O-Specific Polysaccharide-Specific Memory B Cell Responses in Young Children, Older Children, and Adults Infected with Vibrio cholerae O1 Ogawa in Bangladesh

Author:

Aktar Amena1,Rahman M. Arifur1,Afrin Sadia1,Faruk M. Omar1,Uddin Taher1,Akter Aklima1,Sami M. Israk Nur1,Yasmin Tahirah1,Chowdhury Fahima1,Khan Ashraful I.1,Leung Daniel T.23,LaRocque Regina C.23,Charles Richelle C.23,Bhuiyan Taufiqur Rahman1,Mandlik Anjali2,Kelly Meagan2,Kováč Pavol4,Xu Peng4,Calderwood Stephen B.235,Harris Jason B.267,Qadri Firdausi1,Ryan Edward T.238

Affiliation:

1. International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh

2. Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA

3. Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA

4. NIDDK, LBC, National Institutes of Health, Bethesda, Maryland, USA

5. Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, USA

6. Division of Global Health, Massachusetts General Hospital for Children, Boston, Massachusetts, USA

7. Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA

8. Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts, USA

Abstract

ABSTRACT Cholera caused by Vibrio cholerae O1 confers at least 3 to 10 years of protection against subsequent disease regardless of age, despite a relatively rapid fall in antibody levels in peripheral blood, suggesting that memory B cell responses may play an important role in protection. The V. cholerae O1-specific polysaccharide (OSP) component of lipopolysaccharide (LPS) is responsible for serogroup specificity, and it is unclear if young children are capable of developing memory B cell responses against OSP, a T cell-independent antigen, following cholera. To address this, we assessed OSP-specific memory B cell responses in young children (2 to 5 years, n = 11), older children (6 to 17 years, n = 21), and adults (18 to 55 years, n = 28) with cholera caused by V. cholerae O1 in Dhaka, Bangladesh. We also assessed memory B cell responses against LPS and vibriocidal responses, and plasma antibody responses against OSP, LPS, and cholera toxin B subunit (CtxB; a T cell-dependent antigen) on days 2 and 7, as well as days 30, 90, and 180 after convalescence. In all age cohorts, vibriocidal responses and plasma OSP, LPS, and CtxB-specific responses peaked on day 7 and fell toward baseline over the follow-up period. In comparison, we were able to detect OSP memory B cell responses in all age cohorts of patients with detectable responses over baseline for 90 to 180 days. Our results suggest that OSP-specific memory B cell responses can occur following cholera, even in the youngest children, and may explain in part the age-independent induction of long-term immunity following naturally acquired disease.

Funder

HHS | National Institutes of Health

HHS | NIH | Fogarty International Center

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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