Authors
Yuping Cai
Daniel J. Kim
Takehiro Takahashi
David I. Broadhurst, Edith Cowan UniversityFollow
Hong Yan
Shuangge Ma
Nicholas J. W. Rattray
Arnau Casanovas-Massana
Benjamin Israelow
Jon Klein
Carolina Lucas
Tianyang Mao
Adam J. Moore
M. Catherine Muenker
Ji Eun Oh
Julio Silva
Patrick Wong
Albert I. Ko
Sajid A. Khan
Akiko Iwasaki
Caroline H. Johnson
Yale IMPACT Research team
Document Type
Journal Article
Publication Title
Science Signaling
Volume
14
Issue
690
Publisher
American Association for the Advancement of Science
School
School of Science / Centre for Integrative Metabolomics and Computational Biology
RAS ID
36885
Abstract
Coronavirus disease 2019 (COVID-19) has poorer clinical outcomes in males than in females, and immune responses underlie these sex-related differences. Because immune responses are, in part, regulated by metabolites, we examined the serum metabolomes of COVID-19 patients. In male patients, kynurenic acid (KA) and a high KA–to–kynurenine (K) ratio (KA:K) positively correlated with age and with inflammatory cytokines and chemokines and negatively correlated with T cell responses. Males that clinically deteriorated had a higher KA:K than those that stabilized. KA inhibits glutamate release, and glutamate abundance was lower in patients that clinically deteriorated and correlated with immune responses. Analysis of data from the Genotype-Tissue Expression (GTEx) project revealed that the expression of the gene encoding the enzyme that produces KA, kynurenine aminotransferase, correlated with cytokine abundance and activation of immune responses in older males. This study reveals that KA has a sex-specific link to immune responses and clinical outcomes in COVID-19, suggesting a positive feedback between metabolites and immune responses in males.
DOI
10.1126/scisignal.abf8483
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
Comments
Cai, Y., Kim, D. J., Takahashi, T., Broadhurst, D. I., Yan, H., Ma, S., ... Iwasaki, A. (2021). Kynurenic acid may underlie sex-specific immune responses to COVID-19. Science Signaling, 14(690), Article eabf8483.
https://doi.org/10.1126/scisignal.abf8483