Peanut-Specific IgG4 and IgA in Saliva Are Modulated by Peanut Oral Immunotherapy

被引:10
|
作者
Smeekens, Johanna M. [1 ,2 ]
Baloh, Carolyn [3 ]
Lim, Noha [3 ]
Larson, David [3 ]
Qin, Tielin [3 ]
Wheatley, Lisa [4 ]
Kim, Edwin H. [1 ,2 ]
Jones, Stacie M. [5 ,6 ]
Burks, A. Wesley [1 ,2 ]
Kulis, Michael D. [1 ,2 ]
机构
[1] UNC Sch Med, Div Allergy & Immunol, Dept Pediat, Chapel Hill, NC USA
[2] UNC Sch Med, Dept Pediat, UNC Food Allergy Initiat, Chapel Hill, NC USA
[3] Immune Tolerance Network, Bethesda, MD USA
[4] Nat Inst Allergy & Infect Dis NIAID, Natl Inst Hlth, Bethesda, MD USA
[5] Univ Arkansas Med Sci, Dept Pediat, Little Rock, AR USA
[6] Arkansas Childrens Hosp, Little Rock, AR USA
基金
美国国家卫生研究院;
关键词
Peanut allergy; Oral immunotherapy; IgA; IgG4; Saliva; IMMUNE-RESPONSES; CHILDREN; ANTIBODIES; TRIAL;
D O I
10.1016/j.jaip.2022.07.030
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Antigen-specific immunoglobulin responses have yet to be studied at the oral mucosal surface during peanut oral immunotherapy (PnOIT). OBJECTIVE: We aimed to quantify salivary peanut-specific IgG4 (PNsIgG4) and IgA (PNsIgA) and total IgG4 and IgA in participants from the Immune Tolerance Network's IMPACT study, a phase 2 PnOIT trial. METHODS: Peanut-allergic children, aged 12 months to younger than 48 months at screening, were enrolled and randomized to PnOIT or placebo oral immunotherapy (OIT) for 134 weeks. Per-protocol analysis included 69 PnOIT and 23 placebo participants. Double-blind, placebo-controlled food challenges were conducted at weeks 134 and 160 to assess desensitization and remission, respectively. Saliva samples were collected at baseline and 30, 82, 134, and 160 weeks to quantify PNsIgG4, PNsIgA, and total IgG4 and IgA. RESULTS: Participants who received PnOIT experienced significant increases in PNsIgG4 in saliva, whereas participants on placebo did not (P <.01 at all time points). The PNsIgA/total IgA ratio was also significantly increased in participants treated with PnOIT when compared with those receiving placebo at 30 and 82 weeks (P <.05). During PnOIT, desensitized participants had increased PNsIgA that plateaued, whereas the not desensitized/no remission group did not change over time. Interestingly, when the PnOIT group was evaluated by clinical outcome, PNsIgA was higher at baseline in the not desensitized/no remission group than in the desensitized/remission group (P <.05). CONCLUSIONS: PnOIT induces substantial increases in allergen-specific IgG4 and IgA in saliva. These data provide insight into OIT-induced mucosal responses and suggest the utility of these easily obtained samples for biomarker development. (c) 2022 American Academy of Allergy, Asthma & Immunology
引用
收藏
页码:3270 / 3275
页数:6
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