Evidence map›Paper›PMID 21881204›Full record

ArticleThe Journal of clinical investigation2011

Protective antiviral antibody responses in a mouse model of influenza virus infection require TACI.

Amaya I Wolf, Krystyna Mozdzanowska, William J Quinn, Michele Metzgar, Katie L Williams, Andrew J Caton, Eric Meffre, Richard J Bram, Loren D Erickson, David Allman and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 62 citations in OpenAlex.

  1. B cell-intrinsic CXCR3 drives efficient generation of ectopic pulmonary germinal center responses to influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Frontiers in immunology · 2021
    Article
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  15. Article
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  18. The Multifaceted B Cell Response to Influenza Virus.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Review
  19. TACI Contributes toFrontiers in immunology · 2018
    Article
  20. 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

12 authors at 5 institutions in 1 country.

Amaya I WolfThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
Krystyna Mozdzanowska
William J Quinn
Michele Metzgar
Katie L Williams
Andrew J Caton
Eric Meffre
Richard J Bram
Loren D Erickson
David Allman
Michael P Cancro
Jan Erikson
The Wistar Institute · USUniversity of Pennsylvania · USMayo Clinic · USUniversity of Virginia · USYale University · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Regulation of IgA class switching in the intestinal mucosaP01AI061093 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CUNNINGHAM-RUNDLES, CHARLOTTE · 2004 to 2021
$29.8M
TRAINING PROGRAM IN BASIC CANCER RESEARCHT32CA009171 · NCI · WISTAR INSTITUTE · PI Alessandro Gardini · 1985 to 2026
$15.3M
The Impact of Bacterial Co-Infectin on Respiratory Virus-Specific T cell ResponseU19AI083022 · NIAID · WISTAR INSTITUTE · PI ERIKSON, JAN S. · 2009 to 2013
$10.7M
Loss of B Cell Tolerance in Rheumatoid ArthritisR01AI071087 · NIAID · YALE UNIVERSITY · PI MEFFRE, ERIC · 2006 to 2016
$4.3M
Immune System Development and RegulationT32AI055428 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, OLIVER, PAULA MARIA · 2003 to 2025
$4.2M
MECHANISMS OF LYMPHOID LINEAGE COMMITMENTR01AI052861 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M · 2002 to 2013
$3.6M
Pathways of plasma cell differentiation in autoimmunityR01AI093722 · NIAID · UNIVERSITY OF VIRGINIA · PI ERICKSON, LOREN D · 2012 to 2016
$2.0M
ROLE OF BLYS IN PERIPHERAL B CELL SELECTION AND SURVIVALR01AI054488 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI CANCRO, MICHAEL PAUL · 2004 to 2008
$1.9M
NCI NIH HHS P30 CA010815NCI NIH HHS P30 CA10815NCI NIH HHS T32 CA009171NCI NIH HHS T32 CA09171-32NIAID NIH HHS AI055428NIAID NIH HHS AI061093NIAID NIH HHS AI071087NIAID NIH HHS AI52861NIAID NIH HHS P01 AI061093NIAID NIH HHS R01 AI052861NIAID NIH HHS R01 AI054488NIAID NIH HHS R01 AI071087NIAID NIH HHS R01 AI093722NIAID NIH HHS T32 AI055428NIAID NIH HHS U19 AI083022NIA NIH HHS AG58066
6 · The paper itself

Abstract

Antiviral Abs, for example those produced in response to influenza virus infection, are critical for virus neutralization and defense against secondary infection. While the half-life of Abs is short, Ab titers can last a lifetime due to a subset of the Ab-secreting cells (ASCs) that is long lived. However, the mechanisms governing ASC longevity are poorly understood. Here, we have identified a critical role for extrinsic cytokine signals in the survival of respiratory tract ASCs in a mouse model of influenza infection. Irradiation of mice at various time points after influenza virus infection markedly diminished numbers of lung ASCs, suggesting that they are short-lived and require extrinsic factors in order to persist. Neutralization of the TNF superfamily cytokines B lymphocyte stimulator (BLyS; also known as BAFF) and a proliferation-inducing ligand (APRIL) reduced numbers of antiviral ASCs in the lungs and bone marrow, whereas ASCs in the spleen and lung-draining lymph node were surprisingly unaffected. Mice deficient in transmembrane activator and calcium-modulator and cyclophilin ligand interactor (TACI), a receptor for BLyS and APRIL, mounted an initial antiviral B cell response similar to that generated in WT mice but failed to sustain protective Ab titers in the airways and serum, leading to increased susceptibility to secondary viral challenge. These studies highlight the importance of TACI signaling for the maintenance of ASCs and protection against influenza virus infection.

Indexed as

AnimalsAntibodies, ViralAntibody-Producing CellsB-Cell Activating FactorCD8-Positive T-LymphocytesCell SurvivalDisease Models, AnimalFemaleLungMaleMiceMice, Inbred C3HMice, KnockoutMice, TransgenicOrthomyxoviridae InfectionsSignal TransductionAntibodies, ViralB-Cell Activating FactorTnfrsf13b protein, mouseTnfsf13 protein, mouseTransmembrane Activator and CAML Interactor ProteinTumor Necrosis Factor Ligand Superfamily Member 13

Identifiers

PMID21881204
PMCPMC3195469
OpenAlexW2092047962

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.