Fukushima J. Med. Sci.,
Vol. 52, No. 2, 2006

[Original Article]

POSSIBLE ASSOCIATION OF CYTOTOXIC T LYMPHOCYTE ANTIGEN-4
GENETIC POLYMORPHISM WITH LIVER DAMAGE
OF PRIMARY BILIARY CIRRHOSIS IN JAPAN

YUKIKO KANNO, TSUYOSHI RAI, KYOKO MONOE, HIRONOBU SAITO,
ATSUSHI TAKAHASHI, ATSUSHI IRISAWA and HIROMASA OHIRA

Department of Internal Medicine II, Fukushima Medical University School of Medicine,
Fukushima, 960-1295, Japan

(Received June 12, 2006, accepted August 17, 2006)

Abstract: Cytotoxic T lymphocyte antigen-4 (CTLA-4) is an important inhibitor of T-lymphocyte response. Polymorphisms in the CTLA-4 gene have been reported to be associated with numerous autoimmune diseases. The aim of this study was to determine whether polymorphisms of CTLA-4 exon 1 (+49) genes are associated with susceptibility and clinicolaboratory findings of primary biliary cirrhosis (PBC) in the Japanease population. Blood samples were obtained from 45 patients (6 men and 39 women, aged 23-56 years) with PBC and 73 healthy controls (48 men and 25 women, aged 22-72 years). CTLA-4 exon 1 (+49) polymorphism was defined using a polymerase chain reaction-restriction fragment length polymorphism with Bst71I restriction enzyme. The genotype frequencies of A/A, A/G, and G/G in 45 patients with PBC were 11% (5 patients), 44% (20 patients), and 44% (20 patients), respectively. There was no significant difference between frequencies in PBC patients and healthy controls. PBC patients with G/G genotype had significantly higher serum levels of ALT, GGT, and IgM than those in patients with A/A or A/G genotype. In conclusion, CTLA-4 gene polymorphisms are not associated with susceptibility of PBC in Japan; however, G/G genotype may be associated with liver damage.

Key words: Cytotoxic T lymphocyte antigen-4, polymorphysm, primary biliary cirrhosis



›–ė—L‹IŽqC—‹@@‹BC•Ļ]‹ąŽqCÄ“ĄLMC‚‹ī“ÖŽjC“üāV“ÄŽuC‘å•―Oģ

Correspondence to: Hiromasa Ohira, Department of Internal Medicine II, Fukushima Medical University School of Medicine, Fukushima City 960-1295, Japan.
E-mail: h-ohira@fmu.ac.jp