Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.

Salmonella enterica serovar Typhi (S. Typhi), the causative agent of the typhoid fever, is a pathogen of great public health importance. Typhoid vaccines have the potential to be cost-effective measures towards combating this disease, yet the antigens triggering host protective immune responses are...

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Main Authors: Rosângela Salerno-Gonçalves, Hervé Tettelin, David Lou, Stephanie Steiner, Tasmia Rezwanul, Qin Guo, William D Picking, Vishvanath Nene, Marcelo B Sztein
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-09-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0005912&type=printable
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author Rosângela Salerno-Gonçalves
Hervé Tettelin
David Lou
Stephanie Steiner
Tasmia Rezwanul
Qin Guo
William D Picking
Vishvanath Nene
Marcelo B Sztein
author_facet Rosângela Salerno-Gonçalves
Hervé Tettelin
David Lou
Stephanie Steiner
Tasmia Rezwanul
Qin Guo
William D Picking
Vishvanath Nene
Marcelo B Sztein
author_sort Rosângela Salerno-Gonçalves
collection DOAJ
description Salmonella enterica serovar Typhi (S. Typhi), the causative agent of the typhoid fever, is a pathogen of great public health importance. Typhoid vaccines have the potential to be cost-effective measures towards combating this disease, yet the antigens triggering host protective immune responses are largely unknown. Given the key role of cellular-mediated immunity in S. Typhi protection, it is crucial to identify S. Typhi proteins involved in T-cell responses. Here, cells from individuals immunized with Ty21a typhoid vaccine were collected before and after immunization and used as effectors. We also used an innovative antigen expressing system based on the infection of B-cells with recombinant Escherichia coli (E. coli) expressing one of four S. Typhi gene products (i.e., SifA, OmpC, FliC, GroEL) as targets. Using flow cytometry, we found that the pattern of response to specific S. Typhi proteins was variable. Some individuals responded to all four proteins while others responded to only one or two proteins. We next evaluated whether T-cells responding to recombinant E. coli also possess the ability to respond to purified proteins. We observed that CD4+ cell responses, but not CD8+ cell responses, to recombinant E. coli were significantly associated with the responses to purified proteins. Thus, our results demonstrate the feasibility of using an E. coli expressing system to uncover the antigen specificity of T-cells and highlight its applicability to vaccine studies. These results also emphasize the importance of selecting the stimuli appropriately when evaluating CD4+ and CD8+ cell responses.
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spelling doaj-art-912e6ffd1b154a7db1f7b073f966437a2025-08-20T02:45:30ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352017-09-01119e000591210.1371/journal.pntd.0005912Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.Rosângela Salerno-GonçalvesHervé TettelinDavid LouStephanie SteinerTasmia RezwanulQin GuoWilliam D PickingVishvanath NeneMarcelo B SzteinSalmonella enterica serovar Typhi (S. Typhi), the causative agent of the typhoid fever, is a pathogen of great public health importance. Typhoid vaccines have the potential to be cost-effective measures towards combating this disease, yet the antigens triggering host protective immune responses are largely unknown. Given the key role of cellular-mediated immunity in S. Typhi protection, it is crucial to identify S. Typhi proteins involved in T-cell responses. Here, cells from individuals immunized with Ty21a typhoid vaccine were collected before and after immunization and used as effectors. We also used an innovative antigen expressing system based on the infection of B-cells with recombinant Escherichia coli (E. coli) expressing one of four S. Typhi gene products (i.e., SifA, OmpC, FliC, GroEL) as targets. Using flow cytometry, we found that the pattern of response to specific S. Typhi proteins was variable. Some individuals responded to all four proteins while others responded to only one or two proteins. We next evaluated whether T-cells responding to recombinant E. coli also possess the ability to respond to purified proteins. We observed that CD4+ cell responses, but not CD8+ cell responses, to recombinant E. coli were significantly associated with the responses to purified proteins. Thus, our results demonstrate the feasibility of using an E. coli expressing system to uncover the antigen specificity of T-cells and highlight its applicability to vaccine studies. These results also emphasize the importance of selecting the stimuli appropriately when evaluating CD4+ and CD8+ cell responses.https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0005912&type=printable
spellingShingle Rosângela Salerno-Gonçalves
Hervé Tettelin
David Lou
Stephanie Steiner
Tasmia Rezwanul
Qin Guo
William D Picking
Vishvanath Nene
Marcelo B Sztein
Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.
PLoS Neglected Tropical Diseases
title Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.
title_full Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.
title_fullStr Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.
title_full_unstemmed Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.
title_short Use of a novel antigen expressing system to study the Salmonella enterica serovar Typhi protein recognition by T cells.
title_sort use of a novel antigen expressing system to study the salmonella enterica serovar typhi protein recognition by t cells
url https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0005912&type=printable
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