TY - JOUR
T1 - Eccrine Sweat as a Biofluid for Profiling Immune Biomarkers
AU - Katchman, Benjamin A.
AU - Zhu, Meilin
AU - Blain Christen, Jennifer
AU - Anderson, Karen
N1 - Funding Information:
The authors gratefully acknowledge funding from the NSF/NIH Smart and Connected Research Grant (IIS-1521904).
Publisher Copyright:
© 2018 The Authors. Proteomics – Clinical Application Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2018/11
Y1 - 2018/11
N2 - Purpose: Sweat is a relatively unexplored biofluid for diagnosis and monitoring of disease states. In this study, the proteomic profiling of immune-related biomarkers from healthy individuals are presented. Experimental Design: Eccrine sweat samples are collected from 50 healthy individuals. LC-MS/MS is performed on two pools of sweat samples from five male and female participants. Individual sweat samples are analyzed by antibody isotyping microarrays (n = 49), human cytokine arrays (n = 30), and quantitative ELISAs for interleukin-1α (n = 16), epidermal growth factor (n = 6), and angiogenin (n = 7). Results: In sweat, 220 unique proteins are identified by shotgun analysis. Detectable antibody isotypes include IgA (100% positive; median 1230 ± 28 700 pg mL −1 ), IgD (18%; 22.0 ± 119 pg mL −1 ), IgG1 (96%; 1640 ± 6750 pg mL −1 ), IgG2 (37%; 292 ± 6810 pg mL −1 ), IgG3 (71%; 74.0 ± 119 pg mL −1 ), IgG4 (69%; 43.0 ± 42.0 pg mL −1 ), and IgM (41%; 69.0 ± 1630 pg mL −1 ). Of 42 cytokines, three are readily detected in all sweat samples (p < 0.01). The median concentration for interleukin-1α is 352 ± 521 pg mL −1 , epidermal growth factor is 86.5 ± 147 pg mL −1 , and angiogenin is 38.3 ± 96.3 pg mL −1 . Multiple other cytokines are detected at lower levels. Conclusions and Clinical Relevance: Sweat can be used for profiling antibodies and innate immune biomarkers.
AB - Purpose: Sweat is a relatively unexplored biofluid for diagnosis and monitoring of disease states. In this study, the proteomic profiling of immune-related biomarkers from healthy individuals are presented. Experimental Design: Eccrine sweat samples are collected from 50 healthy individuals. LC-MS/MS is performed on two pools of sweat samples from five male and female participants. Individual sweat samples are analyzed by antibody isotyping microarrays (n = 49), human cytokine arrays (n = 30), and quantitative ELISAs for interleukin-1α (n = 16), epidermal growth factor (n = 6), and angiogenin (n = 7). Results: In sweat, 220 unique proteins are identified by shotgun analysis. Detectable antibody isotypes include IgA (100% positive; median 1230 ± 28 700 pg mL −1 ), IgD (18%; 22.0 ± 119 pg mL −1 ), IgG1 (96%; 1640 ± 6750 pg mL −1 ), IgG2 (37%; 292 ± 6810 pg mL −1 ), IgG3 (71%; 74.0 ± 119 pg mL −1 ), IgG4 (69%; 43.0 ± 42.0 pg mL −1 ), and IgM (41%; 69.0 ± 1630 pg mL −1 ). Of 42 cytokines, three are readily detected in all sweat samples (p < 0.01). The median concentration for interleukin-1α is 352 ± 521 pg mL −1 , epidermal growth factor is 86.5 ± 147 pg mL −1 , and angiogenin is 38.3 ± 96.3 pg mL −1 . Multiple other cytokines are detected at lower levels. Conclusions and Clinical Relevance: Sweat can be used for profiling antibodies and innate immune biomarkers.
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U2 - 10.1002/prca.201800010
DO - 10.1002/prca.201800010
M3 - Article
C2 - 29882373
AN - SCOPUS:85056576545
SN - 1862-8346
VL - 12
JO - Proteomics - Clinical Applications
JF - Proteomics - Clinical Applications
IS - 6
M1 - 1800010
ER -