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Chinese Journal of Transplantation(Electronic Edition) ›› 2025, Vol. 19 ›› Issue (04): 237-242. doi: 10.3877/cma.j.issn.1674-3903.2025.04.005

• Original Article • Previous Articles    

Analysis of specific serum biomarkers associated with acute graft versus host disease

Heng Liu1, Tao Wu1,(), Lingling Yu1, Rui Xi1, Yaozhu Pan1, Dongfeng Mao1, Yajun Shi1, Wenhui Liu1, Hongjuan Tian1, Ying Wang1, Xiaofei Zhang1, Xi Zhang2   

  1. 1Department of Hematology, the 940th Hospital of Joint Logistic Support Force of PLA, Lanzhou 730050, China
    2Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing 400037, China
  • Received:2025-04-25 Online:2025-08-25 Published:2025-10-27
  • Contact: Tao Wu

Abstract:

Objective

To explore the correlation of IL-6, IL-8, soluble tumor necrosis factor receptor 1 (sTNFR1), regenerating islet-derived protein 3-alpha (Reg3α), soluble suppression of tumorigenesis 2 (sST2) and elafin with acute graft versus host disease (aGVHD) following allogeneic hematopoietic stem cell transplantation (allo-HSCT).

Methods

A retrospective analysis was conducted on the clinical data of 106 patients who underwent allo-HSCT in the Department of Hematology at the 940th Hospital of the Joint Logistics Support Force of PLA between January 2019 and January 2023. Forty-nine patients who developed aGVHD were assigned to the aGVHD group, while 57 patients without aGVHD were included in the non-aGVHD group. Peripheral blood samples were collected from all patients at post-transplantation days + 28, + 56, and + 90 for cytokine quantification. Intergroup comparisons of normally distributed continuous variables were performed using the independent samples t-test. The Mann-Whitney U test was employed for non-normally distributed continuous variables. Categorical variables were compared using the chi-square test. A P-value < 0.05 was considered statistically significant.

Results

At days + 28, sST2 level was significantly lower in the non-aGVHD group [52.2 (34.9-93.0) pg/mL] compared to the aGVHD group [98.2 (58.3-186.7) pg/mL], Z=-3.268, P < 0.05. At days + 56, the non-aGVHD group exhibited significantly reduced level of sTNFR1 [1 971.2 (1 656.8-2 537.0) pg/mL], sST2 [76.4 (40.0-134.4) pg/mL], and Reg3α [38.8 (23.8-92.6) pg/mL] relative to the aGVHD group [sTNFR1 2 791.2 (1 698.4-3 468.2) pg/mL, sST2 191.0 (113.5-620.2) pg/mL, Reg3α 77.0 (41.5-162.0) pg/mL], Z=-2.926, -4.420 and -3.393, all P < 0.05. At days + 90, the sST2 level was lower in the non-aGVHD group [78.6 (51.0-107.1) pg/mL] than the aGVHD group [146.9 (81.0-327.8) pg/mL], Z=-3.578, P<0.05. Patients with grade Ⅱ-Ⅳ aGVHD demonstrated significantly elevated sTNFR1 level at days + 56 [3 245.4 (2 804.6-3 557.6) pg/mL] and days + 90 [2 891.2 (2 024.6-4 534.0) pg/mL], as well as higher Reg3α level at days + 56 [162.0 (65.4-310.3) pg/mL] and days + 90 [92.5 (58.1-157.7) pg/mL] compared to those with grade Ⅰ aGVHD [sTNFR1 2 009.7 (1 599.5-3 259.1) pg/mL at days + 56, 1 870.9 (1 620.2-2 334.4) pg/mL at days + 90, Reg3α 53.7 (33.2-79.7) pg/mL at days + 56, 43.9 (39.2-64.7) pg/mL at days + 90], Z=-2.639, -2.242, -3.026 and -2.743, all P<0.05. Additionally, elafin level was significantly higher in the grade Ⅱ-Ⅳ aGVHD group [14.0 (10.3-24.7) pg/mL] versus the grade Ⅰ group [8.4 (7.5-14.3) pg/mL] at days + 90 (Z=-2.162, P<0.05). Patients in the gastrointestinal aGVHD group exhibited significantly increased Reg3α level at days + 28 [94.7 (27.9-307.8) pg/mL], days + 56 [306.4 (162.1-524.4) pg/mL], and days + 90 [124.5 (70.1-312.8) pg/mL] compared to those in the non-gastrointestinal aGVHD group [33.5 (19.6-57.3), 53.8 (33.8-81.7) and 43.9 (37.6-66.7) pg/mL, respectively], Z= -2.352, -3.857 and -2.800, all P<0.05. Similarly, sTNFR1 level significantly elevated in the gastrointestinal aGVHD group at days + 56 [3 250.5 (2 980.8-4 413.2) pg/mL] and days + 90 [4 534.0 (2 419.4-6 171.2) pg/mL] relative to the non-gastrointestinal aGVHD group [2 189.4 (1 609.7-3 297.1) pg/mL and 1 885.2 (1 715.0-2 530.0) pg/mL, respectively], Z=-2.842 and -2.100, all P<0.05.

Conclusion

The serum biomarkers (sST2, sTNFR1, Reg3α and elafin) are associated with the occurrence and severity of aGVHD in patients treated with allo-HSCT, which may be valuable for clinical diagnosis and intervention.

Key words: Biomaker, Acute graft versus host disease, Allogeneic hematopoietic stem cell transplantation, Cytokine

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