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BpOmpW Antigen Stimulates the Necessary Protective T-Cell Responses Against Melioidosis.

Authors :
Tomás-Cortázar, Julen
Bossi, Lorenzo
Quinn, Conor
Reynolds, Catherine J.
Butler, David K.
Corcoran, Niamh
Murchú, Maitiú Ó
McMahon, Eve
Singh, Mahavir
Rongkard, Patpong
Anguita, Juan
Blanco, Alfonso
Dunachie, Susanna J.
Altmann, Daniel
Boyton, Rosemary J.
Arnold, Johan
Giltaire, Severine
McClean, Siobhán
Source :
Frontiers in Immunology; 12/13/2021, Vol. 12, p1-13, 13p
Publication Year :
2021

Abstract

Melioidosis is a potentially fatal bacterial disease caused by Burkholderia pseudomallei and is estimated to cause 89,000 deaths per year in endemic areas of Southeast Asia and Northern Australia. People with diabetes mellitus are most at risk of melioidosis, with a 12-fold increased susceptibility for severe disease. Interferon gamma (IFN-γ) responses from CD4 and CD8 T cells, but also from natural killer (NK) and natural killer T (NKT) cells, are necessary to eliminate the pathogen. We previously reported that immunization with B. pseudomallei OmpW (BpOmpW antigen) protected mice from lethal B. pseudomallei challenge for up to 81 days. Elucidating the immune correlates of protection of the protective BpOmpW vaccine is an essential step prior to clinical trials. Thus, we immunized either non-insulin-resistant C57BL/6J mice or an insulin-resistant C57BL/6J mouse model of type 2 diabetes (T2D) with a single dose of BpOmpW. BpOmpW induced strong antibody responses, stimulated effector CD4<superscript>+</superscript> and CD8<superscript>+</superscript> T cells and CD4<superscript>+</superscript> CD25<superscript>+</superscript> Foxp3<superscript>+</superscript> regulatory T cells, and produced higher IFN-γ responses in CD4<superscript>+</superscript>, CD8<superscript>+</superscript>, NK, and NKT cells in non-insulin-resistant mice. The T-cell responses of insulin-resistant mice to BpOmpW were comparable to those of non-insulin-resistant mice. In addition, as a precursor to its evaluation in human studies, humanized HLA-DR and HLA-DQ (human leukocyte antigen DR and DQ isotypes, respectively) transgenic mice elicited IFN-γ recall responses in an enzyme-linked immune absorbent spot (ELISpot)-based study. Moreover, human donor peripheral blood mononuclear cells (PBMCs) exposed to BpOmpW for 7 days showed T-cell proliferation. Finally, plasma from melioidosis survivors with diabetes recognized our BpOmpW vaccine antigen. Overall, the range of approaches used strongly indicated that BpOmpW elicits the necessary immune responses to combat melioidosis and bring this vaccine closer to clinical trials. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16643224
Volume :
12
Database :
Complementary Index
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
154106777
Full Text :
https://doi.org/10.3389/fimmu.2021.767359