Metabolic Profiling of Immune Responses in Immune-mediated Diseases

Phase

N/A

Condition

Atopic Dermatitis

Primary Immunodeficiency Disorders

Warts

Treatment

N/A

Clinical Study ID

NCT04864886

10000392

000392-I

Ages 18-75
All Genders
Accepts Healthy Volunteers

Study Summary

Background:

The immune system is the part of the body that fights infection. Some people have immune deficiencies that cause skin rashes, make them get sick often with infections, or make it difficult for their skin to heal. Researchers want to learn more to better treat conditions that affect immune response.

Objective:

To learn about how the immune system and skin healing are related to each other.

Eligibility:

People ages 18-75 with primary immune deficiency, eczema, or psoriasis. Healthy volunteers are also needed.

Design:

Participants will be screened with a medical and medicine history and a physical exam. They may take a pregnancy test.

Participants will discuss the medicines or supplements they take as well as skin products they use, such as soaps and lotions.

Participants will have up to 4 skin biopsies taken from the forearm. A needle will inject an anesthetic into the skin where the biopsy will be done. A sharp tool that looks like a tiny cookie cutter will be used to remove a round plug of skin a bit smaller than the tip of a pencil.

Participants will give at least 1 blood sample.

Participants may have optional skin swab collection. A cotton swab will be used to swab the skin on the arm.

Participants may have optional skin tape collection. A sticky strip of tape will be placed on the arm and then removed.

Participants may give leftover samples taken as part of their regular medical care.

Participation will last for about 4 days. Participants will have 2 visits that each last about 1 hour. They may be asked to repeat the study in the future.

Eligibility Criteria

Inclusion

INCLUSION CRITERIA:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

Meets one of the following:
Has documentation of PID confirmed by genetic evaluation demonstrating adeleterious variant in the gene (or genes) known to be associated with immunedeficiency (confirmed PID); or
Has documented variant of undetermined significance in a gene (or genes) thatis predicted to be deleterious in immune function by the investigators OR aclinical history of infections which are more frequent, more chronic, or moresevere than normal (suspected PID); or
Has physician-diagnosed psoriasis; or
Has physician-diagnosed AD; or
Does not have clinically apparent evidence of any monogenic or digenic immunedefect, AD, or psoriasis (healthy volunteers).
Aged 18 to 75 years.
Willing to allow storage of blood, biopsy tissue, bacterial and fungal cultures, andany other samples collected for future research.
Able to provide informed consent.

Exclusion

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

Current or prior (within 3 months) anticoagulant or anti-platelet therapy (otherthan aspirin or non-steroidal anti-inflammatory drugs).
Current or prior (within 3 months) use of immunomodulatory drugs (eg, chemotherapy,steroids), except if approved by the principal investigator.
History of keloid formation.
Pregnancy, lactating, or breastfeeding.
Any condition that, in the opinion of the investigator, contraindicatesparticipation in the study.

Co-enrollment guidelines: Participants may be co-enrolled in other studies; however, study staff should be notified of co-enrollment.

Study Design

August 10, 2021

June 30, 2027

Study Description

Study Description:

This is an exploratory sample collection study enrolling adult healthy volunteers and patients with immune-mediated diseases to elucidate the metabolic signatures associated with immune-mediated diseases. We hypothesize that activation of, and responses to, specific immune pathways will require metabolic changes within cells, serum, and skin.

Following screening and baseline procedures, including blood draw, participants who are able to attend onsite visits will undergo skin biopsies. The skin biopsies will involve up to 4 biopsies: 2 initial punch biopsies 2 mm in diameter, optionally followed by 1 or 2 punch biopsies 3 (+/-10) days later using a 3-mm punch to encompass the initial biopsy site(s), capturing the tissue at 3-14 days of healing. There will be an option for blister induction to maximize keratinocyte collection. Blister induction involves creating 8 blisters on the forearm and removing the tops of the blisters for primary cell culture derivation. In addition, skin swabs and tape strips may be collected to assess for microbial or host markers of epithelial repair. Peripheral blood and functional signatures will be collected with the initial and follow-up biopsies to compare metabolic and functional signatures in peripheral blood cells and serum with those in the skin. Urine may be collected in order to detect metabolites that are not as easily detected in the blood. After day 0 (or 3-14, if the participant has that optional visit), participation in the study will be complete. At-home participants who cannot attend onsite visits may enroll for survey

data collection and optional at-home sample collection (with at least one sample type required). Exposome data will be collected to assess how environmental, occupational, and dietary exposures associate with the results.

Samples and data will be stored for future research use.

Objectives:

Primary Objectives:

Evaluate metabolic profiles in immune activation associated with known or suspected immune-mediated disorders.
Determine whether there are abnormalities in specific tissue repair pathways, such as epithelial to mesenchymal transition (EMT), that are associated with immune-mediated disorders.

Secondary Objectives:

Not applicable.

Exploratory Objective:

Evaluate how metabolic profiles in immune activation vary with differing occupational, environmental, and/or dietary exposures.

Endpoints:

Primary Endpoints:

Fold differences in metabolic pathways associated with immune pathways.
Fold differences in metabolic pathways related to wound healing.
Change in relative abundance of microbial skin taxa and/or skin metabolites associated with wound healing or immune-mediated disorders.

Secondary Endpoints: