Evidence map›Paper›PMID 27609658›Full record

Trial reportThe Journal of allergy and clinical immunology2017

Omalizumab facilitates rapid oral desensitization for peanut allergy.

Andrew J MacGinnitie, Rima Rachid, Hana Gragg, Sara V Little, Paul Lakin, Antonella Cianferoni, Jennifer Heimall, Melanie Makhija, Rachel Robison, R Sharon Chinthrajah and 14 more

Abstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 132 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed, 6 pooled it
21.4field-weighted citation impact, top 1% 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

132 citing papers in PubMed, 6 syntheses or guidelines pooled it, 317 citations in OpenAlex.

  1. Pooled it
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  6. Pooled it
  7. Trial
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  9. Omalizumab for the Treatment of Multiple Food Allergies.The New England journal of medicine · 2024
    Trial
  10. Trial
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  12. Immunoglobulin E blockade during food allergen ingestion enhances the induction of inhibitory immunoglobulin G antibodies.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2019
    Trial
  13. Trial
  14. Eosinophilic esophagitis during peanut oral immunotherapy with omalizumab.The journal of allergy and clinical immunology. In practice
    Trial
  15. Review
  16. Update on biologic and small molecules treatments in pediatric allergic diseases.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Review
  17. Article
  18. Article
  19. Review
  20. Article

72 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 4 institutions in 1 country.

Andrew J MacGinnitieDivision of Immunology, Boston Children's Hospital, Boston, Mass.
Rima RachidDivision of Immunology, Boston Children's Hospital, Boston, Mass.
Hana GraggClinical Research Center, Boston Children's Hospital, Boston, Mass.
Sara V LittleDivision of Immunology, Boston Children's Hospital, Boston, Mass.
Paul LakinClinical Research Center, Boston Children's Hospital, Boston, Mass.
Antonella CianferoniDivision of Allergy, Children's Hospital of Philadelphia, Philadelphia, Pa.
Jennifer HeimallDivision of Allergy, Children's Hospital of Philadelphia, Philadelphia, Pa.
Melanie MakhijaAllergy Division, the Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill.
Rachel RobisonAllergy Division, the Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill.
R Sharon ChinthrajahDivision of Allergy, Immunology, and Rheumatology, Lucille Packard Children's Hospital, Palo Alto, Calif.
John LeeDivision of Immunology, Boston Children's Hospital, Boston, Mass.
Jennifer LebovidgeDivision of Immunology, Boston Children's Hospital, Boston, Mass.
Tina DominguezDivision of Allergy, Immunology, and Rheumatology, Lucille Packard Children's Hospital, Palo Alto, Calif.
Courtney RooneyDivision of Allergy, Children's Hospital of Philadelphia, Philadelphia, Pa.
Megan Ott LewisDivision of Allergy, Children's Hospital of Philadelphia, Philadelphia, Pa.
Jennifer KossAllergy Division, the Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill.
Elizabeth Burke-RobertsDivision of Immunology, Boston Children's Hospital, Boston, Mass.
Kimberly ChinClinical Research Center, Boston Children's Hospital, Boston, Mass.
Tanya LogvinenkoClinical Research Center, Boston Children's Hospital, Boston, Mass.
Jacqueline A PongracicAllergy Division, the Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill.
Dale T UmetsuGenentech, South San Francisco, Calif.
Jonathan SpergelDivision of Allergy, Children's Hospital of Philadelphia, Philadelphia, Pa.
Kari C NadeauDivision of Allergy, Immunology, and Rheumatology, Lucille Packard Children's Hospital, Palo Alto, Calif.
Lynda C SchneiderDivision of Immunology, Boston Children's Hospital, Boston, Mass. Electronic address: Lynda.Schneider@childrens.harvard.edu.
Boston Children's Hospital · USChildren's Hospital of Philadelphia · USLurie Children's Hospital · USLucile Packard Children's Hospital · US

Funding

Harvard Clinical and Translational Science CenterUL1TR001102 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2013 to 2017
$106.2M
INSTITUTIONAL CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR024134 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$70.4M
Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
Tracking allergen specific T cells in multi-food allergyU19AI104209 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 2013 to 2025
$17.3M
SEAL (Stopping Atopic dermatitis and ALlergy) Study: Prevent allergy by enhancing the skin barrierU01AI147462 · NIAID · STANFORD UNIVERSITY · PI Mary Johnson, GIDEON LACK · 2020 to 2026
$14.0M
Multidisciplinary Clinical and Translational Science (MCTS) Program (UL1)UL1TR000150 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LLOYD-JONES, DONALD M · 2012 to 2013
$10.1M
NCATS NIH HHS UL1 TR000003NCATS NIH HHS UL1 TR000150NCATS NIH HHS UL1 TR001102NCATS NIH HHS UL1 TR001422NCRR NIH HHS UL1 RR024134NIAID NIH HHS U01 AI147462NIAID NIH HHS U19 AI104209
6 · The paper itself

Abstract

backgroundPeanut oral immunotherapy is a promising approach to peanut allergy, but reactions are frequent, and some patients cannot be desensitized. The anti-IgE medication omalizumab (Xolair; Genentech, South San Francisco, Calif) might allow more rapid peanut updosing and decrease reactions.

objectiveWe sought to evaluate whether omalizumab facilitated rapid peanut desensitization in highly allergic patients.

methodsThirty-seven subjects were randomized to omalizumab (n = 29) or placebo (n = 8). After 12 weeks of treatment, subjects underwent a rapid 1-day desensitization of up to 250 mg of peanut protein, followed by weekly increases up to 2000 mg. Omalizumab was then discontinued, and subjects continued on 2000 mg of peanut protein. Subjects underwent an open challenge to 4000 mg of peanut protein 12 weeks after stopping study drug. If tolerated, subjects continued on 4000 mg of peanut protein daily.

resultsThe median peanut dose tolerated on the initial desensitization day was 250 mg for omalizumab-treated subjects versus 22.5 mg for placebo-treated subject. Subsequently, 23 (79%) of 29 subjects randomized to omalizumab tolerated 2000 mg of peanut protein 6 weeks after stopping omalizumab versus 1 (12%) of 8 receiving placebo (P < .01). Twenty-three subjects receiving omalizumab versus 1 subject receiving placebo passed the 4000-mg food challenge. Overall reaction rates were not significantly lower in omalizumab-treated versus placebo-treated subjects (odds ratio, 0.57; P = .15), although omalizumab-treated subjects were exposed to much higher peanut doses.

conclusionOmalizumab allows subjects with peanut allergy to be rapidly desensitized over as little as 8 weeks of peanut oral immunotherapy. In the majority of subjects, this desensitization is sustained after omalizumab is discontinued. Additional studies will help clarify which patients would benefit most from this approach.

Indexed as

Desensitization, ImmunologicAdolescentAdultAllergensAnti-Allergic AgentsArachisChildDouble-Blind MethodFemaleHumansImmunoglobulin EMaleOmalizumabPeanut HypersensitivitySkin TestsYoung AdultAllergensAnti-Allergic AgentsImmunoglobulin EOmalizumabdesensitizationfood allergyomalizumabPeanut allergy

Identifiers

PMID27609658
PMCPMC5369605
OpenAlexW2284588816

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.