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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Pertussis Toxin Improves Immune Responses to a Combined Pneumococcal Antigen and Leads to Enhanced Protection against Streptococcus pneumoniae

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Author(s):
Salcedo-Rivillas, Carolina [1] ; Debrie, Anne-Sophie [2, 3, 4, 5] ; Miyaji, Eliane Namie [1] ; Ferreira, Jr., Jorge M. C. [6] ; Raw, Isaias [1] ; Locht, Camille [2, 3, 4, 5] ; Ho, Paulo L. [1, 7] ; Mielcarek, Nathalie [2, 3, 4, 5] ; Oliveira, Maria Leonor S. [1]
Total Authors: 9
Affiliation:
[1] Inst Butantan, Ctr Biotecnol, Sao Paulo - Brazil
[2] Inst Pasteur, Ctr Infect & Immun Lille, Lille - France
[3] INSERM, U1019, F-59045 Lille - France
[4] Inst Pasteur, Ctr Immunol & Biol Parasitaire, CNRS, UMR8204, F-59019 Lille - France
[5] Univ Lille Nord France, Lille - France
[6] Inst Butantan, Lab Imunoquim, Sao Paulo - Brazil
[7] Inst Butantan, Div Desenvolvimento Ind & Prod, Sao Paulo - Brazil
Total Affiliations: 7
Document type: Journal article
Source: Clinical and Vaccine Immunology; v. 21, n. 7, p. 972-981, JUL 2014.
Web of Science Citations: 1
Abstract

Pneumococcal surface protein A (PspA) is a candidate antigen for the composition of protein-based vaccines against Streptococcus pneumoniae. While searching for efficient adjuvants for PspA-based vaccines, our group has described the potential of combining PspA with the whole-cell pertussis vaccine (wP). When given to mice through the nasal route, a formulation composed of PspA from clade 5 (PspA5) and wP (PspA5-wP) induced high levels of antibodies and protection against challenges with different pneumococcal strains. PspA5-wP also induced the secretion of interleukin 17 (IL-17) by splenocytes and the infiltration of leukocytes in the lungs after challenge. Here, we show that protection against a pneumococcal invasive challenge was completely abrogated in mu MT-/- mice, which are deficient in the maturation of B cells, illustrating the importance of antibodies in the survival elicited by the PspA5-wP vaccine. Moreover, passive immunization showed that IgG purified from the sera of mice immunized with PspA5-wP conferred significant protection to naive mice, whereas the respective F(ab')(2) did not. Additionally, in vivo depletion of complement abolished protection against the pneumococcal challenge. The combination of PspA5 with wild-type or mutant Bordetella pertussis strains or with purified components showed that the pertussis toxin (PT)-containing formulations induced the highest levels of antibodies and protection. This suggests that the adjuvant activity of wP in the PspA5 model is mediated at least in part by PT. The sera from mice immunized with such formulations displayed high IgG binding and induction of complement deposition on the pneumococcal surface in vitro, which is consistent with the in vivo results. (AU)

FAPESP's process: 11/24019-7 - Molecular basis of the adjuvant properties of Bordetella pertussis in combination with Streptococcus pneumoniae protein antigens
Grantee:Maria Leonor Sarno de Oliveira
Support Opportunities: Regular Research Grants