Toxic Shock Syndrome: Characterization of Human Immune Responses to TSST-1 and Evidence for Sensitivity Thresholds
Noninvasive vaginal infections by Staphylococcus aureus strains producing the superantigen TSST-1 can cause menstrual toxic shock syndrome (mTSS). With the objective of exploring the basis for differential susceptibility to mTSS, the relative responsiveness to TSST-1 of healthy women has been invest...
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Published in | Toxicological sciences Vol. 134; no. 1; pp. 49 - 63 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.07.2013
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Online Access | Get full text |
ISSN | 1096-6080 1096-0929 1096-0929 |
DOI | 10.1093/toxsci/kft099 |
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Abstract | Noninvasive vaginal infections by Staphylococcus aureus strains producing the superantigen TSST-1 can cause menstrual toxic shock syndrome (mTSS). With the objective of exploring the basis for differential susceptibility to mTSS, the relative responsiveness to TSST-1 of healthy women has been investigated. Peripheral blood mononuclear cells from healthy donors were incubated with purified TSST-1 or with the T-cell mitogen phytohemmaglutinin (PHA), and proliferation was measured. The concentrations of TSST-1 and PHA required to elicit a response equivalent to 15% of the maximal achievable response (EC15) were determined. Although with PHA, EC15 values were comparable between donors, subjects could be classified as being of high, medium, or low sensitivity based on responsiveness to TSST-1. Sensitivity to TSST-1-induced proliferation was associated with increased production of the cytokines interleukin-2 and interferon-γ. When the entire T lymphocyte population was considered, there were no differences between sensitivity groups with respect to the frequency of cells known to be responsive to TSST-1 (those bearing CD3(+) Vβ2(+)). However, there was an association between sensitivity to TSST-1 and certain HLA-class II haplotypes. Thus, the frequencies of DR7DQ2, DR14DQ5, DR4DQ8, and DR8DQ4 haplotypes were greater among those with high sensitivity, a finding confirmed by analysis of responses to immortalized homozygous B cell lines. Collectively, the results reveal that factors other than neutralizing antibody and the frequency of Vβ2(+) T lymphocytes determine immunological responsiveness to TSST-1. Differential responsiveness of lymphocytes to TSST-1 may form the basis of interindividual variations in susceptibility to mTSS. |
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AbstractList | Noninvasive vaginal infections by Staphylococcus aureus strains producing the superantigen TSST-1 can cause menstrual toxic shock syndrome (mTSS). With the objective of exploring the basis for differential susceptibility to mTSS, the relative responsiveness to TSST-1 of healthy women has been investigated. Peripheral blood mononuclear cells from healthy donors were incubated with purified TSST-1 or with the T-cell mitogen phytohemmaglutinin (PHA), and proliferation was measured. The concentrations of TSST-1 and PHA required to elicit a response equivalent to 15% of the maximal achievable response (EC15) were determined. Although with PHA, EC15 values were comparable between donors, subjects could be classified as being of high, medium, or low sensitivity based on responsiveness to TSST-1. Sensitivity to TSST-1-induced proliferation was associated with increased production of the cytokines interleukin-2 and interferon-γ. When the entire T lymphocyte population was considered, there were no differences between sensitivity groups with respect to the frequency of cells known to be responsive to TSST-1 (those bearing CD3(+) Vβ2(+)). However, there was an association between sensitivity to TSST-1 and certain HLA-class II haplotypes. Thus, the frequencies of DR7DQ2, DR14DQ5, DR4DQ8, and DR8DQ4 haplotypes were greater among those with high sensitivity, a finding confirmed by analysis of responses to immortalized homozygous B cell lines. Collectively, the results reveal that factors other than neutralizing antibody and the frequency of Vβ2(+) T lymphocytes determine immunological responsiveness to TSST-1. Differential responsiveness of lymphocytes to TSST-1 may form the basis of interindividual variations in susceptibility to mTSS.Noninvasive vaginal infections by Staphylococcus aureus strains producing the superantigen TSST-1 can cause menstrual toxic shock syndrome (mTSS). With the objective of exploring the basis for differential susceptibility to mTSS, the relative responsiveness to TSST-1 of healthy women has been investigated. Peripheral blood mononuclear cells from healthy donors were incubated with purified TSST-1 or with the T-cell mitogen phytohemmaglutinin (PHA), and proliferation was measured. The concentrations of TSST-1 and PHA required to elicit a response equivalent to 15% of the maximal achievable response (EC15) were determined. Although with PHA, EC15 values were comparable between donors, subjects could be classified as being of high, medium, or low sensitivity based on responsiveness to TSST-1. Sensitivity to TSST-1-induced proliferation was associated with increased production of the cytokines interleukin-2 and interferon-γ. When the entire T lymphocyte population was considered, there were no differences between sensitivity groups with respect to the frequency of cells known to be responsive to TSST-1 (those bearing CD3(+) Vβ2(+)). However, there was an association between sensitivity to TSST-1 and certain HLA-class II haplotypes. Thus, the frequencies of DR7DQ2, DR14DQ5, DR4DQ8, and DR8DQ4 haplotypes were greater among those with high sensitivity, a finding confirmed by analysis of responses to immortalized homozygous B cell lines. Collectively, the results reveal that factors other than neutralizing antibody and the frequency of Vβ2(+) T lymphocytes determine immunological responsiveness to TSST-1. Differential responsiveness of lymphocytes to TSST-1 may form the basis of interindividual variations in susceptibility to mTSS. Noninvasive vaginal infections by Staphylococcus aureus strains producing the superantigen TSST-1 can cause menstrual toxic shock syndrome (mTSS). With the objective of exploring the basis for differential susceptibility to mTSS, the relative responsiveness to TSST-1 of healthy women has been investigated. Peripheral blood mononuclear cells from healthy donors were incubated with purified TSST-1 or with the T-cell mitogen phytohemmaglutinin (PHA), and proliferation was measured. The concentrations of TSST-1 and PHA required to elicit a response equivalent to 15% of the maximal achievable response (EC15) were determined. Although with PHA, EC15 values were comparable between donors, subjects could be classified as being of high, medium, or low sensitivity based on responsiveness to TSST-1. Sensitivity to TSST-1-induced proliferation was associated with increased production of the cytokines interleukin-2 and interferon-γ. When the entire T lymphocyte population was considered, there were no differences between sensitivity groups with respect to the frequency of cells known to be responsive to TSST-1 (those bearing CD3(+) Vβ2(+)). However, there was an association between sensitivity to TSST-1 and certain HLA-class II haplotypes. Thus, the frequencies of DR7DQ2, DR14DQ5, DR4DQ8, and DR8DQ4 haplotypes were greater among those with high sensitivity, a finding confirmed by analysis of responses to immortalized homozygous B cell lines. Collectively, the results reveal that factors other than neutralizing antibody and the frequency of Vβ2(+) T lymphocytes determine immunological responsiveness to TSST-1. Differential responsiveness of lymphocytes to TSST-1 may form the basis of interindividual variations in susceptibility to mTSS. |
Author | Modern, Paul Goering, Richard V. Tucker, Heidi Kimber, Ian Foertsch, Leslie M. Parsonnet, Jeffrey Donnellen, Meghan Gerberick, G. Frank Dearman, Rebecca J. Davis, Catherine C. Nookala, Suba Kotb, Malak Morel, Jorge |
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Cites_doi | 10.1093/infdis/147.4.783 10.1073/pnas.86.22.8941 10.1038/nm1431 10.1093/infdis/145.4.431 10.1080/00365540310015962 10.1111/j.1574-695X.2011.00808.x 10.1126/science.2185544 10.1128/JCM.00228-08 10.1016/S0002-9378(03)00873-1 10.1002/jps.21077 10.1007/s10875-007-9072-4 10.1186/1471-2334-10-249 10.1038/nm1202-800 10.3201/eid0903.020360 10.1073/pnas.88.1.125 10.1146/annurev.micro.55.1.77 10.4049/jimmunol.178.5.3076 10.4049/jimmunol.1002057 10.1056/NEJM198012183032501 10.1093/infdis/143.4.509 10.1016/0092-8674(89)90980-X 10.1128/JCM.22.1.26-31.1985 10.1128/JCM.37.10.3411-3414.1999 10.1074/jbc.M605544200 10.4049/jimmunol.175.10.6870 10.1128/JCM.43.9.4628-4634.2005 |
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SubjectTerms | Adolescent Adult Antibodies, Bacterial - blood B-Lymphocytes - drug effects B-Lymphocytes - immunology Bacterial Toxins - immunology Bacterial Toxins - toxicity Cell Proliferation - drug effects Cells, Cultured Cohort Studies Differential Threshold Dose-Response Relationship, Immunologic Enterotoxins - immunology Enterotoxins - toxicity Female Haplotypes HLA-D Antigens - genetics HLA-D Antigens - immunology Humans Interferon-gamma - biosynthesis Interferon-gamma - immunology Interleukin-2 - biosynthesis Interleukin-2 - immunology Leukocytes, Mononuclear - drug effects Leukocytes, Mononuclear - immunology Menstruation Mitogens - immunology Mitogens - pharmacology Phytohemagglutinins - immunology Phytohemagglutinins - pharmacology Shock, Septic - immunology Shock, Septic - microbiology Staphylococcal Infections - immunology Staphylococcal Infections - microbiology Staphylococcus aureus - immunology Staphylococcus aureus - isolation & purification Superantigens - immunology Superantigens - toxicity T-Lymphocytes - drug effects T-Lymphocytes - immunology Young Adult |
Title | Toxic Shock Syndrome: Characterization of Human Immune Responses to TSST-1 and Evidence for Sensitivity Thresholds |
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