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PD-1-mediated CD4+ T cell exhaustion exacerbates gut microbiota translocation in mouse model of sepsis
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Bin QING1, Xinxin KONG1, Dongfan YE1, Chuangye WANG1, Jian ZHANG1, Bin WANG1, Xiaoou HUANG1, Nanbo WANG1, Hang QIAN1, Zhi XU1, 2
Journal of Army Medical University | 2025, 47(19) : 2302 - 2314
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Journal of Army Medical University | 2025, 47(19): 2302-2314
• Military Medicine •
PD-1-mediated CD4+ T cell exhaustion exacerbates gut microbiota translocation in mouse model of sepsis
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Bin QING1, Xinxin KONG1, Dongfan YE1, Chuangye WANG1, Jian ZHANG1, Bin WANG1, Xiaoou HUANG1, Nanbo WANG1, Hang QIAN1, Zhi XU1, 2
Affiliations
  • 1Department of Respiratory and Critical Care Medicine,Chongqing Key Laboratory of Precision Medicine and Prevention of Major Respiratory Diseases,Key Laboratory of Respiratory Disease Research of Institutions of Higher Education in Chongqing,Second Affiliated Hospital,Army Medical University (Third Military Medical University),Chongqing
  • 2Yu-Yue Pathology Scientific Research Center,Chongqing,China
Published: 2025-10-15 doi: 10.16016/j.2097-0927.202507039
Outline
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Objective

To investigate the characteristics of immune exhaustion in sepsis and analyze its association with gut microbiota translocation.

Methods

A total of 130 mice were randomly divided into a cecal ligation and puncture (CLP) group (n=100) and a Sham group (n=30) Mouse model of sepsis was established with CLP procedure. Flow cytometry was used to analyze the proportions of peripheral blood CD4+ T and CD8+T cells and programmed cell death protein 1 (PD-1) positive T cell subsets in mice. Bacterial colonization in organs such as the heart, liver and kidneys was quantified by plating homogenates of the organs. Pathological changes in immune organs were observed with HE staining. The expression and localization of CD4⁺, CD8⁺, and PD-1⁺cells in immune organs were detected with immunohistochemical staining, and Image J software was employed for subsequent quantification of the number of the positive cells.

Results

HE staining demonstrated that immune organs exhibited varying degrees of pathological damages with disease progression. Compared with the Sham mice, the CLP mice exhibited significantly increased bacterial colonization in parenchymal organs and peripheral blood (P<0.05), notably in the liver, which showed the most severe infection. In the CLP group, the proportion of CD4+ T lymphocytes in peripheral blood at days 1, 3, and 5 postoperatively was decreased by 56%, 70.57%, and 87.42%, respectively, when compared with the Sham group (P<0.001). The proportion of CD8+ T lymphocytes was decreased by 48.33% relative to the Sham group only at day 5 (P<0.001). In contrast, the proportion of CD4+ T cell subsets expressing PD-1 was increased to 673.08, 423.08, and 600 times that of the Sham group, respectively, at the same postoperative time points (P<0.001). Immunohistochemical results showed that, in the CLP group, the proportion of CD4+ T cells in the thymus, spleen, and mesenteric lymph nodes was increased to 7.65, 2.66, and 3.7 times that of the Sham group, respectively, at the early-stage peak (P<0.001), and then these proportions were decreased by 82.8% (P<0.001), 41.9% (P<0.01), and 60.15% (P<0.001), respectively, at the late-stage trough when compared with the early-stage peak in the corresponding organs. The proportion of CD8+ positive cells was increased in the early stage and then decreased insignificantly, while the proportion of PD-1+ positive cells was increased continuously, and reached 6.24, 13.9, and 20.96 times that of the Sham group at the peak in the thymus, spleen, and mesenteric lymph nodes respectively (P<0.001), with their expression regions showing a rough overlap with those of CD4+ cells.

Conclusion

During sepsis, the inflammatory response can cause severe damage to immune organs and persistent exhaustion of CD4⁺T lymphocytes, leading to declined defenses against infection, which may be the main causes for exacerbated gut microbiota translocation and then systemic infection.

sepsis  /  bacterial translocation  /  T cell exhaustion  /  programmed cell death protein 1
卿斌, 孔鑫鑫, 叶东樊, 王创业, 张健, 王斌, 黄小鸥, 王南博, 钱航, 徐智. PD-1介导的CD4+ T细胞耗竭加剧脓毒症小鼠的肠道菌群异位. 陆军军医大学学报, 2025 , 47 (19) : 2302 -2314 . DOI: 10.16016/j.2097-0927.202507039
Bin QING, Xinxin KONG, Dongfan YE, Chuangye WANG, Jian ZHANG, Bin WANG, Xiaoou HUANG, Nanbo WANG, Hang QIAN, Zhi XU. PD-1-mediated CD4+ T cell exhaustion exacerbates gut microbiota translocation in mouse model of sepsis[J]. Journal of Army Medical University, 2025 , 47 (19) : 2302 -2314 . DOI: 10.16016/j.2097-0927.202507039
Year 2025 volume 47 Issue 19
27
10
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doi: 10.16016/j.2097-0927.202507039
  • Receive Date:2025-07-12
  • Online Date:2026-10-30
  • Published:2025-10-15
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History
  • Received:2025-07-12
  • Revised:2025-09-12
Affiliations
    1Department of Respiratory and Critical Care Medicine,Chongqing Key Laboratory of Precision Medicine and Prevention of Major Respiratory Diseases,Key Laboratory of Respiratory Disease Research of Institutions of Higher Education in Chongqing,Second Affiliated Hospital,Army Medical University (Third Military Medical University),Chongqing
    2Yu-Yue Pathology Scientific Research Center,Chongqing,China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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