Evidence map›Paper›PMID 31105687›Full record

ReviewFrontiers in immunology2019

Non-classical B Cell Memory of Allergic IgE Responses.

Sean P Saunders, Erica G M Ma, Carlos J Aranda, Maria A Curotto de Lafaille

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
3.7field-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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Memory Cells in Atopic Dermatitis: Paving the Way to Disease Modification.International journal of molecular sciences · 2026
    Review
  7. Article
  8. Article
  9. The Mechanisms of Immunoglobulin E Sensitizations in Atopic Dermatitis.Immunology and allergy clinics of North America · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Whence and wherefore IgE?Immunological reviews · 2024
    Review
  17. Article
  18. Review
  19. Article
  20. CD23Science translational medicine · 2024
    Article
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

4 authors at 1 institution in 1 country.

Sean P SaundersDivision of Pulmonary, Critical Care and Sleep Medicine, Laboratory of Allergy and Inflammation, Department of Medicine, New York University, New York, NY, United States.
Erica G M MaDivision of Pulmonary, Critical Care and Sleep Medicine, Laboratory of Allergy and Inflammation, Department of Medicine, New York University, New York, NY, United States.
Carlos J ArandaDivision of Pulmonary, Critical Care and Sleep Medicine, Laboratory of Allergy and Inflammation, Department of Medicine, New York University, New York, NY, United States.
Maria A Curotto de LafailleDivision of Pulmonary, Critical Care and Sleep Medicine, Laboratory of Allergy and Inflammation, Department of Medicine, New York University, New York, NY, United States.
New York University · US

Funding

Cellular and molecular mechanisms of IgE cell memory in allergic responsesR01AI130343 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CUROTTO DE LAFAILLE, MARIA A, LAFAILLE, JUAN · 2017 to 2021
$2.9M
The Origin and Memory of Human IgE ResponsesR21AI133076 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CUROTTO DE LAFAILLE, MARIA A · 2017 to 2018
$466k
NIAID NIH HHS R01 AI130343NIAID NIH HHS R21 AI133076
6 · The paper itself

Abstract

The long-term effectiveness of antibody responses relies on the development of humoral immune memory. Humoral immunity is maintained by long-lived plasma cells that secrete antigen-specific antibodies, and memory B cells that rapidly respond to antigen re-exposure by generating new plasma cells and memory B cells. Developing effective immunological memory is essential for protection against pathogens, and is the basis of successful vaccinations. IgE responses have evolved for protection against helminth parasites infections and against toxins, but IgE is also a potent mediator of allergic diseases. There has been a dramatic increase in the incidence of allergic diseases in recent decades and this has provided the impetus to study the nature of IgE antibody responses. As will be discussed in depth in this review, the IgE memory response has unique features that distinguish it from classical B cell memory.

Indexed as

AnaphylaxisAnimalsGerminal CenterHumansHypersensitivityImmunity, HumoralImmunoglobulin Class SwitchingImmunoglobulin EImmunoglobulin GImmunologic MemoryMiceMice, Inbred BALB CMice, Inbred C57BLPlasma CellsImmunoglobulin EImmunoglobulin GallergyanaphylaxisIgEIgGmemory B cellsplasma cellssequential switching

Identifiers

PMID31105687
PMCPMC6498404
OpenAlexW2940610484

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.