Correlation between CD4+ T-cell loss and Gag-specific T cells in different intestinal sites of chronically SIV-infected rhesus monkeys
Autor: | Christiane Stahl-Hennig, Tina Schultheiss |
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Rok vydání: | 2011 |
Předmět: |
CD4-Positive T-Lymphocytes
Male Immunology Simian Acquired Immunodeficiency Syndrome Uterus Gene Products gag Ileum Virus Replication medicine.disease_cause Immune system medicine Animals Immunology and Allergy Cytotoxic T cell Intestinal Mucosa biology T lymphocyte Simian immunodeficiency virus biology.organism_classification Macaca mulatta Rhesus macaque CTL Infectious Diseases medicine.anatomical_structure Female T-Lymphocytes Cytotoxic |
Zdroj: | AIDS. 25:429-433 |
ISSN: | 0269-9370 |
Popis: | Objective: To determine the loss of CD4 + T cells and virus-specific cytotoxic T cells (CTL) in different mucosal sites of rhesus monkeys infected with simian immunodeficiency virus (SIV). Design: A cross-sectional comparative investigation of seven different mucosal sites from chronically SIV-infected rhesus monkeys was performed by analyzing blood and mucosal lymphocytes. Methods: Mucosal lymphocytes were isolated from duodenum, jejunum, ileum and colon as well as from vagina, cervix and uterus of SIV-infected rhesus monkeys at necropsy. CD4 + T cells and SIV-Gag-specific CTL were determined in blood and mucosal samples by flow cytometry. Results: A significant depletion of CD4 + T cells was observed in blood and all mucosal sites of SIV-infected rhesus monkeys compared to uninfected animals. But the mean percentage loss of CD4 + T cells varied between 66 and 95% between the different mucosal tissues. The frequency of CTL ranged between 0.4 and 2.4% with the highest proportions in vagina and cervix. Among the intestinal sites the mean levels of CTL correlated with mean percentage loss of CD4 + T cells. Conclusion: A discriminative pronounced loss of CD4 + T cells among the mucosal tissues confirmed that viral replication affects different mucosal sites in a distinct way. Despite high levels of CTL, especially in vagina and cervix, the severe loss of mucosal CD4 + T cells could not be prevented during chronic SIV infection. However, within the four sites of the intestine a high virus-specific cellular immune response correlated with better preservation of CD4 + T cells. |
Databáze: | OpenAIRE |
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