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. 2023 Feb;58(2):112-124.
doi: 10.1007/s00535-022-01933-0. Epub 2022 Oct 27.

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

Affiliations

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

Lusheng Song et al. J Gastroenterol. 2023 Feb.

Abstract

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/Tipα [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/Tipα [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.

Keywords: H. pylori; Intestinal metaplasia; NAPPA; Premalignant lesions; Serology.

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Conflict of interest statement

The authors have no relevant financial or nonfinancial interests to disclose.

Figures

Fig. 1
Fig. 1
Pairwise Pearson correlations (ranged from − 0.20 to 0.56) among the 11 validated anti-H. pylori IgG and 2 IgA antibodies differential between gastric intestinal metaplasia cases and non-atrophic gastritis controls in the validation sample set. All pairwise comparisons with correlations higher than 0.2 were statistically significant with p values < 0.01
Fig. 2
Fig. 2
Pairwise Pearson correlations (ranged from − 0.06 to 0.53) among the 15 validated anti-H. pylori IgG and 1 IgA antibodies differential between current and past H. pylori infection in the validation sample set. All pairwise comparisons with correlations higher than 0.2 were statistically significant with p values < 0.01

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