Boosting of post‐exposure human T‐cell and B‐cell recall responses in vivo by Burkholderia pseudomallei‐related proteins. Issue 1 (9th February 2017)

• Record Type: Journal Article
• Authors: Nithichanon, Arnone; Gourlay, Louise J.; Bancroft, Gregory J.; Ato, Manabu; Takahashi, Yoshimasa; Lertmemongkolchai, Ganjana
• Is Part Of: Immunology. Volume 151:Issue 1(2017)
• Page Start: 98
• Page End: 109
• Publication Date: 2017-02-09
• Subjects: antibodies -- B cell -- memory -- neutrophil -- T cell; Immunology -- Periodicals
• DOI: 10.1111/imm.12709
• Languages: English
• ISSNs: 0019-2805

Abstract

Summary: Burkholderia pseudomallei is the causative agent of melioidosis, an infectious disease with high incidence and mortality in South East Asia and northern Australia. To date there is no protective vaccine and antibiotic treatment is prolonged and not always effective. Most people living in endemic areas have been exposed to the bacteria and have developed some immunity, which may have helped to prevent disease. Here, we used a humanized mouse model (hu‐PBL‐SCID), reconstituted with human peripheral blood mononuclear cells from seropositive donors, to illustrate the potential of three known antigens (FliC, OmpA and N‐PilO2) for boosting both T‐cell and B‐cell immune responses. All three antigens boosted the production of specific antibodies in vivo, and increased the number of antibody and interferon‐ γ ‐secreting cells, and induced antibody affinity maturation. Moreover, antigen‐specific antibodies isolated from either seropositive individuals or boosted mice, were found to enhance phagocytosis and oxidative burst activities from human polymorphonuclear cells. Our study demonstrates that FliC, OmpA and N‐PilO2 can stimulate human memory T and B cells and highlight the potential of the hu‐PBL‐SCID system for screening and evaluation of novel protein antigens for inclusion in future vaccine trials against melioidosis. Abstract : Summary of the humanized mouse model (hu‐PBL‐SCID) reconstituted with human peripheral blood mononuclear cells from B. pseudomallei ‐seropositive donors, to illustrate the potential of three known antigens (FliC, OmpA and N‐PilO2) for boosting both T‐ and B‐cell immune responses.