HIP: Human Immunome Program

Sponsor
Vanderbilt University Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT03118687
Collaborator
Human Vaccines Project (Other)
2
1
35.6
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Study Details

Study Description

Brief Summary

The Human Immunome Program is a large-scale, open-source effort seeking to fill a major gap in our knowledge of the immune system. The power of the immune system to fight disease lies in its ability recognize and adapt to an astonishing range of threats from viruses, parasites and bacteria to cancer cells. Underlying this ability is a vast but specific set of genes and molecular structures known as the human immunome, or the "parts list" of the immune system. This study aims to decipher the genetic sequences that make up this part list and link it to information about a person's microbiome composition and characteristics such as health history, race, and demographics over time. This information, made freely available to the public for use in research in de-identified form, will allow investigators to answer a wide variety of different questions about immune system function. This could transform how we diagnose, prevent and treat disease though the identification of new biomarkers while enabling highly targeted, computationally designed vaccines and therapies that reduce time and risk of product development.

Condition or Disease Intervention/Treatment Phase
  • Other: Biospecimen and survey collection

Study Design

Study Type:
Observational
Actual Enrollment :
2 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Human Immunome Program
Actual Study Start Date :
Jul 1, 2017
Actual Primary Completion Date :
Jun 18, 2020
Actual Study Completion Date :
Jun 18, 2020

Outcome Measures

Primary Outcome Measures

  1. The entire expressed B and T cell receptor repertoire ("Immunome") of the human immune system [10 years]

    The B and T cell receptor repertoire will be sequenced. The sequencing will continue until no new unique sequences appear.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 49 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy male and female volunteers between the ages of 18 - 49 years of age at the time of first enrollment.

  • Ability to comply: Participant willing and able to comply with the requirements of the protocol.

  • Consent: Participants who have given informed consent for participation in the study

Exclusion Criteria:
Reason for exclusion throughout the entire study period:
  • History of severe anemia requiring blood transfusion or current Hemoglobin < 10g/dL.

  • Currently pregnant or pregnancy within 6 months.

  • Current participation in another study resulting in blood collection which exceeds 550 ml in an 8 week period or occurs more frequently than 2 times per week.

  • Temperature >101.4F

  • Any condition which, in the opinion of the investigator, might interfere with study objectives.

  • Any reason which, in the opinion of the investigator, adds additional risk to the patient.

Reason for exclusion in year 0 but not in year 1-9:
  • History of known HIV infection or treatment.

  • Immunosuppressive disease or use of systemic immunosuppressive therapy using drugs or cytotoxic agents including prednisone (IV, oral or inhaled) less than 6 months ago.

  • History of diabetes mellitus -or a glucose (on CMP) ≥200 mg/dL.

  • History of cancer including skin cancer.

  • History of autoimmune disorders including but not limited to: Ulcerative colitis, Crohn's, Inflammatory Bowel Disease, Rheumatoid Arthritis, Scleroderma, Systemic lupus Erythematosus, Mixed Connective Tissue Disease, Graves, Autoimmune Thyroiditis, Hashimoto's Thyroiditis, Psoriasis, Multiple Sclerosis, Guillain-Barre Syndrome, Chronic Inflammatory demyelinating polyneuropathy, Myasthenia Gravis, Vasculitis, Alopecia areata, autoimmune hemolytic anemia, autoimmune hepatitis, dermatomyositis, idiopathic thrombocytopenic purpura, pemphigus, pernicious anemia, polyarteritis nodosa, polymyositis, Sjogren's Syndrome, Wegener's

  • Severe obesity = (BMI >40 kg/m2).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vanderbilt University Medical Center Nashville Tennessee United States 37232

Sponsors and Collaborators

  • Vanderbilt University Medical Center
  • Human Vaccines Project

Investigators

  • Principal Investigator: James E Crowe Jr., M.D., Vanderbilt University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
James E. Crowe, Jr., Principal Investigator, Vanderbilt University Medical Center
ClinicalTrials.gov Identifier:
NCT03118687
Other Study ID Numbers:
  • IRB#170398
First Posted:
Apr 18, 2017
Last Update Posted:
Feb 8, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by James E. Crowe, Jr., Principal Investigator, Vanderbilt University Medical Center

Study Results

No Results Posted as of Feb 8, 2021