Frontiers in Immunology (Jun 2022)

Plasmablast Expansion Following the Tetravalent, Live-Attenuated Dengue Vaccine Butantan-DV in DENV-Naïve and DENV-Exposed Individuals in a Brazilian Cohort

  • Cássia G. T. Silveira,
  • Diogo M. Magnani,
  • Priscilla R. Costa,
  • Vivian I. Avelino-Silva,
  • Michael J. Ricciardi,
  • Maria do Carmo S. T. Timenetsky,
  • Raphaella Goulart,
  • Carolina A. Correia,
  • Mariana P. Marmorato,
  • Lilian Ferrari,
  • Zelinda B. Nakagawa,
  • Claudia Tomiyama,
  • Helena Tomiyama,
  • Jorge Kalil,
  • Ricardo Palacios,
  • Alexander R. Precioso,
  • Alexander R. Precioso,
  • David I. Watkins,
  • Esper G. Kallás,
  • Esper G. Kallás

DOI
https://doi.org/10.3389/fimmu.2022.908398
Journal volume & issue
Vol. 13

Abstract

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An effective vaccine against the dengue virus (DENV) should induce a balanced, long-lasting antibody (Ab) response against all four viral serotypes. The burst of plasmablasts in the peripheral blood after vaccination may reflect enriched vaccine-specific Ab secreting cells. Here we characterize the acute plasmablast responses from naïve and DENV-exposed individuals following immunization with the live attenuated tetravalent (LAT) Butantan DENV vaccine (Butantan-DV). The frequency of circulating plasmablasts was determined by flow cytometric analysis of fresh whole blood specimens collected from 40 participants enrolled in the Phase II Butantan-DV clinical trial (NCT01696422) before and after (days 6, 12, 15 and 22) vaccination. We observed a peak in the number of circulating plasmablast at day 15 after vaccination in both the DENV naïve and the DENV-exposed vaccinees. DENV-exposed vaccinees experienced a significantly higher plasmablast expansion. In the DENV-naïve vaccinees, plasmablasts persisted for approximately three weeks longer than among DENV-exposed volunteers. Our findings indicate that the Butantan-DV can induce plasmablast responses in both DENV-naïve and DENV-exposed individuals and demonstrate the influence of pre-existing DENV immunity on Butantan DV-induced B-cell responses.

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