Increased serum GM-CSF at diagnosis of biliary atresia is associated with improved biliary drainage

被引:0
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作者
Taylor, Sarah A. [1 ,2 ]
Harpavat, Sanjiv [3 ]
Gromer, Kyle D. [4 ]
Andreev, Victor [5 ]
Loomes, Kathleen M. [6 ]
Bezerra, Jorge A. [7 ,8 ]
Jarasvaraparn, Chaowapong [9 ]
Wang, Kasper [10 ,11 ]
Horslen, Simon [12 ]
Rosenthal, Philip [13 ]
Teckman, Jeffrey [14 ]
Valentino, Pamela L. [15 ]
Ng, Vicky L. [11 ]
Karpen, Saul J. [16 ,17 ]
Sokol, Ronald J. [1 ,2 ]
Alonso, Estella M. [4 ]
Mack, Cara L. [18 ]
机构
[1] Childrens Hosp Colorado, Dept Pediat, Aurora, CO 80129 USA
[2] Univ Colorado, Sch Med, Aurora, CO 80045 USA
[3] Texas Childrens Hosp, Dept Pediat, Houston, TX USA
[4] Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pediat, Chicago, IL USA
[5] Arbor Res Collaborat Hlth, Ann Arbor, MI USA
[6] Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA USA
[7] Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Cincinnati, OH USA
[8] UT Southwestern Med Ctr, Dept Pediat, Dallas, TX USA
[9] Riley Hosp Children, Dept Pediat, Indianapolis, IN USA
[10] Childrens Hosp Los Angeles, Dept Surg, Los Angeles, CA USA
[11] Hosp Sick Children, Ontario, CA USA
[12] Childrens Hosp Pittsburgh, Dept Pediat, Pittsburgh, PA USA
[13] Univ Calif San Francisco, Dept Pediat & Surg, San Francisco, CA USA
[14] St Louis Univ, SSM Hlth Cardinal Glennon Childrens Hosp, Sch Med, Dept Pediat, St Louis, MO USA
[15] Seattle Childrens Hosp, Dept Pediat, Seattle, WA USA
[16] Childrens Healthcare Atlanta, Dept Pediat, Atlanta, GA USA
[17] Virginia Commonwealth Univ, Dept Pediat, Richmond, VA USA
[18] Med Coll Wisconsin, Dept Pediat, Childrens Wisconsin, Milwaukee, WI USA
关键词
LIVER; HEPATOPORTOENTEROSTOMY; PATHOGENESIS; BILIRUBIN; OUTCOMES; DISEASE;
D O I
10.1038/s41390-025-03804-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: The immune heterogeneity of biliary atresia (BA) presents a challenge for development of prognostic biomarkers. This study aimed to identify early immune signatures associated with biliary drainage after Kasai Portoenterostomy (KPE). METHODS: Serum samples, liver slides, and clinical data were obtained from patients enrolled in the NIDDK-supported Childhood Liver Disease Research Network. Serum cytokines and hepatic immune cell subsets were measured at diagnosis and compared among 3 groups: 38 infants with BA (20 with evidence of bile flow after KPE; 18 without) and 17 non-BA cholestatic infants. RESULTS: BA participants had lower numbers of lipid associated macrophages (LAM), and increased serum levels of Eotaxin-3, interleukin (IL) 12p70, and IL-8 versus non-BA groups (p < 0.05 for all). Among BA participants, monocyte like macrophages and serum levels of granulocyte-macrophage colony stimulating factor (GM-CSF) were increased in BA participants with good biliary drainage (p = 0.004 and p < 0.001 respectively). Levels of GM-CSF, IL-16, c-reactive protein, TNF-beta predicted successful biliary drainage with an area under the receiver operating curve of 0.84 (p < 0.001). CONCLUSION: These findings suggest that distinct macrophage-associated immune networks at diagnosis may impact biliary drainage after KPE. Identification of early prognostic immune-modulatory markers has potential to improve patient stratification for medical and surgical therapies.
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页数:9
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