Peanut oral immunotherapy in a pediatric allergy clinic: Patient factors associated with clinical outcomes

被引:5
|
作者
Guarnieri, Katharine M. [1 ,2 ]
Slack, Ian F. [1 ,2 ]
Gadoury-Levesque, Vanessa [3 ]
Eapen, Amy A. [4 ]
Andorf, Sandra [1 ,2 ,5 ]
Lierl, Michelle B. [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Allergy & Immunol, MLC 7028,3333 Burnet Ave, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
[3] McGill Univ, Montreal Childrens Hosp, Dept Pediat, Div Allergy & Clin Immunol, Montreal, PQ, Canada
[4] Henry Ford Hlth Syst, Div Allergy & Clin Immunol, Dept Med, Detroit, MI USA
[5] Cincinnati Childrens Hosp Med Ctr, Div Biomed Informat, Cincinnati, OH 45229 USA
关键词
DOUBLE-BLIND; EFFICACY; CHILDREN; SAFETY;
D O I
10.1016/j.anai.2021.04.003
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Additional information is needed to inform optimal patient selection, expected outcomes, and treatment end points for clinical peanut oral immunotherapy (OIT). Objective: To provide insight into the optimal patient selection, expected outcomes, and treatment end points for clinical peanut oral immunotherapy by analyzing a real-world peanut OIT cohort. Methods: Records were reviewed for 174 children undergoing peanut OIT at a pediatric allergy clinic. Patient age, peanut skin prick test results, and peanut-specific immunoglobulin E (sIgE) results, with inclusion of additional foods in OIT, were analyzed for correlations with OIT outcomes. Results: To date, 144 patients have achieved maintenance dosing, 50 of whom transitioned to ad lib twice weekly peanut ingestion. A total of 30 discontinued OIT. In addition, 47 patients who underwent multifood OIT had no significant difference in reactions (FDR-adjusted P = .48) or time-to-reach maintenance (FDR-adjusted P = .48) compared with those on peanut OIT alone. Age at initiation inversely correlated with achievement of maintenance: 92% of patients 0.5 to less than 5 years, 81% of those 5 to less than 11 years, and 70% of those 11 to less than 18 years reached and continued maintenance (P = .01). Baseline peanut-sIgE level positively correlated with number of reactions during updosing (P < .001) and maintenance (P = .005), though it was not significantly different in patients achieving successful maintenance vs those who discontinued OIT (P = .09). Furthermore, 66% of patients experienced greater than or equal to 1 adverse reaction during OIT. Of those on ad lib peanut ingestion, 2 reported mild reactions after lapses in peanut consumption. Conclusion: Clinical peanut OIT has similar outcomes to research protocols. OIT can be successful in older children and those with high peanut-sIgE levels, though these factors affect outcomes. Clinical and laboratory criteria can guide successful transition to intermittent ad lib peanut consumption. (c) 2021 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:214 / +
页数:13
相关论文
共 50 条
  • [21] Oral immunotherapy for peanut allergy induces eosinophilic esophagitis: three pediatric case reports
    Semancik, Eileen
    Sayej, Wael N.
    PEDIATRIC ALLERGY AND IMMUNOLOGY, 2016, 27 (05) : 539 - 541
  • [22] Clinical and immunological outcomes after randomized trial of baked milk oral immunotherapy for milk allergy
    Dantzer, Jennifer A.
    Lewis, Sloan A.
    Psoter, Kevin J.
    Sutherland, Aaron
    Frazier, April
    Richardson, Eve
    Maiche, Synaida
    Seumois, Gregory
    Peters, Bjoern
    Wood, Robert A.
    JCI INSIGHT, 2025, 10 (01)
  • [23] Early age peanut oral immunotherapy is safe and effective at achieving desensitization in 27 pediatric patients with peanut allergy
    Hemler, Jonathan
    Minnicozzi, Samantha
    Carey, Anne
    Braden, Karen
    Boyd, Kelly
    PEDIATRIC ALLERGY AND IMMUNOLOGY, 2024, 35 (11)
  • [24] Allergen-specific oral immunotherapy for peanut allergy
    Nurmatov, Ulugbek
    Venderbosch, Iris
    Devereux, Graham
    Simons, F. Estelle R.
    Sheikh, Aziz
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2012, (09):
  • [25] Oral Immunotherapy in Food Allergy: A Critical Pediatric Perspective
    Akarsu, Aysegul
    Brindisi, Giulia
    Fiocchi, Alessandro
    Zicari, Anna Maria
    Arasi, Stefania
    FRONTIERS IN PEDIATRICS, 2022, 10
  • [26] Investigation of peanut oral immunotherapy with CpG/peanut nanoparticles in a murine model of peanut allergy
    Srivastava, Kamal D.
    Siefert, Alyssa
    Fahmy, Tarek M.
    Caplan, Michael J.
    Li, Xiu-Min
    Sampson, Hugh A.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 138 (02) : 536 - +
  • [27] Low-dose oral immunotherapy for children with anaphylactic peanut allergy in Japan
    Nagakura, Ken-ichi
    Yanagida, Noriyuki
    Sato, Sakura
    Nishino, Makoto
    Asaumi, Tomoyuki
    Ogura, Kiyotake
    Ebisawa, Motohiro
    PEDIATRIC ALLERGY AND IMMUNOLOGY, 2018, 29 (05) : 512 - 518
  • [28] Oral Immunotherapy for Peanut Allergy: Multipractice Experience With Epinephrine-treated Reactions
    Wasserman, Richard L.
    Factor, Jeffrey M.
    Baker, James W.
    Mansfield, Lyndon E.
    Katz, Yitzhak
    Hague, Angela R.
    Paul, Marianne M.
    Sugerman, Robert W.
    Lee, Jason O.
    Lester, Mitchell R.
    Mendelson, Louis M.
    Nacshon, Liat
    Levy, Michael B.
    Goldberg, Michael R.
    Elizur, Arnon
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2014, 2 (01): : 91 - +
  • [29] Mannosylated Nanoparticles for Oral Immunotherapy in a Murine Model of Peanut Allergy
    Brotons-Canto, Ana
    Gamazo, Carlos
    Martin-Arbella, Nekane
    Abdulkarim, Muthanna
    Gumbleton, Mark
    Quincoces, Gemma
    Penuelas, Ivan
    Irache, Juan M.
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 108 (07) : 2421 - 2429
  • [30] Peanut Allergen Powder-dnfp: A Novel Oral Immunotherapy to Mitigate Peanut Allergy
    Dougherty, John A.
    Wagner, Justin D.
    Stanton, Megan C.
    ANNALS OF PHARMACOTHERAPY, 2021, 55 (03) : 344 - 353