Kinetics of the Immune Response Profile in Guinea Pigs after Vaccination withMycobacterium bovisBCG and Infection withMycobacterium tuberculosis
العنوان: | Kinetics of the Immune Response Profile in Guinea Pigs after Vaccination withMycobacterium bovisBCG and Infection withMycobacterium tuberculosis |
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المؤلفون: | Jennifer L. Taylor, Ajay Grover, Andrew Keyser, Kimberly Arnett, Linda Izzo, JoLynn Troudt, Angelo Izzo, Drew A. Rholl |
المصدر: | Infection and Immunity. 77:4837-4846 |
بيانات النشر: | American Society for Microbiology, 2009. |
سنة النشر: | 2009 |
مصطلحات موضوعية: | Tuberculosis, T-Lymphocytes, medicine.medical_treatment, Guinea Pigs, Immunology, Microbiology, Mycobacterium tuberculosis, Immune system, Immunity, medicine, Animals, Host Response and Inflammation, Mycobacterium bovis, biology, Reverse Transcriptase Polymerase Chain Reaction, Flow Cytometry, medicine.disease, biology.organism_classification, Vaccination, Infectious Diseases, Cytokine, BCG Vaccine, Cytokines, Female, Parasitology, CD8 |
الوصف: | The guinea pig model of tuberculosis is used extensively in assessing novel vaccines, sinceMycobacterium bovisBCG vaccination effectively prolongs survival after low-dose aerosol infection with virulentM. tuberculosis. To better understand how BCG extends time to death after pulmonary infection withM. tuberculosis, we examined cytokine responses postvaccination and recruitment of activated T cells and cytokine response postinfection. At 10 weeks postvaccination, splenic gamma interferon (IFN-γ) mRNA was significantly elevated compared to the levels at 5 weeks in ex vivo stimulation assays. At 15, 40, 60, and 120 days postinfection, T-cell activation (CD4+CD62Llowand CD8+CD62Llow) and mRNA expression of IFN-γ, tumor necrosis factor alpha (TNF-α), interleukin-1 (IL-1), IL-10, IL-12, and eomesodermin were assessed. Our data show that at day 40, BCG-vaccinated guinea pigs had significantly increased levels of IFN-γ mRNA expression but decreased TNF-α mRNA expression in their lungs compared to the levels in nonvaccinated animals. At day 120, a time when nonvaccinated guinea pigs succumbed to infection, low levels of IFN-γ mRNA were observed even though there were increasing levels of IL-1, IL-12, and IL-10, and the numbers of activated T cells did not differ from those in BCG-vaccinated animals. BCG vaccination conferred the advantage of recruiting greater numbers of CD4+CD62LlowT cells at day 40, although the numbers of CD8+CD62LlowT cells were not elevated compared to the numbers in nonvaccinated animals. Our data suggest that day 40 postinfection may be a pivotal time point in determining vaccine efficacy and prolonged survival and that BCG promotes the capacity of T cells in the lungs to respond to infection. |
تدمد: | 1098-5522 0019-9567 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d776bd232b2fb5c2b37fd45c90ba279 https://doi.org/10.1128/iai.00704-09 |
حقوق: | OPEN |
رقم الأكسشن: | edsair.doi.dedup.....1d776bd232b2fb5c2b37fd45c90ba279 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 10985522 00199567 |
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