Hepatitis B virus‐specific human stem cell memory T cells differentiate into cytotoxic T cells and eradicate HBV‐infected hepatocytes in mice

Author:

Abe‐Chayama Hiromi1ORCID,Kawase Takakazu23,Ichinohe Tatsuo3,Ishida Yuji4,Tateno Chise4,Hijikata Makoto5,Chayama Kazuaki567

Affiliation:

1. Center for Medical Specialist Graduate Education and Research, Graduate School of Biomedical and Health Sciences Hiroshima University Japan

2. Department of Immune Regenerative Medicine, International Center for Cell and Gene Therapy Fujita Health University Toyoake Japan

3. Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine (RIRBM) Hiroshima University Japan

4. PhoenixBio Co., Ltd. Hiroshima Japan

5. Hiroshima Institute of Life Sciences Japan

6. Collaborative Research Laboratory of Medical Innovation, Graduate School of Biomedical and Health Sciences Hiroshima University Japan

7. RIKEN Center for Integrative Medical Sciences Yokohama Japan

Abstract

Chronic infection with the hepatitis B virus (HBV) induces progressive hepatic impairment. Achieving complete eradication of the virus remains a formidable challenge. Cytotoxic T lymphocytes, specific to viral antigens, either exhibit a numerical deficiency or succumb to an exhausted state in individuals chronically afflicted with HBV. The comprehension of the genesis and dissemination of stem cell memory T cells (TSCMs) targeting HBV remains inadequately elucidated. We identified TSCMs in subjects with chronic HBV infection and scrutinized their efficacy in a murine model with human hepatocyte transplants, specifically the TK‐NOG mice. TSCMs were discerned in all subjects under examination. Introduction of TSCMs into the HBV mouse model precipitated a severe necro‐inflammatory response, resulting in the elimination of human hepatocytes. TSCMs may constitute a valuable tool in the pursuit of a remedial therapy for HBV infection.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Wiley

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