Evidence map›Paper›PMID 11353822›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

CD8+ T cells control the TH phenotype of MBP-reactive CD4+ T cells in EAE mice.

H Jiang, N S Braunstein, B Yu, R Winchester, L Chess

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

52 citing papers in PubMed, 124 citations in OpenAlex.

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  10. Role of TRIF Small Interference RNA (siRNA) in Chronic Experimental Allergic Encephalomyelitis (EAE).Medical science monitor : international medical journal of experimental and clinical research · 2015
    Article
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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

5 authors at 1 institution in 1 country.

H JiangCollege of Physicians and Surgeons, Columbia University, New York, NY 10032, USA. hj4@columbia.edu
N S Braunstein
B Yu
R Winchester
L Chess
Columbia University · US

Funding

CD8+ T CELL RECOGNITION OF TH1 AND TH2R01AI044927 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JIANG, HONG · 1999 to 2003
$1.0M
IMMUNE RESPONSES BY TCR VB SPECIFIC CD8 T CELLSR29AI039630 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JIANG, HONG · 1996 to 2000
$121k
SMALL INSTRUMENTATION PROGRAMS15AI030675 · NIAID · UNIVERSITY OF NEW MEXICO · PI SCALETTI, JOSEPH V · 1990 to 1990
–
NIAID NIH HHS AI30675NIAID NIH HHS AI39630NIAID NIH HHS AI44927
6 · The paper itself

Abstract

Trimolecular interactions between the T cell antigen receptor and MHC/peptide complexes, together with costimulatory molecules and cytokines, control the initial activation of naive T cells and determine whether the helper precursor cell differentiates into either T helper (TH)1 or TH2 effector cells. We now present evidence that regulatory CD8(+) T cells provide another level of control of TH phenotype during further evolution of immune responses. These regulatory CD8(+) T cells are induced by antigen-triggered CD4(+) TH1 cells during T cell vaccination and, in vitro, distinguish mature TH1 from TH2 cells in a T cell antigen receptor Vbeta-specific and Qa-1-restricted manner. In vivo, protection from experimental autoimmune encephalomyelitis (EAE) induced by T cell vaccination depends on CD8(+) T cells, and myelin basic protein-reactive TH1 Vbeta8(+) clones, but not TH2 Vbeta8(+) clones, used as vaccine T cells, protect animals from subsequent induction of EAE. Moreover, in vivo depletion of CD8(+) T cells during the first episode of EAE results in skewing of the TH phenotype toward TH1 upon secondary myelin basic protein stimulation. These data provide evidence that CD8(+) T cells control autoimmune responses, in part, by regulating the TH phenotype of self-reactive CD4(+) T cells.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesEncephalomyelitis, Autoimmune, ExperimentalFemaleHistocompatibility Antigens Class IHybridomasImmunophenotypingInterferon-gammaInterleukin-2Interleukin-4Lymphocyte ActivationMiceMyelin Basic ProteinPeptide FragmentsReceptors, Antigen, T-Cell, alpha-betaHistocompatibility Antigens Class IInterferon-gammaInterleukin-2Interleukin-4Myelin Basic Proteinmyelin basic protein 1-9Peptide FragmentsQ surface antigensReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID11353822
PMCPMC33463
OpenAlexW2113883987

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.