Blood Samples for the Study of Peanut, Tree Nut and Other Food Allergies

University of Colorado Denver (CU Denver)

Status: Enrolling

Conditions: Other Food Allergies; Tree Nut Allergies; Peanut Allergies

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT02192866

13-2102

UL1TR001082 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Food allergies are now a major problem. These experiments involve getting blood from people with food allergies and from people without food allergies. The blood collected will be used to answer questions and find information about peanut and other food allergies.

Samples will come from:

• People signed up by the investigators at the University of Colorado Denver
• University of North Carolina, Massachusetts General Hospital, Children's Hospital of Colorado and the Immune Tolerance Network (Benaroya Research Institute) where people have been treated for peanut allergies
• University of North Carolina, Massachusetts General Hospital, National Jewish Health and The Children's Hospital in Denver where people have taken part or will take part in clinically indicated oral food challenges.

Blood and health histories from the University of North Carolina, Massachusetts General Hospital, National Jewish Health, The Children's Hospital and the Immune Tolerance Network will not have personal information linked.

The specific aims of this experiment are:

1. Come up with a lab test that will predict how bad an allergic reaction will be to peanuts.
2. Find out what part of a peanut causes allergic reactions.
3. Come up with preventions that can block peanut allergies.
4. Find the strongest proteins in walnuts.

Full description

Overview: This is a protocol for obtaining serum, plasma, and cells from subjects with specific food allergies and from controls to be used in studies of peanut and other allergens. We are only asking the CTRC for help with drawing blood, separating serum, labeling tubes and to aliquot the serum. In addition, we will receive de-identified serum and plasma from other institutions and de-identified cord blood from the University of Colorado Denver Cord Blood bank.

The previous version of this application was COMIRB protocol 09-0813. This was last updated 03-03-2016. Much of the work outlined in protocol 09-0813 was completed and a manuscript is under review. This protocol is still only for the purpose of drawing blood and obtaining clinical histories. As such the risks and benefits in the informed consent have not changed.

Based on new NIH funding (RO3 AI 164349; started 7-09-21) and RO1-AI165866 (9th %-tile; scheduled to begin 09-01-21), the project now includes 5 specific aims (Aims #1-5). Aims 1 & 2 are part of an R21 funded project (R21 AI135397; 11/16/2018-10/31/2020; extended until 10/31/2021 without additional funds) to Dr. Dreskin. Aims 3 & 4 are part of an R21 funded project (R21 AI137881; 11/28/2018-10/31/2020; extended until 10/31/2021 without additional funds) to Dr. Chen (Dr. Dreskin is Co-PI). These proposals are highly complementary and each only needs access to blood samples. Dr. Dreskin's proposal consists of in vitro experiments to test IgE binding to novel peptides. Dr. Chen's proposal uses human serum or plasma as a source of IgE with which to identify and characterize mimotopes for murine studies. Aim 5 is an exploratory aim to obtain preliminary data for an RO1 to be submitted in 2019. For all of these projects, the only experiments that involve human materials are ex vivo assays of basophil activation, in vitro assays of IgE binding and generation of humanized mice using de-identified cord blood that will otherwise be discarded. There are no therapeutic interventions for human subjects.

Enrollment: 270 estimated patients

Sex: All

Ages: 1 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

This protocol is to draw blood for a variety of related studies of food allergy. For this reason, we will list each group of subjects and the inclusion criteria for that group.

1. De-identified sera or plasma from patients who have undergone Oral ImmunoTherapy (OIT) for peanut allergy. These samples already exist.

   • Inclusion criteria:

     1. patients have been enrolled in a controlled trial of OIT for peanuts, and had at least one oral challenge.
     2. Age 1-75.

2. De-identified samples from patients who are undergoing clinically indicated food challenges for peanut allergy.

   • Inclusion criteria:

     1. concern regarding possible allergy to peanuts,
     2. age 1-75,
     3. plan to undergo a clinically indicated challenge with peanuts.

3. Patients with peanut allergy.

   • Inclusion criteria:

     1. excellent history of a systemic reaction to peanuts,
     2. age 6-75.

4. Patients with other food allergies (especially tree nuts).

   • Inclusion criteria:

     1. excellent history of a systemic reaction to tree nuts or other foods,
     2. age 6-75.

5. Normal controls.

   • Inclusion criteria:

     1. no known food allergies,
     2. recent ingestion of peanuts without difficulty, and
     3. age 6-75.

Exclusion criteria

1. Any known significant medical or psychiatric diagnosis
2. Use of an investigational drug within 30 days
3. Use of omalizumab (anti-IgE; Xolair) within 6 months

Trial design

270 participants in 3 patient groups

Peanut allergic

Description:

No intervention(s) to be administered.

Other food allergic

Description:

No intervention(s) to be administered.

Controls

Description:

No intervention(s) to be administered.