Evidence map›Paper›PMID 25011109›Full record

ArticleCell host & microbe2014

A BTLA-mediated bait and switch strategy permits Listeria expansion in CD8α(+) DCs to promote long-term T cell responses.

Xuanming Yang, Xunmin Zhang, Yonglian Sun, Tony Tu, May Lynne Fu, Mendy Miller, Yang-Xin Fu

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Sustained AhR activity programs memory fate of early effector CD8Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  2. CTLs: Killers of intracellular bacteria.Frontiers in cellular and infection microbiology · 2022
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
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 2 countries.

Xuanming YangDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Xunmin ZhangDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA; International joint Cancer Institute, The Second Military Medical University, Shanghai, 200433, China.
Yonglian SunDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Tony TuDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
May Lynne FuDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Mendy MillerDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA. Electronic address: mendy.miller@gmail.com.
Yang-Xin FuDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA. Electronic address: yfu@uchicago.edu.
University of Chicago · USSecond Military Medical University · CN

Funding

MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Synergy of Radiation and Immunotherapy: New ApproachesR01CA134563 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MALTER, JAMES S · 2010 to 2019
$3.4M
Novel therapeutic approaches to treating chronic hepatitis B virus infectionR01DK095962 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FU, YANG-XIN, SU, LISHAN · 2013 to 2016
$2.1M
Tumor Necrosis Superfamily Ligands and Lymphocytes Role in Liver RegenerationR01DK080736 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI ANDERS, ROBERT A. · 2010 to 2014
$1.7M
TNF family members for lymph angiogenesis and lymph node hypertrophyR01CA141975 · NCI · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2010 to 2014
$1.6M
The role of Id2 in gut innate lymphoid cellsR01DK100427 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI FU, YANG-XIN · 2014 to 2017
$1.4M
NCATS NIH HHS UL1 TR000430NCI NIH HHS CA141975NCI NIH HHS R01 CA134563NCI NIH HHS R01 CA141975NIDDK NIH HHS DK080736NIDDK NIH HHS R01 DK080736NIDDK NIH HHS R01 DK095962NIDDK NIH HHS R01 DK100427NIGMS NIH HHS T32 GM007281
6 · The paper itself

Abstract

Listeria monocytogenes infected CD8α(+) DCs in the spleen are essential for CD8(+) T cell generation. CD8α(+) DCs are also necessary for Listeria expansion and dissemination within the host. The mechanisms that regulate CD8α(+) DCs to allow Listeria expansion are unclear. We find that activating the B and T lymphocyte attenuator (BTLA), a coinhibitory receptor for T cells, suppresses, while blocking BTLA enhances, both the primary and memory CD8 T cell responses against Listeria. Btla(-/-) mice have lower effector and memory CD8(+) T cells while paradoxically also being more resistant to Listeria. Although bacterial entry into Btla(-/-) CD8α(+) DCs is unaffected, Listeria fails to expand within these cells. BTLA signaling limits Fas/FasL-mediated suppression of Listeria expansion within CD8α(+) DCs to more effectively alert adaptive immune cells. This study uncovers a BTLA-mediated strategy used by the host that permits Listeria proliferation to enable increasing T cell responses for long-term protection.

Indexed as

Host-Pathogen InteractionsAnimalsCD8 AntigensDendritic CellsListeria monocytogenesMiceMice, KnockoutReceptors, ImmunologicT-LymphocytesBTLA protein, mouseCD8 AntigensReceptors, Immunologic

Identifiers

PMID25011109
PMCPMC4144681
OpenAlexW2043019041

What OpenQuestion holds

Textmetadata
LicenceTDM
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.