Evidence map›Paper›PMID 20458139›Full record

ArticleThe Journal of clinical investigation2010

Antibodies specific for a segment of human membrane IgE deplete IgE-producing B cells in humanized mice.

Hans D Brightbill, Surinder Jeet, Zhonghua Lin, Donghong Yan, Meijuan Zhou, Martha Tan, Allen Nguyen, Sherry Yeh, Donnie Delarosa, Steven R Leong and 17 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05042830 (Contribution of Local Nasal IgE Production to the Boost of Systemic Allergen-specific IgE Production Upon Nasal Allergen Contact - an Explorative Pilot Study), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.6field-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.

NCT05042830 narecruitingnot on this mapstarted 2021, after this paper: background citation

Contribution of Local Nasal IgE Production to the Boost of Systemic Allergen-specific IgE Production Upon Nasal Allergen Contact - an Explorative Pilot Study

TypeinterventionalSponsorMedical University of ViennaRan2021 to 2026Enrolled30ConditionsAllergyArmsBlood sampling, Nasal biopsies, Nasal specimen collection, Mucosal RNA sampling, Intranasal challenge
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 109 citations in OpenAlex.

  1. Trial
  2. T cell engagers in autoimmune diseases.Nature reviews. Immunology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. B cell receptor ligation induces IgE plasma cell elimination.The Journal of experimental medicine · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. The use of biologics for immune modulation in allergic disease.The Journal of clinical investigation · 2019
    Review
  15. Article
  16. Article
  17. Review
  18. Potential Pitfalls of the Humanized Mice in Modeling Sepsis.International journal of inflammation · 2018
    Review
  19. Review
  20. 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

27 authors at 1 institution in 1 country.

Hans D BrightbillDepartment of Immunology, Genentech Inc., South San Francisco, California 94080, USA.
Surinder Jeet
Zhonghua Lin
Donghong Yan
Meijuan Zhou
Martha Tan
Allen Nguyen
Sherry Yeh
Donnie Delarosa
Steven R Leong
Terence Wong
Yvonne Chen
Mark Ultsch
Elizabeth Luis
Sree Ranjani Ramani
Janet Jackman
Lino Gonzalez
Mark S Dennis
Anan Chuntharapai
Laura DeForge
Y Gloria Meng
Min Xu
Charles Eigenbrot
Wyne P Lee
Canio J Refino
Mercedesz Balazs
Lawren C Wu
Institute of Automation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgE-mediated hypersensitivity is central to the pathogenesis of asthma and other allergic diseases. Although neutralization of serum IgE with IgE-specific antibodies is in general an efficacious treatment for allergic asthma, one limitation of this approach is its lack of effect on IgE production. Here, we have developed a strategy to disrupt IgE production by generating monoclonal antibodies that target a segment of membrane IgE on human IgE-switched B cells that is not present in serum IgE. This segment is known as the M1' domain, and using genetically modified mice that contain the human M1' domain inserted into the mouse IgE locus, we demonstrated that M1'-specific antibodies reduced serum IgE and IgE-producing plasma cells in vivo, without affecting other immunoglobulin isotypes. M1'-specific antibodies were effective when delivered prophylactically and therapeutically in mouse models of immunization, allergic asthma, and Nippostrongylus brasiliensis infection, likely by inducing apoptosis of IgE-producing B cells. In addition, we generated a humanized M1'-specific antibody that was active on primary human cells in vivo, as determined by its reduction of serum IgE levels and IgE plasma cell numbers in a human PBMC-SCID mouse model. Thus, targeting of human IgE-producing B cells with apoptosis-inducing M1'-specific antibodies may be a novel treatment for asthma and allergy.

Indexed as

AnimalsAntibodiesAntibodies, MonoclonalAsthmaB-LymphocytesHumansHypersensitivityHypersensitivity, ImmediateImmunizationMiceMice, SCIDMice, TransgenicNippostrongylusAntibodiesAntibodies, Monoclonal

Identifiers

PMID20458139
PMCPMC2877936
OpenAlexW2044914234

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.