Kynurenic acid may underlie sex-specific immune responses to COVID-19

Jul 6, 2021·
Yuping Cai
,
Daniel J. Kim
,
Takehiro Takahashi
,
David I. Broadhurst
Hong Yan
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
,
Yale IMPACT Research Team
,
Albert I. Ko
Sajid A. Khan
Sajid A. Khan
Akiko Iwasaki
Akiko Iwasaki
Caroline H. Johnson
Caroline H. Johnson
· 1 min read

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.

Publication

Science Signaling

Type

Journal Articles

Hong Yan
Authors
Research Assistant Professor
Sajid A. Khan
Authors
Sajid A. Khan
Associate Professor
Yale University
Akiko Iwasaki
Authors
Akiko Iwasaki
Sterling Professor
Yale University
Caroline H. Johnson
Authors
Caroline H. Johnson
Associate Professor
Yale University