Pneumococcal serotype specific antibodies
Immunology
Sample and container requirements
Serum, EDTA plasma Li hep Plasma
Minimum volume required
4 ml Blood
Special requirements
None
Patient preparation
None
Sample viability
Store at 4oC prior to sending to referral lab
Turnaround time
14 days from receipt at referral laboratory
Reference range
>0.35 ug/mL for each individual serotype
Clinical guidance
Antibodies to 13 pneumococcal specific serotypes are measured. This test is used in the diagnosis of Primary Immune deficiency. This test should be requested for patients who have clincial history of recurrent infections and/or evidence of bronchiectasis. 11/13 serotypes tested are contained in the childhood conjugated pneumococcal vaccine Prevenar13 (introduced in 2010). Protective levels of these show satisfactory response to the T cell dependent antibody production pathway. All 13 serotypes are contained in the unconjugated vaccine Pneumovax. Protective response to Pneumovax infers normal funcioning of the T-independent antibody production pathway. Patients should have this test done in the following clinical circumstances: a) Patients, especially children, with recurrent bacterial sepsis; particularly of the upper and lower respiratory tract. b) Patients with invasive disease caused by encapsulated organisms.c) Patients with selective antibody deficiency states d) To assess Immunological reconstitution following Bone Marrow Transplant.e) Patients with haemoglobinopathies or who have had a splenectomy should have their levels of antibodies to encapsulated bacteria (i.e. pneumoccocal & Hib) monitored.
Notes
Samples referred to Addenbrookes http://www.baspath.co.uk/clinical_chemistry/guidelines/Addenbrookes%20Immunology%20Handbook%20v14.pdf
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This information was last updated on 17 August 2026