Normative dataset for plasma cytokines in healthy human adults.
Abstract
We determined normative data for plasma cytokines established from a cohort of 126
carefully screened healthy adults aged 18 to 64 years. Participants were enrolled
to ensure an even age and sex distribution and to include at least 30% non-Caucasians.
Plasma cytokines for 18 analytes were tested by multiplex immunoassay. The data are
presented by age cohort (18-29 years, 30-39, 40-49, and 50-66), as well as by sex
and racial background. This dataset complements published normative ranges of cellular
subsets generated by comprehensive polychromatic flow cytometry analysis of the healthy
human immune system [1]. These data are available to researchers and have value as
a reference range for research involving peripheral cytokines.
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https://hdl.handle.net/10161/22466Published Version (Please cite this version)
10.1016/j.dib.2021.106857Publication Info
(2021). Normative dataset for plasma cytokines in healthy human adults. Data in brief, 35. pp. 106857. 10.1016/j.dib.2021.106857. Retrieved from https://hdl.handle.net/10161/22466.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Jeffrey Guptill
Associate Professor of Neurology
Kent James Weinhold
Joseph W. and Dorothy W. Beard Distinguished Professor of Experimental Surgery, in
the School of Medicine
In addition to their ongoing HIV/AIDS-related research activities, the Weinhold Laboratory
is focused on utilizing a comprehensive repertoire of highly standardized and formerly
validated assay platforms to profile the human immune system in order to identify
immunologic signatures that predict disease outcomes. These ongoing studies span a
broad range of highly relevant clinical arenas, including: 1) cancer (non-small cell
lung cancer, head and neck cancer, glioblastoma neof
John S Yi
Adjunct Assistant Professor in the Department of Surgery
I am an immunologist, with a focus to characterize the immune system in response to
infectious and non-infectious diseases including cancer, HIV, autoimmune disease,
and transplantation. My goals are to identify novel biomarkers/immune signatures that
clinicians can utilize to diagnosis, predict disease outcomes, and determine patients'
response to treatment.
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