Food allergic reactions are an increasing cause of morbidity and mortality worldwide, and are triggered by allergen-specific IgE antibodies bound to mast cell and basophil effector cells. The molecular features that make some human IgE antibodies pathogenic have been difficult to study from polyclonal sera that contain mixtures of unknown numbers and proportions of antibody types. Similarly, the mechanisms by which IgG4 and IgG1 antibodies elicited by oral immunotherapy (OIT) can protect patients from allergic reactions would be clarified by studying defined antibodies of known sequence from patients following treatment. We will study the functional activity of defined peanut allergen-specific human IgE, IgG4 and IgG1 monoclonal antibodies (mAbs) isolated from symptomatic allergic patients compared to sensitized but non-allergic controls, and from patients post-treatment who vary in their response to OIT. Cultured primary human mast cells will be used as effector cells, and will be studied with three assays extending from early cell activation (Calcium influx), through effector release, to later cytokine secretion. IgE clones will be evaluated for their allergen specificity, binding affinity, and epitope recognition, and tested in combinations to determine which species can sensitize mast cells. Blocking of mast cell activation by mAb IgG4 and IgG1 will be tested, and Fc mutations used to determine whether Fc? receptors contribute to decreases in mast cell effector functions. Finally, IgE and other antibody isotypes isolated from patient gastrointestinal tract biopsies will be compared to antibodies isolated from the blood, to determine whether there is enrichment for potentially pathogenic IgE in the mucosal sites where allergic reactions occur. These studies are likely to have a significant impact on basic and translational human allergy research, as they will use a fully human, but well-defined experimental system to identify the molecular features of pathogenic IgE clones in the blood and GI tracts of allergic patients, and evaluate potential IgG4 and IgG1- mediated mechanisms of protection following OIT. Improved understanding of IgE clone affinities, epitope reactivities, and combinations that result in mast cell sensitization could enable better diagnostic and prognostic testing in allergic patients, while more knowledge about the criteria leading to protective IgG4 and IgG1 could guide therapeutic trials and the development of improved immunotherapy regimens.

Public Health Relevance

This project will isolate individual human antibodies specific for peanut allergens from patients, and use them to make human mast cells (one of the main cell types responsible for allergic reactions) sensitized to peanut. Other types of antibodies that may protect against allergic reactions will also be isolated and tested for their effect on the mast cells. Studying allergic reactions triggered by peanut in this well-defined system should identify the kinds of antibodies that lead to clinical peanut allergy, enable better prediction of which patients may have severe reactions, and help prioritize strategies for improving therapies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI125567-03
Application #
9623318
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Davidson, Wendy F
Project Start
2017-02-15
Project End
2022-01-31
Budget Start
2019-02-01
Budget End
2020-01-31
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Stanford University
Department
Pathology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94304
Boyd, Scott Dexter; Hoh, Ramona Amy; Nadeau, Kari Christine et al. (2017) Immune monitoring for precision medicine in allergy and asthma. Curr Opin Immunol 48:82-91