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Bordetella pertussis Antibodies, IgM

Code:17033

Synonyms
Антитела класса IgМ к возбудителю коклюшаантитела класса IgМ к Bordetella pertussisиммуноглобулины класса М к Bordetella pertussisАнтитела класса IgМ к бактерии Борде – Жангу.Anti-Bordetella pertussis IgMBordetella pertussis IgM antibodiesBordetella pertussis immunoglobulin MIgM antibodies to Bordet-Gengou bacillusPertussis IgM antibodies

Analysis details

Methodology

  • Enzyme-linked immunosorbent assay (ELISA)

Expected Turnaround Time

1–2 days

Special Instructions

  • Do not smoke for at least 30 minutes before the blood draw.

How to use

The Bordetella pertussis Antibodies, IgM assay (also referred to as Anti-Bordetella pertussis IgM or Pertussis IgM antibodies) assists in the serologic diagnosis of pertussis by identifying pathogen-specific IgM. It supports recognition of acute or ongoing infection beginning about the second week after symptoms start and has particular utility in unvaccinated children. This test is interpreted alongside clinical and epidemiologic information and is commonly paired with direct detection methods such as culture and PCR to confirm infection.

Limitations

Pertussis is a human respiratory illness caused by the aerobic, gram-negative coccobacillus Bordetella pertussis and spreads via respiratory droplets. The illness follows incubation, catarrhal, paroxysmal, and convalescent stages; the paroxysmal phase features spasmodic coughing, an inspiratory whoop, and vomiting after coughing. Leukocytosis with absolute lymphocytosis is frequently observed. Major antigens that elicit host antibody responses include pertussis toxin, filamentous hemagglutinin, pertactin, outer-membrane proteins, lipopolysaccharide, and agglutinogens. Humoral responses evolve over time: IgA and IgM usually emerge during the second week after symptom onset, while IgG reaches a peak around weeks 6–8 and then wanes. Finding elevated Bordetella pertussis–specific IgM, either alone or together with IgA and/or IgG, supports an acute or recent infection, particularly in persons without prior vaccination. Very early sampling or altered immune function may result in low IgM despite true infection. Serology serves as an adjunct to culture and PCR, and results require interpretation in the context of the clinical presentation and epidemiologic exposure.

Reference interval
MinMax
09
IndicationsClinical picture suggestive of pertussis, including paroxysmal cough with inspiratory whoop, posttussive vomiting, or cyanosis, often with normal or low-grade fever and lymphocytic leukocytosis, Workup of suspected Bordetella pertussis infection when testing occurs at or after 2 weeks from symptom onset, Evaluation of individuals with close exposure to a laboratory-confirmed pertussis case, Differential diagnosis of paroxysmal cough syndromes versus viral upper respiratory infection, measles, acute bronchitis, pneumonia, or asthma

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Storage InstructionsRefrigerated, Frozen

References

Ghanaie RM, Karimi A, Sadeghi H, Esteghamti A, Falah F, Armin S, Fahimzad A, Shamshiri A, Kahbazi M, Shiva F. Sensitivity and specificity of the World Health Organization pertussis clinical case definition. Int J Infect Dis. 2010 Dec;14(12):e1072-5.

Piekarska K, Rzeczkowska M, Rastawicki W, Dąbrowska-Iwanicka A, Paradowska-Stankiewicz I. Usefulness of laboratory methods in diagnosis of pertussis in adult with paroxysmal cough. Przegl Epidemiol. 2014;68(4):633-6.

Guiso N, Berbers G, Fry NK, He Q, Riffelmann M, Wirsing von König CH; EU Pertstrain group. What to do and what not to do in serological diagnosis of pertussis: recommendations from EU reference laboratories. Eur J Clin Microbiol Infect Dis. 2011 Mar;30(3):307-12.

Laboratory manual for the diagnosis of whooping cough caused by Bordetella pertussis and Bordetella parapertussis. World Health Organization. Dept. of Immunization, Vaccines and Biologicals. WHO/IVB/04.14, 2004.

Respiratory infections. Diagnosis of pertussis and parapertussis. Methodological guidelines MR 3.1.2.0072-13.