beta 2m -/- mice had circulating levels of total and OVA-specific IgE, pulmonary eosinophilia, and expression of IL-4, IL-5, and IL-13 mRNA in bronchial lymph node tissue similar to that of OVA-treated wild-type mice. In contrast, these responses in OVA-treated IL-4 -/- mice were all either undetectable or markedly reduced compared with wild-type mice, confirming that IL-4 was required in this allergic model. These results indicate that the NK1.1+ alpha/beta+ T cell population, as well as other beta 2m-dependent populations, such as most peripheral alpha/beta+ CD8+ T cells, are dispensable for the Th2 pulmonary response to protein allergens.

Indexed as

AllergensAnimalsAntigensAntigens, LyAntigens, Surfacebeta 2-MicroglobulinBronchoalveolar Lavage FluidImmunoglobulin EInterleukin-13Interleukin-4Interleukin-5Lectins, C-TypeLymph NodesMiceMice, Inbred C57BLMice, Mutant StrainsAllergensAntigensAntigens, LyAntigens, Surfacebeta 2-MicroglobulinImmunoglobulin EInterleukin-13Interleukin-4Interleukin-5Klrb1c protein, mouseLectins, C-TypeNK Cell Lectin-Like Receptor Subfamily BOvalbuminProteins

Identifiers

PMID8879221
PMCPMC2192811
OpenAlexW2112495824

What OpenQuestion holds

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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.