Potent Plasmablast-Derived Antibodies Elicited by the National Institutes of Health Dengue Vaccine
| Autor: | Sebastian P. Fuchs, Diogo M. Magnani, Ronald C. Desrosiers, Maria do Carmo Sampaio Tavares Timenetsky, Priscilla R. Costa, Dennis R. Burton, Nuria Pedreño-Lopez, Martin J. Gutman, Michael J. Ricciardi, Aline Domingues, Jorge Kalil, Mauricio A. Martins, Cassia G. T. Silveira, Jens Wrammert, Helen S. Maxwell, Raphaella Goulart, Esper G. Kallas, José M. Martinez-Navio, David I. Watkins, Lucas Gonzalez-Nieto, Stephen S. Whitehead, Lilian Ferrari, Varian K. Bailey |
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| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Adult Male Immunology Population Plasma Cells Dengue Vaccines Biology Dengue virus medicine.disease_cause Antibodies Viral Microbiology Neutralization Dengue fever 03 medical and health sciences Immunity Virology Vaccines and Antiviral Agents medicine Humans education Dengue vaccine education.field_of_study Antibodies Monoclonal Dengue Virus medicine.disease Antibodies Neutralizing United States Vaccination 030104 developmental biology HEK293 Cells Immunization National Institutes of Health (U.S.) Insect Science Female |
| Popis: | Exposure to dengue virus (DENV) is thought to elicit lifelong immunity, mediated by DENV-neutralizing antibodies (nAbs). However, Abs generated by primary infections confer serotype-specific protection, and immunity against other serotypes develops only after subsequent infections. Accordingly, the induction of these nAb responses acquired after serial DENV infections has been a long-sought-after goal for vaccination. Nonetheless, it is still unclear if tetravalent vaccines can elicit or recall nAbs. In this study, we have characterized the responses from a volunteer who had been previously exposed to DENV and was immunized with the live attenuated tetravalent vaccine Butantan-DV, developed by the NIH and Butantan Institute. Eleven days after vaccination, we observed an ∼70-fold expansion of the plasmablast population. We generated 21 monoclonal Abs (MAbs) from singly sorted plasmablasts. These MAbs were the result of clonal expansions and had significant levels of somatic hypermutation (SHM). Nineteen MAbs (90.5%) neutralized at least one DENV serotype at concentrations of 1 μg/ml or less; 6 of the 21 MAbs neutralized three or more serotypes. Despite the tetravalent composition of the vaccine, we observed a neutralization bias in the induced repertoire: DENV3 was targeted by 18 of the 19 neutralizing MAbs (nMAbs). Furthermore, the P3D05 nMAb neutralized DENV3 with extraordinary potency (concentration to achieve half-maximal neutralization [Neut 50 ] = 0.03 μg/ml). Thus, the Butantan-DV vaccine engendered a mature, antigen-selected B cell repertoire. Our results suggest that preexisting responses elicited by a previous DENV3 infection were recalled by immunization. IMPORTANCE The dengue epidemic presents a global public health challenge that causes widespread economic burden and remains largely unchecked by existing control strategies. Successful control of the dengue epidemic will require effective prophylactic and therapeutic interventions. Several vaccine clinical efficacy trials are approaching completion, and the chances that one or more live attenuated tetravalent vaccines (LATVs) will be introduced worldwide is higher than ever. While it is widely accepted that dengue virus (DENV)-neutralizing antibody (nAb) titers are associated with protection, the Ab repertoire induced by LATVs remain uncharacterized. Here, we describe the isolation of potent (Neut 50 < 0.1 μg/ml) nAbs from a DENV-seropositive volunteer immunized with the tetravalent vaccine Butantan-DV, which is currently in phase III trials. |
| Databáze: | OpenAIRE |
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