Evidence map›Paper›PMID 9151711›Full record

ArticleThe Journal of experimental medicine1997

Degradation of T cell receptor (TCR)-CD3-zeta complexes after antigenic stimulation.

S Valitutti, S Müller, M Salio, A Lanzavecchia

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
–field-weighted citation impact
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

121 citing papers in PubMed.

  1. Trial
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  13. Proteostasis of immune checkpoint receptors.The Biochemical journal · 2025
    Review
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  19. Article
  20. Article

61 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

S ValituttiBasel Institute for Immunology, CH-4005, Basel, Switzerland.
S Müller
M Salio
A Lanzavecchia

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell activation by specific antigen results in a rapid and long-lasting downregulation of triggered T cell receptors (TCRs). In this work, we investigated the fate of downregulated TCR- CD3-zeta complexes. T cells stimulated by peptide-pulsed antigen-presenting cells (APCs) undergo an antigen dose-dependent decrease of the total cellular content of TCR-beta, CD3-epsilon, and zeta chains, as detected by FACS(R) analysis on fixed and permeabilized T-APC conjugates and by Western blot analysis on cell lysates. The time course of CD3-zeta chain consumption overlaps with that of TCR downregulation, indicating that internalized TCR-CD3 complexes are promptly degraded. Inhibitors of lysosomal function (bafilomycin A1, folimycin) markedly reduced zeta chain degradation, leading to the accumulation of zeta chain in large Lamp1(+) vesicles. These results indicate that in T cell-APC conjugates, triggered TCRs are rapidly removed from the cell surface and are degraded in the lysosomal compartment.

Indexed as

Lymphocyte ActivationMacrolidesAmino Acid SequenceAnti-Bacterial AgentsAntigen-Presenting CellsAntigensCalciumClone CellsDown-RegulationEnzyme InhibitorsFlow CytometryHumansInterferon-gammaKineticsLysosomesPeptide FragmentsAnti-Bacterial AgentsAntigensbafilomycin A1Calciumconcanamycin AEnzyme InhibitorsInterferon-gammaMacrolidesPeptide FragmentsProton-Translocating ATPasesReceptor-CD3 Complex, Antigen, T-CellTetanus Toxin

Identifiers

PMID9151711
PMCPMC2196323

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Registered trials

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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.