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Deficiency in Peripheral MAIT Cells But Not in Intrahepatic MAIT Cells in Humans with CHBV Infection

33 Pages Posted: 25 Jun 2019

See all articles by Wenyong Huang

Wenyong Huang

Sun Yat-sen University (SYSU) - Organ Transplantation Center

Wenjing He

Sun Yat-sen University (SYSU) - Organ Transplantation Center

Xiaomin Shi

Sun Yat-sen University (SYSU) - Organ Transplantation Center

Qianyu Ye

Sun Yat-sen University (SYSU) - Organ Transplantation Center

Xiaoshun He

Sun Yat-sen University (SYSU) - Department of Organ Transplantation

Lang Dou

Sun Yat-sen University (SYSU) - Organ Transplantation Center

Yifang Gao

Sun Yat-sen University (SYSU) - Organ Transplantation Center; Sun Yat-sen University (SYSU) - Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology

More...

Abstract

Background: Chronic hepatitis B virus (CHBV) infection is a major cause of liver diseases. Mucosal-associated invariant T (MAIT) cells are important for antiviral immunity in the liver, but the distinction between intrasinusoidal MAIT cells and peripheral MAIT cells in patients with CHBV infection remains unclear.

Methods: PBMC were obtained from patients with CHBV infection (n=51) and age-matched controls (n=52). Liver-associated mononuclear cells (LMCs) were collected from donors (n=32) and explanted liver (n=23) of patients to perform phenotypic, functional and TCR diversity analysis.

Results: The frequency of intrasinusoidal MAIT cells in the CHBV infection group was not changed compared to that of the MAIT cells in the CHBV-negative group. However, the frequency of peripheral blood MAIT cells was severely reduced in the CHBV infection group compared to the CHBV-negative group. Moreover, IFN-γ production was intact in the intrahepatic MAIT cells of the CHBV infection patients compared to those of the control subjects post IL-12 and IL-18 stimulation, while it was reduced in the peripheral blood MAIT cells of the CHBV infection patients. More importantly, our study showed that the expression level of HLA-DR in peripheral MAIT cells was higher than that in intrasinusoidal MAIT cells in CHBV infection patients. A distinct signature of TCR usage was found in the CHBV patients.

Conclusions: By analysing the phenotype, function and TCR usage of MAIT cells in the PBMC and LMC populations of patients with CHBV infection, we found distinct functions and activities in the MAIT cells of the liver compared with those of the peripheral blood.

Funding Statement: YG is supported by Natural Science Foundation of Guangdong Province (Grant number: 2018A030313019) and National Natural Science Foundation of China (Grant number:31800758).

Declaration of Interests: All authors disclose no conflicts of interest.

Ethics Approval Statement: This study was fully approved by the First Affiliated Hospital of Sun Yat-sen University ethical board. All participants provided written informed consent before sample collection.

Keywords: MAIT cells, Chronic hepatitis B virus, Liver

Suggested Citation

Huang, Wenyong and He, Wenjing and Shi, Xiaomin and Ye, Qianyu and He, Xiaoshun and Dou, Lang and Gao, Yifang, Deficiency in Peripheral MAIT Cells But Not in Intrahepatic MAIT Cells in Humans with CHBV Infection (06/21/2019 03:39:23). Available at SSRN: https://ssrn.com/abstract=3408075 or http://dx.doi.org/10.2139/ssrn.3408075

Wenyong Huang

Sun Yat-sen University (SYSU) - Organ Transplantation Center

China

Wenjing He

Sun Yat-sen University (SYSU) - Organ Transplantation Center

China

Xiaomin Shi

Sun Yat-sen University (SYSU) - Organ Transplantation Center

China

Qianyu Ye

Sun Yat-sen University (SYSU) - Organ Transplantation Center

China

Xiaoshun He

Sun Yat-sen University (SYSU) - Department of Organ Transplantation ( email )

Guangzhou
China

Lang Dou

Sun Yat-sen University (SYSU) - Organ Transplantation Center

China

Yifang Gao (Contact Author)

Sun Yat-sen University (SYSU) - Organ Transplantation Center ( email )

China

Sun Yat-sen University (SYSU) - Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology ( email )

China

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