α1proteinase inhibitor regulates cd4+ lymphocyte levels and is rate limiting in hiv-1 diseaseα1proteinase抑制剂调节cd4 +淋巴细胞水平和速度限制在hiv - 1的疾病.pdfVIP
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α1proteinaseinhibitorregulatescd4lymphocytelevelsandisratelimitinginhiv-1diseaseα1proteinase抑制剂调节cd4淋巴细胞水平和速度限制在hiv-1的疾病
a Proteinase Inhibitor Regulates CD4+ Lymphocyte 1 Levels and Is Rate Limiting in HIV-1 Disease 1,2 1,2 3 4 2 Cynthia L. Bristow *, Mariya A. Babayeva , Michelle LaBrunda , Michael P. Mullen , Ronald Winston 1 Weill Cornell Medical College, New York, New York, United States of America, 2 Institute for Human Genetics and Biochemistry, Vesenaz, Switzerland, 3 Holmes Regional Medical Center, Melbourne, Florida, United States of America, 4 Mount Sinai School of Medicine, New York, New York, United States of America Abstract Background: The regulation of adult stem cell migration through human hematopoietic tissue involves the chemokine CXCL12 (SDF-1) and its receptor CXCR4 (CD184). In addition, human leukocyte elastase (HLE) plays a key role. When HLE is located on the cell surface (HLE ), it acts not as a proteinase, but as a receptor for a proteinase inhibitor (a PI, a antitrypsin, CS 1 1 1 SerpinA1). Binding of a PI to HLE forms a motogenic complex. We previously demonstrated that a PI deficiency attends 1 CS 1 HIV-1 disease and that a1PI augmentation produces increased numbers of immunocompetent circulating CD4+ lymphocytes. Herein we investigated the mechanism underlying the a PI deficiency that attends HIV-1 infection.
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