The expression of CD86 in CD3+CD56+ NKT cells is associated with the occurrence and prognosis of sepsis-associated encephalopathy in sepsis patients: a prospective observational cohort study

The role of CD3 + CD56 + natural killer T (NKT) cells and its co-signaling molecules in patients with sepsis-associated encephalopathy (SAE) is unknown. In this prospective observational cohort study, we initially recruited 260 septic patients and eventually analyzed 90 patients, of whom 57 were in...

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Veröffentlicht in:Immunologic research 2023-12, Vol.71 (6), p.929-940
Hauptverfasser: Chen, Sheng-long, Liu, Xiao-yu, Huang, Jun-hong, Xian, Lu-hua, Li, Xu-sheng, Wang, Kang-rong, Li, Jing, Zhang, Tian-cao, Huang, Guo-ge, Liu, Xin-qiang, Zeng, Hong-ke, Zhou, Mao-hua, Jiang, Wen-qiang
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Sprache:eng
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Zusammenfassung:The role of CD3 + CD56 + natural killer T (NKT) cells and its co-signaling molecules in patients with sepsis-associated encephalopathy (SAE) is unknown. In this prospective observational cohort study, we initially recruited 260 septic patients and eventually analyzed 90 patients, of whom 57 were in the SAE group and 37 were in the non-SAE group. Compared to the non-SAE group, 28-day mortality was significantly increased in the SAE group (33.3% vs. 12.1%, p  = 0.026), while the mean fluorescence intensity (MFI) of CD86 in CD3 + CD56 + NKT cells was significantly lower (2065.8 (1625.5 ~ 3198.8) vs. 3117.8 (2278.1 ~ 5349), p  = 0.007). Multivariate analysis showed that MFI of CD86 in NKT cells, APACHE II score, and serum albumin were independent risk factors for SAE. Furthermore, the Kaplan–Meier survival analysis indicated that the mortality rate was significantly higher in the high-risk group than in the low-risk group ( χ 2  = 14.779, p  
ISSN:0257-277X
1559-0755
DOI:10.1007/s12026-023-09405-0