LOXL-2 and TNC-C are markers of liver fibrogenesis in HCV/HIV-, HIV- and HCV-infected patients

Author:

Altinbas Akif1ORCID,Holmes Jacinta A1,Salloum Shadi1,Lidofsky Anna1ORCID,Alatrakchi Nadia1,Somsouk Ma2ORCID,Hunt Peter2ORCID,Deeks Steven2ORCID,Chew Kara W3,Lauer Georg1,Kruger Annie1ORCID,Lin Wenyu1ORCID,Chung Raymond T1

Affiliation:

1. Department of Medicine, Harvard Medical School & Massachusetts General Hospital, Boston, MA 02114, USA

2. Department of Medicine, University of California San Francisco, School of Medicine, San Francisco, CA 94143, USA

3. Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA

Abstract

Background: Lysil oxidase like enzyme-2 (LOXL-2) and TNC-C play important roles in organ fibrosis. We assessed circulating LOXL-2 and TNC-C levels and their relationship to fibrosis severity in HIV- and/or HCV-infected individuals. Methods: Healthy controls (n = 22), HIV mono- (n = 15), HCV mono- (n = 52) and HCV/HIV-co-infected (n = 92) subjects were included. Results: LOXL-2 and TNC-C levels were significantly higher in HCV mono- and HCV/HIV-co-infected individuals with F0 compared to healthy controls. In addition, in HCV/HIV-co-infected individuals, LOXL-2 levels were higher in intermediate fibrosis compared to no/mild fibrosis. Conclusion: In HCV/HIV-co-infected study participants, both LOXL-2 and TNC-C were significantly higher in intermediate fibrosis compared to no/mild fibrosis, but did not further increase with advanced fibrosis. Furthermore, both markers were elevated among HCV/HIV-positive individuals with mild/no fibrosis.

Funder

Center for AIDS Research, University of California, San Diego

Foundation for the National Institutes of Health

Gladstone Institutes

Publisher

Future Medicine Ltd

Subject

Biochemistry (medical),Clinical Biochemistry,Drug Discovery

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Emerging mechanisms of non-alcoholic steatohepatitis and novel drug therapies;Chinese Journal of Natural Medicines;2024-08

2. A virological view of tenascin-C in infection;American Journal of Physiology-Cell Physiology;2023-01-01

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