Background on Helicobacter pylori

Helicobacter pylori (H. pylori) is a Gram-negative bacterium that colonizes the gastric mucosa and represents one of the most common chronic bacterial infections worldwide, with an estimated global prevalence of approximately 50%. Persistent infection has been associated with chronic gastritis, peptic ulcer disease, MALT lymphoma, and gastric adenocarcinoma. For this reason, the International Agency for Research on Cancer (IARC) of the World Health Organization (WHO) classifies H. pylori as a Group 1 carcinogen, and screening and eradication strategies are considered important measures for preventing gastric cancer.

Early diagnosis and post-treatment follow-up are essential to reduce complications and confirm eradication. Among non-invasive diagnostic methods, the detection of H. pylori stool antigen enables the identification of active infection and is widely used as a practical alternative to invasive procedures such as endoscopic biopsy.

 

Helicobacter pylori testing workflow with stool sample preparation without routine centrifugation.

Sandwich chemiluminescent immunoassay (CLIA) for the detection of Helicobacter pylori antigen in human stool samples.

  • Flexible and fully automated solution.

  • Fast and easy pre-analytical treatment, without centrifugation.

  • Simple protocol with results in 1 hour.

  • Method based upon antigen capture using monoclonal antibodies.

  • Individual quality control per monotest, no need for additional controls or calibrations.

  • Objective method with excellent diagnostic sensitivity and specificity.

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virclia monotest

Diagnostic Recommendations

Helicobacter pylori stool antigen testing

  • Results should be interpreted together with symptoms, clinical history, medication use, previous eradication therapy and other diagnostic procedures.
  • A positive stool antigen result supports detection of H. pylori antigen and is compatible with active infection.
  • A negative result does not fully exclude infection if antigen levels are below the limit of detection, the sample was not collected, stored or homogenized correctly, or testing was performed under conditions that reduce antigen detection.
  • Recent use of antibiotics, proton pump inhibitors, potassium-competitive acid blockers or bismuth-containing products may reduce H. pylori detection and lead to false-negative results.
  • Stool antigen testing can be used as a non-invasive method to support initial diagnosis and to confirm eradication after treatment.
  • Confirmation of eradication should generally be performed at least 4 weeks after treatment, after stopping PPIs or potassium-competitive acid blockers for at least 2 weeks, and antibiotics or bismuth for at least 4 weeks, when clinically feasible.
  • A positive result after treatment suggests persistent infection or treatment failure, but should be interpreted according to timing of testing, medication exposure and clinical context.
  • The assay detects H. pylori antigen and does not provide antimicrobial susceptibility information. Culture or molecular resistance testing may be required when susceptibility information is needed.
  • A positive result does not rule out other gastrointestinal conditions, co-infections or alternative causes of symptoms. Further investigation may be required according to age, alarm symptoms, risk factors and local clinical algorithms.
  • Invalid or inconclusive results should be repeated according to the laboratory procedure. If poor sample quality, incorrect storage or interference is suspected, a new stool sample should be considered.

Sources

  1. Chey WD, Howden CW, Moss SF, Morgan DR, Greer KB, Grover S, et al. ACG Clinical Guideline: Treatment of Helicobacter pylori Infection. Am J Gastroenterol. 2024;119(9):1730-1753. doi:10.14309/ajg.0000000000002968.
  2. Malfertheiner P, Megraud F, Rokkas T, Gisbert JP, Liou JM, Schulz C, et al. Management of Helicobacter pylori infection: the Maastricht VI/Florence consensus report. Gut. 2022;71(9):1724-1762. doi:10.1136/gutjnl-2022-327745.
  3. World Gastroenterology Organisation. Helicobacter pylori guideline. Milwaukee: World Gastroenterology Organisation; 2021. Available from: https://www.worldgastroenterology.org/guidelines/helicobacter-pylori

PRODUCTS

HELICOBACTER PYLORI Ag VIRCLIA® MONOTEST

CE0123 IVDR
Sandwich chemiluminescent immunoassay (CLIA) for the detection of Helicobacter pylori antigen in human stool samples.

Analytes: Helicobacter pylori

Reference VCM103 VCM103-PL
Pack size 24 test 48 test

VIRCLIA® EXTRACTION TUBE

CE IVDR
Auxiliary reagent for extraction of human stool samples tested with the VIRCLIA® kits.
Reference VCET001
Pack size 26 test

USED ON

VIRCLIA® LOTUS

virclia_lotus.jpeg

Una plataforma CLIA compacta y automatizada para los análisis VirClia® de enfermedades infecciosas, que combina la flexibilidad del formato monotest listo para usar con la eficiencia del acceso aleatorio continuo.
 

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Bibliography
BIBLIOGRAPHY

Scientific bibliography and references related to this product.

Vircell R&D Team. Evaluation of a new CLIA monotest assay for the detection of Helicobacter pylori antigen: a retrospective comparison with a Liaison® and SD Biosensor assays. Vircell internal evaluation; 2024 Feb; Granada, Spain. [Internal report/Abstrac
Viñuela L, et al. Estudio retrospectivo comparativo de un nuevo ensayo de CLIA para la detección de antígeno de Helicobacter pylori. In: Congreso SEIMC; 2024. Poster 0988.