Ministry of Scientific Research and Innovation
Institute of medical research and medicinal plant studies
Dr Nono Komguep is presently a research Officer & founder/head of the Unit of Immunobiology and Helminth Infections within the Institute of Medical research and Medicinal Plant studies of the Ministry of Scientific Research and Innovation of Cameroon . His work and that of his team (https://www.ibhi-lab.com/) revolve around the immunobiology of schistosomes, investigating how these parasites modulate the host immune response and how specific the changes driven by such parasites in the human host are and their potential as bases for the development of novel diagnostic, monitoring, prevention or treatment tools. He primarily engages in the teaching and training of BSc, MSc, MD, PharmD and PhD fellows in Cameroon & South Africa as an active mean to contribute to the achievement of ownership of research endeavours on local disease problems in Africa. Dr Nono is co-chair of the Global Schistosomiasis Alliance, Associate Editor for Plos Neglected Tropical Diseases, Invited Editor for Frontiers in Tropical Diseases, expert Reviewer for the European Union and Consultative expert for WHO/ESPEN.

Presenter of 1 Presentation

02. Parasites of humans

SCHISTOSOMIASIS INDUCES PLASMA B CELL DEATH IN THE BONE MARROW AND ACCELERATES THE DECLINE OVER TIME OF HOST VACCINE RESPONSES (ID 1888)

Session Type
02. Parasites of humans
Date
08/22/2022
Session Time
13:15 - 14:45
Room
Hall B4.M5+6
Lecture Time
13:35 - 13:55
Onsite or Pre-Recorded
Onsite

Abstract

Abstract Body

Schistosomiasis is a debilitating parasitic disease that is most common in Sub-Saharan Africa. The disease has previously been shown to influence systemic immunity towards unrelated antigens such as vaccines. However, mechanisms behind the parasite’s impact on vaccine mounted long-term immunity are not fully understood. We investigated the impact of chronic Schistosoma mansoni infection on the efficacy of vaccine-induced immunity in school-aged Cameroonian children and laboratory mice. Our findings highlighted impaired maintenance of long-term anti-polio vaccine-specific serological immunity in both vaccinated children and mice. Using a mouse model of anti-viral vaccination, additional mechanistic evaluations demonstrated that chronic schistosomiasis caused vaccine-elicited immunity impairment through reduced survival of plasmablasts and antibody-producing plasma B cells in the bone marrow. Treatment with praziquantel partially reversed the impact of chronic schistosomiasis on serological immunity of both vaccinated children and mice, and plasma B cell populations in the bone marrow of mice. Our results, therefore, demonstrate the morbid impact and a potential mechanism thereof, of chronic schistosomiasis on immunological responses induced by anti-viral vaccination. Further, this study presents praziquantel treatment as a potential strategic tool to improve vaccination effectiveness through ameliorated sustainability post-vaccination in at-risk population groups in schistosomiasis endemic regions. These findings are timely for the informed rollout of antiviral COVID-19 vaccines in Schistosomiasis-infested countries.

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