Academic Journal

Therapeutic Vaccination Expands and Improves the Function of the HIV-Specific Memory T-Cell Repertoire

التفاصيل البيبلوغرافية
العنوان: Therapeutic Vaccination Expands and Improves the Function of the HIV-Specific Memory T-Cell Repertoire
المؤلفون: Casazza, Joseph P., Bowman, Kathryn A., Adzaku, Selorm, Smith, Emily C., Enama, Mary E., Bailer, Robert T., Price, David A., Gostick, Emma, Gordon, Ingelise J., Ambrozak, David R., Nason, Martha C., Roederer, Mario, Andrews, Charla A., Maldarelli, Frank M., Wiegand, Ann, Kearney, Mary F., Persaud, Deborah, Ziemniak, Carrie, Gottardo, Raphael, Ledgerwood, Julie E., Graham, Barney S., Koup, Richard A., the VRC 101 Study Team, Holman, LaSonji, Hendel, Cynthia, Plummer, Sarah, Novik, Laura, Larkin, Brenda, Rucker, Steve, Costner, Pamela, Goswami, Trishna, Read, Sarah, Leitman, Susan, Decederfelt, Hope, Starling, Judith, Alley, Tiffany, Jones, Richard, Johnson, Diane, Jones, Sara, Sitar, Sandra, Stanford, LaChonne, Washington-Lewis, Rhonda, Thompson, Ericka, Rhone, Kathy, Zaia, Phyllis
بيانات النشر: Oxford University Press
سنة النشر: 2013
المجموعة: HighWire Press (Stanford University)
مصطلحات موضوعية: MAJOR ARTICLE
الوصف: Background. The licensing of herpes zoster vaccine has demonstrated that therapeutic vaccination can help control chronic viral infection. Unfortunately, human trials of immunodeficiency virus (HIV) vaccine have shown only marginal efficacy. Methods. In this double-blind study, 17 HIV-infected individuals with viral loads of <50 copies/mL and CD4+ T-cell counts of >350 cells/µL were randomly assigned to the vaccine or placebo arm. Vaccine recipients received 3 intramuscular injections of HIV DNA (4 mg) coding for clade B Gag, Pol, and Nef and clade A, B, and C Env, followed by a replication-deficient adenovirus type 5 boost (1010 particle units) encoding all DNA vaccine antigens except Nef. Humoral, total T-cell, and CD8+ cytotoxic T-lymphocyte (CTL) responses were studied before and after vaccination. Single-copy viral loads and frequencies of latently infected CD4+ T cells were determined. Results. Vaccination was safe and well tolerated. Significantly stronger HIV-specific T-cell responses against Gag, Pol, and Env, with increased polyfunctionality and a broadened epitope-specific CTL repertoire, were observed after vaccination. No changes in single-copy viral load or the frequency of latent infection were observed. Conclusions. Vaccination of individuals with existing HIV-specific immunity improved the magnitude, breadth, and polyfunctionality of HIV-specific memory T-cell responses but did not impact markers of viral control. Clinical Trials Registration. NCT00270465
نوع الوثيقة: text
وصف الملف: text/html
اللغة: English
Relation: http://jid.oxfordjournals.org/cgi/content/short/jit098v2; http://dx.doi.org/10.1093/infdis/jit098
DOI: 10.1093/infdis/jit098
الاتاحة: http://jid.oxfordjournals.org/cgi/content/short/jit098v2
https://doi.org/10.1093/infdis/jit098
Rights: Copyright (C) 2013, Infectious Diseases Society of America
رقم الانضمام: edsbas.DA21606E
قاعدة البيانات: BASE