Antibody persistence 5 years after a 13-valent pneumococcal conjugate vaccine in asplenic patients with β-thalassemia: assessing the need for booster

Streptococcus pnemoniae is a major cause of morbidity and mortality among splenectomised patients with β -thalassemia major. We have previously shown that a 13-valent pneumococcal conjugate vaccine (PCV13) induces robust early immune responses in such patients, while history of repeated immunisation...

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Veröffentlicht in:Annals of hematology 2019-03, Vol.98 (3), p.775-779
Hauptverfasser: Papadatou, Ioanna, Lagousi, Theano, Kattamis, Antonis, Spoulou, Vana
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Sprache:eng
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Zusammenfassung:Streptococcus pnemoniae is a major cause of morbidity and mortality among splenectomised patients with β -thalassemia major. We have previously shown that a 13-valent pneumococcal conjugate vaccine (PCV13) induces robust early immune responses in such patients, while history of repeated immunisations with the 23-valent polysaccharide pneumococcal vaccine (PPSV23) results in attenuation of the response to PCV13. However, the duration of vaccine-induced protection in splenectomised thalassemic patients and the associated need for booster immunisation remains unclear. In the current study, we enumerate antibody persistence 5 years post-PCV13 and investigate any correlation with early immune response and immunisation history. Pneumococcal serotype (PS)-specific antibodies against 5 vaccine antigens were measured 5 years post-PCV13 in 34 asplenic adults with β- thalassemia. PS-specific antibodies against 5 vaccine serotypes had declined significantly at 5 years post-PCV13 (year 5).Year 5 antibody titres remained above baseline for PS9V, 19A and19F, returned to baseline for PS23F, and dropped below baseline for PS3 ( p  
ISSN:0939-5555
1432-0584
DOI:10.1007/s00277-019-03615-z