Inflammation, immunity, and vaccines for Helicobacter

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Inflammation, immunity, and vaccines for Helicobacter. / Aebischer, Toni; Meyer, Thomas F; Andersen, Leif P.

In: Helicobacter (Oxford), Vol. 15 Suppl 1, 01.09.2010, p. 21-8.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Aebischer, T, Meyer, TF & Andersen, LP 2010, 'Inflammation, immunity, and vaccines for Helicobacter', Helicobacter (Oxford), vol. 15 Suppl 1, pp. 21-8. https://doi.org/10.1111/j.1523-5378.2010.00777.x

APA

Aebischer, T., Meyer, T. F., & Andersen, L. P. (2010). Inflammation, immunity, and vaccines for Helicobacter. Helicobacter (Oxford), 15 Suppl 1, 21-8. https://doi.org/10.1111/j.1523-5378.2010.00777.x

Vancouver

Aebischer T, Meyer TF, Andersen LP. Inflammation, immunity, and vaccines for Helicobacter. Helicobacter (Oxford). 2010 Sep 1;15 Suppl 1:21-8. https://doi.org/10.1111/j.1523-5378.2010.00777.x

Author

Aebischer, Toni ; Meyer, Thomas F ; Andersen, Leif P. / Inflammation, immunity, and vaccines for Helicobacter. In: Helicobacter (Oxford). 2010 ; Vol. 15 Suppl 1. pp. 21-8.

Bibtex

@article{5f2ec6c7d00445fca033b604900af8f2,
title = "Inflammation, immunity, and vaccines for Helicobacter",
abstract = "Helicobacter pylori represents the major etiologic agent of gastritis, gastric, and duodenal ulcer disease and can cause gastric cancer and mucosa-associated lymphoid tissue B-cell lymphoma. It is clear that the consequences of infection reflect diverse outcomes of the interaction of bacteria and host immune system. The hope is that by deciphering the deterministic rules--if any--of this interplay, we will eventually be able to predict, treat, and ultimately prevent disease. Over the past year, research on the immunology of this infection started to probe the role of small noncoding RNAs, a novel class of immune response regulators. Furthermore, we learned new details on how infection is detected by innate pattern recognition receptors. Induction of effective cell-mediated immunity will be key for the development of a vaccine, and new work published analyzed the relevance and contribution of CD4 T helper cell subsets to the immune reaction. Th17 cells, which are also induced during natural infection, were shown to be particularly important for vaccination. Cost-efficiency of vaccination was re-assessed and confirmed. Thus, induction and shaping of the effector roles of such protective Th populations will be a target of the newly described vaccine antigens, formulations, and modes of application that we also review here.",
keywords = "Bacterial Vaccines, CD4-Positive T-Lymphocytes, Helicobacter Infections, Helicobacter pylori, Humans, Inflammation, Th17 Cells",
author = "Toni Aebischer and Meyer, {Thomas F} and Andersen, {Leif P}",
note = "{\textcopyright} 2010 Blackwell Publishing Ltd.",
year = "2010",
month = sep,
day = "1",
doi = "10.1111/j.1523-5378.2010.00777.x",
language = "English",
volume = "15 Suppl 1",
pages = "21--8",
journal = "Helicobacter",
issn = "1083-4389",
publisher = "Wiley-Blackwell",

}

RIS

TY - JOUR

T1 - Inflammation, immunity, and vaccines for Helicobacter

AU - Aebischer, Toni

AU - Meyer, Thomas F

AU - Andersen, Leif P

N1 - © 2010 Blackwell Publishing Ltd.

PY - 2010/9/1

Y1 - 2010/9/1

N2 - Helicobacter pylori represents the major etiologic agent of gastritis, gastric, and duodenal ulcer disease and can cause gastric cancer and mucosa-associated lymphoid tissue B-cell lymphoma. It is clear that the consequences of infection reflect diverse outcomes of the interaction of bacteria and host immune system. The hope is that by deciphering the deterministic rules--if any--of this interplay, we will eventually be able to predict, treat, and ultimately prevent disease. Over the past year, research on the immunology of this infection started to probe the role of small noncoding RNAs, a novel class of immune response regulators. Furthermore, we learned new details on how infection is detected by innate pattern recognition receptors. Induction of effective cell-mediated immunity will be key for the development of a vaccine, and new work published analyzed the relevance and contribution of CD4 T helper cell subsets to the immune reaction. Th17 cells, which are also induced during natural infection, were shown to be particularly important for vaccination. Cost-efficiency of vaccination was re-assessed and confirmed. Thus, induction and shaping of the effector roles of such protective Th populations will be a target of the newly described vaccine antigens, formulations, and modes of application that we also review here.

AB - Helicobacter pylori represents the major etiologic agent of gastritis, gastric, and duodenal ulcer disease and can cause gastric cancer and mucosa-associated lymphoid tissue B-cell lymphoma. It is clear that the consequences of infection reflect diverse outcomes of the interaction of bacteria and host immune system. The hope is that by deciphering the deterministic rules--if any--of this interplay, we will eventually be able to predict, treat, and ultimately prevent disease. Over the past year, research on the immunology of this infection started to probe the role of small noncoding RNAs, a novel class of immune response regulators. Furthermore, we learned new details on how infection is detected by innate pattern recognition receptors. Induction of effective cell-mediated immunity will be key for the development of a vaccine, and new work published analyzed the relevance and contribution of CD4 T helper cell subsets to the immune reaction. Th17 cells, which are also induced during natural infection, were shown to be particularly important for vaccination. Cost-efficiency of vaccination was re-assessed and confirmed. Thus, induction and shaping of the effector roles of such protective Th populations will be a target of the newly described vaccine antigens, formulations, and modes of application that we also review here.

KW - Bacterial Vaccines

KW - CD4-Positive T-Lymphocytes

KW - Helicobacter Infections

KW - Helicobacter pylori

KW - Humans

KW - Inflammation

KW - Th17 Cells

U2 - 10.1111/j.1523-5378.2010.00777.x

DO - 10.1111/j.1523-5378.2010.00777.x

M3 - Journal article

C2 - 21054649

VL - 15 Suppl 1

SP - 21

EP - 28

JO - Helicobacter

JF - Helicobacter

SN - 1083-4389

ER -

ID: 34251507