A genome-wide association study identified PTPN2 as a population-specific susceptibility gene locus for primary biliary cholangitis

• Published in: Hepatology (Baltimore, Md.) Vol. 80; no. 4; pp. 776 - 790
• Main Authors: Hitomi, Yuki, Ueno, Kazuko, Aiba, Yoshihiro, Nishida, Nao, Kono, Michihiro, Sugihara, Mitsuki, Kawai, Yosuke, Kawashima, Minae, Khor, Seik-Soon, Sugi, Kazuhiro, Kouno, Hirotaka, Kouno, Hiroshi, Naganuma, Atsushi, Iwamoto, Satoru, Katsushima, Shinji, Furuta, Kiyoshi, Nikami, Toshiki, Mannami, Tomohiko, Yamashita, Tsutomu, Ario, Keisuke, Komatsu, Tatsuji, Makita, Fujio, Shimada, Masaaki, Hirashima, Noboru, Yokohama, Shiro, Nishimura, Hideo, Sugimoto, Rie, Komura, Takuya, Ota, Hajime, Kojima, Motoyuki, Nakamuta, Makoto, Fujimori, Naoyuki, Yoshizawa, Kaname, Mano, Yutaka, Takahashi, Hironao, Hirooka, Kana, Tsuruta, Satoru, Sato, Takeaki, Yamasaki, Kazumi, Kugiyama, Yuki, Motoyoshi, Yasuhide, Suehiro, Tomoyuki, Saeki, Akira, Matsumoto, Kosuke, Nagaoka, Shinya, Abiru, Seigo, Yatsuhashi, Hiroshi, Ito, Masahiro, Kawata, Kazuhito, Takaki, Akinobu, Arai, Kuniaki, Arinaga, Teruko, Abe, Masanori, Harada, Masaru, Taniai, Makiko, Zeniya, Mikio, Ohira, Hiromasa, Shimoda, Shinji, Komori, Atsumasa, Tanaka, Atsushi, Ishigaki, Kazuyoshi, Nagasaki, Masao, Tokunaga, Katsushi, Nakamura, Minoru
• Format: Journal Article
• Language: English
• Published: United States 01.10.2024
• ISSN: 0270-9139; 1527-3350; 1527-3350
• DOI: 10.1097/HEP.0000000000000894

Previous genome-wide association studies (GWAS) have indicated the involvement of shared (population-non-specific) and non-shared (population-specific) susceptibility genes in the pathogenesis of primary biliary cholangitis (PBC) among European and East-Asian populations. Although a meta-analysis of these distinct populations has recently identified more than 20 novel PBC susceptibility loci, analyses of population-specific genetic architecture are still needed for a more comprehensive search for genetic factors in PBC. Protein tyrosine phosphatase non-receptor type 2 (PTPN2) was identified as a novel PBC susceptibility gene locus through a GWAS and subsequent genome-wide meta-analysis involving 2,181 cases and 2,699 controls from the Japanese population (GWAS-lead variant: rs8098858, p=2.6×10-8). In-silico and in-vitro functional analyses indicated that the risk allele of rs2292758, which is a primary functional variant, decreases PTPN2 expression by disrupting Sp1 binding to the PTPN2 promoter in T follicular helper cells (Tfh) and plasmacytoid dendritic cells (pDCs). Infiltration of PTPN2-positive T-cells and pDCs were confirmed in the portal area of the PBC-liver by immunohistochemistry. Furthermore, transcriptomic analysis of PBC-liver samples indicated the presence of a compromised negative feedback loop in-vivo between PTPN2 and IFNG in patients carrying the risk allele of rs2292758. PTPN2, a novel susceptibility gene for PBC in the Japanese population, may be involved in the pathogenesis of PBC via an insufficient negative feedback loop caused by the PTPN2 risk allele of rs2292758 in IFN signaling. This suggests that PTPN2 could be a potential molecular target for PBC treatment.