Memory B cell responses induced by pneumococcal conjugate vaccine schedules with fewer doses: analysis of a randomised-controlled trial in Viet Nam

Author:

Ong Darren1ORCID,Thanh Phan Van2,Temple Beth3,Toh Zheng Quan1ORCID,Nguyen Cattram1ORCID,Vientrung Kien2,Nguyen Hoang Van Anh2,Dai  Vo Thi Trang2,Bright Kathryn4,Tran Hau Phuc2,Higgins Rachel4,Cheung Yin Bun5,Nguyen Thuong2,Mulholland Kim6,Licciardi Paul1ORCID

Affiliation:

1. Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia

2. Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam

3. Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia; Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia; Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom

4. Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia

5. Centre for Quantitative Medicine and Program in Health Services & Systems Research, Duke-NUS Medical School, Singapore; Tampere Center for Child, Adolescent and Maternal Health Research, Tampere University, Tampere, Finland

6. Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia; Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom

Abstract

Abstract

The use of pneumococcal conjugate vaccine (PCV) schedules with fewer doses are being considered to reduce costs and improve access, particularly in low- and middle-income countries. While several studies have assessed their immunogenicity, there are limited data on their potential for long-term immune protection, as assessed by pneumococcal serotype-specific memory B cell (Bmem) responses. This study aimed to compare Bmem responses following reduced-dose (0 + 1 and 1 + 1) schedules of PCV10 and PCV13 in Vietnamese infants from our randomised-controlled trial. Following vaccination at 12 months of age, Bmem levels for most serotypes peaked seven days post-vaccination and were higher in magnitude for the 1 + 1 than 0 + 1 schedules and for PCV13 than PCV10. Furthermore, Bmem did not wane as rapidly as IgG levels by 24 months of age. Further studies are needed to assess the use of Bmem as markers of long-term protection against pneumococcal carriage and disease, which is crucial to generate data for immunisation program decision-making.

Publisher

Springer Science and Business Media LLC

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