Protection from Bacterial Infection by a Single Vaccination with Replication-Deficient Mutant Herpes Simplex Virus Type 1

التفاصيل البيبلوغرافية
العنوان: Protection from Bacterial Infection by a Single Vaccination with Replication-Deficient Mutant Herpes Simplex Virus Type 1
المؤلفون: Kristen M. Kerksiek, Dirk H. Busch, Penelope Mavromara, Roberto Manservigi, Peggy Marconi, Aleksandra Bozac, Henning Lauterbach, Alberto L. Epstein, Thomas Brocker, Elena Berto
المصدر: Journal of Virology. 78:4020-4028
بيانات النشر: American Society for Microbiology, 2004.
سنة النشر: 2004
مصطلحات موضوعية: CD4-Positive T-Lymphocytes, Immunology, Mice, Transgenic, Herpesvirus 1, Human, CD8-Positive T-Lymphocytes, Biology, Virus Replication, Major histocompatibility complex, Microbiology, DNA vaccination, Mice, Immune system, Virology, Vaccines and Antiviral Agents, Animals, Cytotoxic T cell, Listeriosis, Vaccines, Synthetic, Intracellular parasite, Viral Vaccines, Bacterial Infections, Vaccination, Bacterial vaccine, Insect Science, Mutation, biology.protein, CD8, T-Lymphocytes, Cytotoxic
الوصف: Adaptive immune responses in which CD8+T cells recognize pathogen-derived peptides in the context of major histocompatibility complex class I molecules play a major role in the host defense against infection with intracellular pathogens. Cells infected with intracellular bacteria such asListeria monocytogenes,Salmonella entericaserovar Typhimurium, orMycobacterium tuberculosisare directly lysed by cytotoxic CD8+T cells. For this reason, current vaccines for intracellular pathogens, such as subunit vaccines or viable bacterial vaccines, aim to generate robust cytotoxic T-cell responses. In order to investigate the capacity of a herpes simplex virus type 1 (HSV-1) vector to induce strong cytotoxic effector cell responses and protection from infection with intracellular pathogens, we developed a replication-deficient, recombinant HSV-1 (rHSV-1) vaccine. We demonstrate in side-by-side comparison with DNA vaccination that rHSV-1 vaccination induces very strong CD8+effector T-cell responses. While both vaccines provided protection from infection withL. monocytogenesat low, but lethal doses, only rHSV-1 vaccines could protect from higher infectious doses; HSV-1 induced potent memory cytotoxic T lymphocytes that, upon challenge by pathogens, efficiently protected the animals. Despite the stimulation of relatively low humoral and CD4-T-cell responses, rHSV-1 vectors are strong candidates for future vaccine strategies that confer efficient protection from subsequent infection with intracellular bacteria.
تدمد: 1098-5514
0022-538X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c94b4cc1755dce7ad51533ea683e7296Test
https://doi.org/10.1128/jvi.78.8.4020-4028.2004Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....c94b4cc1755dce7ad51533ea683e7296
قاعدة البيانات: OpenAIRE