Evidence map›Paper›PMID 9989985›Full record

ArticleThe Journal of experimental medicine1999

T cell affinity maturation by selective expansion during infection.

D H Busch, E G Pamer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

170 citing papers in PubMed, 417 citations in OpenAlex.

  1. Trial
  2. Clonal selection of somatic mutations shapes NK cell memory.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
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  6. Article
  7. Article
  8. A pain from the nose to the head: neurological commitment during long COVID.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Low-affinity CD8American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Development of Cancer Immunotherapies.Cancer treatment and research · 2022
    Article

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

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

2 authors at 1 institution in 1 country.

D H BuschSections of Infectious Diseases and Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06511, USA.
E G Pamer
Yale University · US

Funding

CC-chemokines in Listeria infection.R37AI039031 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI PAMER, ERIC G. · 2007 to 2016
$4.5M
Inflammation and T cell immunity to ListeriaR01AI039031 · NIAID · YALE UNIVERSITY · PI PAMER, ERIC G · 1996 to 2006
$1.9M
CYTOTOXIC T LYMPHOCYTE RESPONSE TO BACTERIAL INFECTIONR29AI033143 · NIAID · YALE UNIVERSITY · PI PAMER, ERIC G · 1994 to 1997
–
NIAID NIH HHS AI33143NIAID NIH HHS AI39031NIAID NIH HHS R01 AI039031NIAID NIH HHS R37 AI039031
6 · The paper itself

Abstract

T lymphocyte recognition of infected cells is mediated by T cell receptors (TCRs) interacting with their ligands, self-major histocompatibility complex (MHC) molecules complexed with pathogen-derived peptides. Serial TCR interactions with potentially small numbers of MHC/ peptide complexes on infected cells transmit signals that result in T lymphocyte expansion and activation of effector functions. The impact of TCR affinity for MHC/peptide complexes on the rate or extent of in vivo T cell expansion is not known. Here we show that in vivo expansion of complex T cell populations after bacterial infection is accompanied by an increase in their overall affinity for antigen. T cell populations that have undergone additional rounds of in vivo expansion express a narrower range of TCRs, have increased sensitivity for antigen in cytotoxic T lymphocyte assays, and bind MHC/peptide complexes with greater affinity. The selective expansion of higher affinity T cells provides an in vivo mechanism for optimizing the early detection of infected cells.

Indexed as

Bacterial ToxinsAnimalsAntigens, BacterialCell DifferentiationCell DivisionCells, CulturedGene Rearrangement, beta-Chain T-Cell Antigen ReceptorH-2 AntigensHeat-Shock ProteinsHemolysin ProteinsImmunization, SecondaryImmunologic MemoryListeria monocytogenesListeriosisMiceMice, Inbred BALB CAntigens, BacterialBacterial ToxinsH-2 AntigensH-2K(K) antigenHeat-Shock ProteinsHemolysin ProteinshlyA protein, Listeria monocytogenesReceptors, Antigen, T-Cell

Identifiers

PMID9989985
PMCPMC2192934
OpenAlexW2058634008

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.