Identification of anti-Helicobacter pylori antibody signatures in gastric intestinal metaplasia

被引:10
作者
Song, Lusheng [1 ]
Song, Minkyo [2 ]
Rabkin, Charles S. [2 ]
Chung, Yunro [1 ,3 ]
Williams, Stacy [1 ]
Torres, Javier [4 ]
Corvalan, Alejandro H. [5 ,6 ]
Gonzalez, Robinson [5 ,6 ]
Bellolio, Enrique [7 ,8 ]
Shome, Mahasish [1 ]
LaBaer, Joshua [1 ]
Qiu, Ji [1 ]
Camargo, M. Constanza [2 ]
机构
[1] Arizona State Univ, Virginia G Piper Ctr Personalized Diagnost, Biodesign Inst, 1001 S McAllister Ave,POB 876401, Tempe, AZ 85287 USA
[2] NCI, Div Canc Epidemiol & Genet, Rockville, MD USA
[3] Arizona State Univ, Coll Hlth Solut, Phoenix, AZ USA
[4] Inst Mexicano Seguro Social, Unidad Invest Enfermedades Infecciosas, UMAE Pediat, Mexico City, DF, Mexico
[5] Pontificia Univ Catolica Chile, Fac Med, Santiago, Chile
[6] Pontificia Univ Catolica Chile, Adv Ctr Chron Dis, Santiago, Chile
[7] Hosp Dr Hernan Henriquez Aravena, Temuco, Chile
[8] Univ La Frontera, Dept Anat Patol, Temuco, Chile
关键词
Intestinal metaplasia; H; pylori; NAPPA; Serology; Premalignant lesions; PROTEIN; INFECTION; CARCINOGENESIS; DIAGNOSIS; SEROLOGY; SOCIETY; LESIONS; ALPHA; RISK;
D O I
10.1007/s00535-022-01933-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Chronic Helicobacter pylori infection may induce gastric intestinal metaplasia (IM). We compared anti-H. pylori antibody profiles between IM cases and non-atrophic gastritis (NAG) controls. Methods We evaluated humoral responses to 1528 H. pylori proteins among a discovery set of 50 IM and 50 NAG using H. pylori protein arrays. Antibodies with >= 20% sensitivity at 90% specificity for either group were selected and further validated in an independent set of 100 IM and 100 NAG using odds ratios (OR). A validated multi-signature was evaluated using the area under the receiver operating characteristics curve (AUC) and net reclassification improvement (NRI). Results Sixty-two immunoglobulin (Ig) G and 11 IgA antibodies were detected in > 10%. Among them, 22 IgG and 6 IgA antibodies were different between IM and NAG in the discovery set. Validated antibodies included 11 IgG (anti-HP1177/Omp27/HopQ [OR = 8.1, p < 0.001], anti-HP0547/CagA [4.6, p < 0.001], anti-HP0596/Tip alpha [4.0, p = 0.002], anti-HP0103/TlpB [3.8, p = 0.001], anti-HP1125/PalA/Omp18 [3.1, p = 0.001], anti-HP0153/RecA [0.48, p = 0.03], anti-HP0385 [0.41, p = 0.006], anti-HP0243/TlpB [0.39, p = 0.016], anti-HP0371/FabE [0.37, p = 0.017], anti-HP0900/HypB/AccB [0.35, p = 0.048], and anti-HP0709 [0.30, p = 0.003]), and 2 IgA (anti-HP1125/PalA/Omp18 [2.7, p = 0.03] and anti-HP0596/Tip alpha [2.5, p = 0.027]). A model including all 11 IgG antibodies (AUC = 0.81) had better discriminated IM and NAG compared with an anti-CagA only (AUC = 0.77) model (NRI = 0.44; p = 0.001). Conclusions Our study represents the most comprehensive assessment of anti-H. pylori antibody profiles in IM. The target antigens for these novel antibodies may act together with CagA in the progression to IM. Along with other biomarkers, specific H. pylori antibodies may identify IM patients, who would benefit from surveillance.
引用
收藏
页码:112 / 124
页数:13
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