Joseph B. Margolick , Albert D. Donnenberg , Clara Chu , Maurice R.G. O'Gorman , Janis V. Giorgi , Alvaro Muñoz
{"title":"总T细胞计数下降与艾滋病发病有关,与CD4+淋巴细胞计数无关:对艾滋病发病机制的影响","authors":"Joseph B. Margolick , Albert D. Donnenberg , Clara Chu , Maurice R.G. O'Gorman , Janis V. Giorgi , Alvaro Muñoz","doi":"10.1006/clin.1998.4577","DOIUrl":null,"url":null,"abstract":"<div><p>We previously reported that blind T cell homeostasis, in which the total T cell count is maintained but the CD4<sup>+</sup>and CD8<sup>+</sup>subset composition of the T cells can vary, fails approximately 1.5 to 2.5 years before the onset of AIDS. The present study was premised on the hypothesis that if failure of T cell homeostasis (i.e., a decline in total T cell counts) is important in the pathogenesis of AIDS, it should be a significant predictor of AIDS after controlling for the CD4<sup>+</sup>lymphocyte count. Data from 1556 homosexual men with sufficient sequential T cell subset measurements were evaluated, representing 11,988 person-visits in men with known clinical outcomes over a period of more than 10 years. Using regression models that incorporated CD4<sup>+</sup>lymphocyte count and HIV-related symptoms (fever, thrush), it was determined that a yearly decline of more than 300 T cells/μl of peripheral blood was an independent predictor of the onset of AIDS for subjects with CD4<sup>+</sup>lymphocyte counts of <500 cells/μl. The results support an important role for failure of T cell homeostasis in the pathogenesis of AIDS.</p></div>","PeriodicalId":10683,"journal":{"name":"Clinical immunology and immunopathology","volume":"88 3","pages":"Pages 256-263"},"PeriodicalIF":0.0000,"publicationDate":"1998-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/clin.1998.4577","citationCount":"25","resultStr":"{\"title\":\"Decline in Total T Cell Count Is Associated with Onset of AIDS, Independent of CD4+Lymphocyte Count: Implications for AIDS Pathogenesis\",\"authors\":\"Joseph B. Margolick , Albert D. Donnenberg , Clara Chu , Maurice R.G. O'Gorman , Janis V. Giorgi , Alvaro Muñoz\",\"doi\":\"10.1006/clin.1998.4577\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We previously reported that blind T cell homeostasis, in which the total T cell count is maintained but the CD4<sup>+</sup>and CD8<sup>+</sup>subset composition of the T cells can vary, fails approximately 1.5 to 2.5 years before the onset of AIDS. The present study was premised on the hypothesis that if failure of T cell homeostasis (i.e., a decline in total T cell counts) is important in the pathogenesis of AIDS, it should be a significant predictor of AIDS after controlling for the CD4<sup>+</sup>lymphocyte count. Data from 1556 homosexual men with sufficient sequential T cell subset measurements were evaluated, representing 11,988 person-visits in men with known clinical outcomes over a period of more than 10 years. Using regression models that incorporated CD4<sup>+</sup>lymphocyte count and HIV-related symptoms (fever, thrush), it was determined that a yearly decline of more than 300 T cells/μl of peripheral blood was an independent predictor of the onset of AIDS for subjects with CD4<sup>+</sup>lymphocyte counts of <500 cells/μl. The results support an important role for failure of T cell homeostasis in the pathogenesis of AIDS.</p></div>\",\"PeriodicalId\":10683,\"journal\":{\"name\":\"Clinical immunology and immunopathology\",\"volume\":\"88 3\",\"pages\":\"Pages 256-263\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1006/clin.1998.4577\",\"citationCount\":\"25\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical immunology and immunopathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0090122998945779\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical immunology and immunopathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0090122998945779","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Decline in Total T Cell Count Is Associated with Onset of AIDS, Independent of CD4+Lymphocyte Count: Implications for AIDS Pathogenesis
We previously reported that blind T cell homeostasis, in which the total T cell count is maintained but the CD4+and CD8+subset composition of the T cells can vary, fails approximately 1.5 to 2.5 years before the onset of AIDS. The present study was premised on the hypothesis that if failure of T cell homeostasis (i.e., a decline in total T cell counts) is important in the pathogenesis of AIDS, it should be a significant predictor of AIDS after controlling for the CD4+lymphocyte count. Data from 1556 homosexual men with sufficient sequential T cell subset measurements were evaluated, representing 11,988 person-visits in men with known clinical outcomes over a period of more than 10 years. Using regression models that incorporated CD4+lymphocyte count and HIV-related symptoms (fever, thrush), it was determined that a yearly decline of more than 300 T cells/μl of peripheral blood was an independent predictor of the onset of AIDS for subjects with CD4+lymphocyte counts of <500 cells/μl. The results support an important role for failure of T cell homeostasis in the pathogenesis of AIDS.