The 10,000 Immunomes Project: Building a Resource for Human Immunology.

Cell Rep

Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, CA 94158, USA; Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94158, USA. Electronic address:

Published: October 2018

AI Article Synopsis

  • The immune system is increasingly recognized for its roles beyond infection and inflammation, impacting areas like cancer, metabolism, and neurobiology.
  • The 10,000 Immunomes Project (10KIP) aims to create a diverse reference for human immunology using data from the ImmPort database.
  • The project explores variations in immune responses based on factors such as age, race, and sex, and provides valuable data for further research in immunology, including insights into pregnancy-related changes.

Article Abstract

There is increasing appreciation that the immune system plays critical roles not only in the traditional domains of infection and inflammation but also in many areas of biology, including tumorigenesis, metabolism, and even neurobiology. However, one of the major barriers for understanding human immunological mechanisms is that immune assays have not been reproducibly characterized for a sufficiently large and diverse healthy human cohort. Here, we present the 10,000 Immunomes Project (10KIP), a framework for growing a diverse human immunology reference, from ImmPort, a publicly available resource of subject-level immunology data. Although some measurement types are sparse in the presently deposited ImmPort database, the extant data allow for a diversity of robust comparisons. Using 10KIP, we describe variations in serum cytokines and leukocytes by age, race, and sex; define a baseline cell-cytokine network; and describe immunologic changes in pregnancy. All data in the resource are available for visualization and download at http://10kimmunomes.org/.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263160PMC
http://dx.doi.org/10.1016/j.celrep.2018.09.021DOI Listing

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