Gastrointestinal Eosinophil Responses in a Longitudinal, Randomized Trial of Peanut Oral Immunotherapy

被引:45
作者
Wright, Benjamin L. [1 ,2 ]
Fernandez-Becker, Nielsen Q. [3 ]
Kambham, Neeraja [3 ,4 ]
Purington, Natasha [3 ]
Cao, Shu [3 ]
Tupa, Dana [3 ]
Zhang, Wenming [3 ]
Sindher, Sayantani B. [3 ]
Rank, Matthew A. [1 ,2 ]
Kita, Hirohito [1 ,5 ]
Katzka, David A. [6 ]
Shim, Kelly P. [1 ,2 ]
Bunning, Bryan J. [3 ]
Doyle, Alfred D. [1 ]
Jacobsen, Elizabeth A. [1 ,5 ]
Tsai, Mindy [3 ,4 ]
Boyd, Scott D. [4 ]
Manohar, Monali [3 ]
Chinthrajah, R. Sharon [3 ]
机构
[1] Mayo Clin Arizona, Dept Med, Div Allergy Asthma & Clin Immunol, Scottsdale, AZ USA
[2] Phoenix Childrens Hosp, Div Pulmonol, Phoenix, AZ USA
[3] Stanford Univ, Sch Med, Sean N Parker Ctr Allergy & Asthma Res, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[5] Dept Immunol, Mayo Clin Arizona, Scottsdale, AZ USA
[6] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
关键词
EREFS; EoEHSS; Inflammation; Food Allergy; DILATED INTERCELLULAR SPACES; REFLUX DISEASE; FOOD ALLERGY; ESOPHAGITIS; DIAGNOSIS; FEATURES; CELLS;
D O I
10.1016/j.cgh.2020.05.019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Gastrointestinal side effects are common during oral immunotherapy (OIT) and eosinophilic esophagitis (EoE) is a potential complication. We aimed to characterize eosinophilic gastrointestinal responses to peanut OIT, in which peanut protein is given orally, with incremental increases in dose over time. METHODS: Twenty adults with IgE-mediated peanut allergy were randomly assigned to groups given peanut OIT (n = 15) or placebo (n = 5); 1 additional subject withdrew before randomization. Serial gastrointestinal biopsies were collected at baseline (n = 21, 0 weeks), following dose escalation (n = 10, 52 weeks), and during the maintenance phase (n = 11, 104 weeks). Endoscopic findings were characterized using the EoE endoscopic reference score. Biopsies were assessed for eosinophils per high-power field (eos/hpf) and other pathology features using EoE histologic scoring system scores. We performed immunohistochemical analyses of eosinophil peroxidase deposition, quantified using automated image analysis. RESULTS: At baseline, no subjects reported current gastrointestinal symptoms. However, 3 of the 21 subjects (14%) had esophageal peak eosinophil counts 15 eos/hpf and all subjects had dilated intercellular spaces (DIS). OIT induced or exacerbated esophageal eosinophilia (EE) at 52 weeks in most subjects (peak eosinophil counts >5 eos/hpf in 6 of 7 patients [86%]; peak eosinophil counts > 15 eos/hpf in 4 of 7 patients [57%]). One subject met clinicopathologic criteria for EoE and withdrew; no significant changes in esophageal peak eosinophil counts were observed in the placebo group. EE in the OIT group corresponded with significant increases in EoE histologic scoring system scores and deposition of eosinophil peroxidase. In 4 of 6 participants (67%), OIT-induced EE and gastrointestinal eosinophilia resolved by the end of the maintenance phase. Gastrointestinal symptoms were not clearly associated with EE or gastrointestinal eosinophilia. CONCLUSIONS: In this pilot study, we found that peanut OIT-induced EE and gastrointestinal eosinophilia are usually transient and are not always associated with gastrointestinal symptoms.
引用
收藏
页码:1151 / +
页数:23
相关论文
共 43 条
[1]   Assessing the efficacy of oral immunotherapy for the desensitisation of peanut allergy in children (STOP II): a phase 2 randomised controlled trial [J].
Anagnostou, Katherine ;
Islam, Sabita ;
King, Yvonne ;
Foley, Loraine ;
Pasea, Laura ;
Bond, Simon ;
Palmer, Chris ;
Deighton, John ;
Ewan, Pamela ;
Clark, Andrew .
LANCET, 2014, 383 (9925) :1297-1304
[2]   Anti-IgE treatment with oral immunotherapy in multifood allergic participants: a double-blind, randomised, controlled trial [J].
Andorf, Sandra ;
Purington, Natasha ;
Block, Whitney M. ;
Long, Andrew J. ;
Tupa, Dana ;
Brittain, Erica ;
Spergel, Amanda Rudman ;
Desai, Manisha ;
Galli, Stephen J. ;
Nadeau, Kari C. ;
Chinthrajah, R. Sharon .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2018, 3 (02) :85-94
[3]   Oesophageal eosinophilia in children with coeliac disease [J].
Ari, Anne ;
Morgenstern, Sara ;
Chodick, Gabriel ;
Matar, Manar ;
Silbermintz, Ari ;
Assa, Amit ;
Mozer-Glassberg, Yael ;
Rinawi, Firas ;
Nachmias-Friedler, Vered ;
Shamir, Raanan ;
Zevit, Noam .
ARCHIVES OF DISEASE IN CHILDHOOD, 2017, 102 (09) :825-829
[4]   Treatment for food allergy [J].
Burks, A. Wesley ;
Sampson, Hugh A. ;
Plaut, Marshall ;
Lack, Gideon ;
Akdis, Cezmi A. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 141 (01) :1-9
[5]   Histologic eosinophilic gastritis is a systemic disorder associated with blood and extragastric eosinophilia, TH2 immunity, and a unique gastric transcriptome [J].
Caldwell, Julie M. ;
Collins, Margaret H. ;
Stucke, Emily M. ;
Putnam, Philip E. ;
Franciosi, James P. ;
Kushner, Jonathan P. ;
Abonia, J. Pablo ;
Rothenberg, Marc E. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2014, 134 (05) :1114-1124
[6]   Dilated intercellular spaces of esophageal epithelium in nonerosive reflux disease patients with physiological esophageal acid exposure [J].
Caviglia, R ;
Ribolsi, M ;
Maggiano, N ;
Gabbrielli, AM ;
Emerenziani, S ;
Guarino, MPL ;
Carotti, S ;
Habib, FI ;
Rabitti, C ;
Cicala, M .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (03) :543-548
[7]   IgE-activated basophils regulate eosinophil tissue entry by modulating endothelial function [J].
Cheng, Laurence E. ;
Sullivan, Brandon M. ;
Retana, Lizett E. ;
Allen, Christopher D. C. ;
Liang, Hong-Erh ;
Locksley, Richard M. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2015, 212 (04) :513-524
[8]   Sustained outcomes in oral immunotherapy for peanut allergy (POISED study): a large, randomised, double-blind, placebo-controlled, phase 2 study [J].
Chinthrajah, R. Sharon ;
Purington, Natasha ;
Andorf, Sandra ;
Long, Andrew ;
O'Laughlin, Katherine L. ;
Lyu, Shu Chen ;
Manohar, Monali ;
Boyd, Scott D. ;
Tibshirani, Robert ;
Maecker, Holden ;
Plaut, Marshall ;
Mukai, Kaori ;
Tsai, Mindy ;
Desai, Manisha ;
Galli, Stephen J. ;
Nadeau, Kari C. .
LANCET, 2019, 394 (10207) :1437-1449
[9]   Oral immunotherapy for peanut allergy (PACE): a systematic review and meta-analysis of efficacy and safety [J].
Chu, Derek K. ;
Wood, Robert A. ;
French, Shannon ;
Fiocchi, Alessandro ;
Jordana, Manel ;
Waserman, Susan ;
Brozek, Jan L. ;
Schuenemann, Holger J. .
LANCET, 2019, 393 (10187) :2222-2232
[10]   Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo [J].
Chu, Derek K. ;
Jimenez-Saiz, Rodrigo ;
Verschoor, Christopher P. ;
Walker, Tina D. ;
Goncharova, Susanna ;
Llop-Guevara, Alba ;
Shen, Pamela ;
Gordon, Melissa E. ;
Barra, Nicole G. ;
Bassett, Jennifer D. ;
Kong, Joshua ;
Fattouh, Ramzi ;
McCoy, Kathy D. ;
Bowdish, Dawn M. ;
Erjefalt, Jonas S. ;
Pabst, Oliver ;
Humbles, Alison A. ;
Kolbeck, Roland ;
Waserman, Susan ;
Jordana, Manel .
JOURNAL OF EXPERIMENTAL MEDICINE, 2014, 211 (08) :1657-1672