Phenotypic Characteristics of PD-1 and CTLA-4 Expression in Symptomatic Acute Hepatitis A

被引:14
作者
Cho, Hyosun [1 ]
Kang, Hyojeung [2 ]
Kim, Chang Wook [3 ]
Kim, Hee Yeon [3 ]
Jang, Jeong Won [3 ]
Yoon, Seung Kew [3 ]
Lee, Chang Don [3 ]
机构
[1] Duksung Womens Univ, Coll Pharm, Dept Pharm, Seoul, South Korea
[2] Kyungpook Natl Univ, Coll Pharm, Dept Pharm, Daegu, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Internal Med, Seoul, South Korea
关键词
Acute hepatitis A; Cytotoxic T lymphocyte-associated antigen 4; Programmed death 1; CD8(+) T-CELLS; INFECTION; VIRUS; PATHWAYS; BLOCKADE;
D O I
10.5009/gnl14368
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The immunoregulatory molecules programmed death 1 (PD-1) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) are associated with the dysfunction of antiviral effector T-cells, which leads to T-cell exhaustion and persistent viral infection in patients with chronic hepatitis C and chronic hepatitis B. Little is known about the role of PD-1 and CTLA-4 in patients with symptomatic acute hepatitis A (AHA). Methods: Peripheral blood mononuclear cells were isolated from seven patients with AHA and from six patients with nonviral acute toxic hepatitis (ATH) during the symptomatic and convalescent phases of the respective diseases; five healthy subjects acted as controls. The expression of PD-1 and CTLA-4 on T-cells was measured by flow cytometry. Results: PD-1 and CTLA-4 expression during the symptomatic phase was significantly higher in the T cells of AHA patients than in those of ATH patients or healthy controls (PD-1:18.3% vs 3.7% vs 1.6%, respectively, p<0.05; CTLA-4: 23.5% vs 6.1% vs 5.9%, respectively, p<0.05). The levels of both molecules decreased dramatically during the convalescent phase of AHA, whereas a similar pattern was not seen in ATH. Conclusions: Our findings are consistent with a viral-protective effect of PD-1 and CTLA-4 as inhibitory molecules that suppress cytotoxic T-cells and thereby prevent the destruction of virus-infected hepatocytes in AHA.
引用
收藏
页码:288 / 294
页数:7
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