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Sudan ebolavirus long recovered survivors produce GP-specific Abs | 11412
Immunome Research

Immunome Research
Open Access

ISSN: 1745-7580

Sudan ebolavirus long recovered survivors produce GP-specific Abs that are of the IgG1 subclass and preferentially bind FcγRI


9th Molecular Immunology & Immunogenetics Congress

March 08-09, 2018 | London, UK

Olga Radinsky, Avishay Edri, Leslie Lobel and Angel Porgador

Ben Gurion University of the Negev, Israel

Posters & Accepted Abstracts: Immunome Res

Abstract :

Ebolavirus is a highly lethal pathogen, causing a severe hemorrhagic disease with a high fatality rate. To better understand immune correlates of protection by virus specific IgG, we investigated the evolution of the Fc�?³ receptors (Fc�?³Rs)-activating capabilities of antiviral IgG in serum samples of long recovered survivors. To this end, longitudinal serum samples from survivors of Sudan ebolavirus (SUDV) infection, studied over years, were examined for the presence of Ebola-GP specific IgG subclasses, and for their binding to Fc�?³Rs. We developed a cell-based reporter system to quantitate pathogen-specific antibody binding to Fc�?³RIIIA, Fc�?³RIIA, Fc�?³RIIB and Fc�?³RI. With this system, we demonstrate that anti-GP-specific stimulation of the Fc�?³RI reporter by survivorsâ�?�? sera was substantially high one year after acute infection, with a slight reduction in activity over a decade post infection. We further demonstrate that GP-specific IgG1 is by far the seroprevalent subclass that retained and even enhanced its presence in the sera, over ten years post infection; the prevalence of other GP-specific IgG subclasses was considerably reduced over time. In accordance, GP-specific Fc�?³RI reporter response and GP-specific total IgG1 subclass correlated in the studied group of Ebola survivors. These observations are important for further informing Ebola vaccine and therapeutic development. Recent Publications 1. Sobarzo A et al. (2013) Persistent immune responses after Ebola virus infection. N. Engl. J. Med. 369: 492-493. 2. Sobarzo A et al. (2013) Profile and persistence of the virus-specific neutralizing humoral immune response in human survivors of Sudan ebolavirus (Gulu). J. Infect. Dis. 208: 299-309. 3. Ackerman M E et al. (2013) Natural variation in Fc glycosylation of HIV-specific antibodies impacts antiviral activity. J. Clin. Invest. 123(5): 2183-2192. 4. Nelson E A et al. (2016) Clomiphene and its isomers block ebola virus particle entry and infection with similar potency: potential therapeutic implications. Viruses. 8(8). pii: E206. 5. Baize S et al. (2002) Inflammatory responses in ebola virus-infected patients. Clin. Exp. Immunol. 128(1): 163-168 (2002).

Biography :

Olga Radinsky is a PhD student under supervision of Professor Angel Porgador, doing her research in the Immunology field at Ben Gurion University of Negev in Israel. As a part of PhD studying, she developed cell-based reporter system based on the expression of CD3zeta-fused FcγRs in BW cells to quantitate total and pathogen-specific antibody binding to Fcγ-Receptors. Using this system, she completed analysis of sera from patients with different health conditions: Alzheimer patients, cancer patients, recurrent abortions in women, and long-recovered survivors of SUDV infection.
 Email:kisterev@post.bgu.ac.il

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