Evidence map›Paper›PMID 24638855›Full record

ArticleCold Spring Harbor symposia on quantitative biology2013

The promised land of human immunology.

Laura F Su, Arnold Han, Helen M McGuire, David Furman, Evan W Newell, Mark M Davis

Abstract read
In one paragraph

Article in Cold Spring Harbor symposia on quantitative biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. An adjuvant-modulated vaccine response in human whole blood.Human vaccines & immunotherapeutics · 2017
    Article
  5. Article
  6. Article
  7. Review
  8. Anti-TNF therapy: past, present and future.International immunology · 2015
    Review
  9. 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

6 authors.

Laura F SuDivision of Rheumatology, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Arnold HanDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305.
Helen M McGuireDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305.
David FurmanDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305.
Evan W NewellSingapore Immunology Network, Agency for Science Technology and Research, Singapore 138648.
Mark M DavisDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305 Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, California 94305 Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305 mmdavis@stanford.edu.

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
NIAID NIH HHS U19 AI057229
6 · The paper itself

Abstract

Advances in technology and data analysis have made it possible to take a new look at human immunology. These advances run the gamut from systems biology approaches, which are likely in the vanguard of how we can start "to put the pieces together" of immune function, to a deeper understanding of specific diseases and vaccines and the immune repertoire. In our own experience, we have also found that asking simple questions about human immunity has often given us very surprising answers, causing a rethink of established dogma. Thus, we have developed a new perspective on the nature of the αβ TCR repertoire and also the likely role of T-cell repertoire (TCR) cross-reactivity in generating T memory independent of specific antigen interactions. These findings show that human immunology is not just a necessary step for "translating" basic immunology to treat diseases or develop better vaccines, but is also an important complement to the inbred mouse model.

Indexed as

Immunologic TechniquesAnimalsCeliac DiseaseFemaleHumansImmunologic MemoryInfluenza, HumanInfluenza VaccinesMaleMiceOdds RatioPhenotypeReceptors, Antigen, T-Cell, alpha-betaSystems BiologyT-LymphocytesInfluenza VaccinesReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID24638855
PMCPMC4896736

What OpenQuestion holds

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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.