A therapeutic HIV-1 vaccine enhances anti-HIV-1 immune responses in patients under highly active antiretroviral therapy

被引:21
|
作者
Tung, Frank Y. [1 ]
Tung, Jack K. [1 ]
Pallikkuth, Suresh [2 ]
Pahwa, Savita [2 ]
Fischl, Margaret A. [2 ]
机构
[1] GeneCure Biotechnol, 3150 Corners North Court, Peachtree Corners, GA USA
[2] Univ Miami, Sch Med, Miami, FL USA
关键词
HIV-1; Vaccine; Therapeutic vaccine; Immune responses; Viral load; Analytical treatment interruption; HUMAN-IMMUNODEFICIENCY-VIRUS; IMMUNIZATION; CELLS; TRIAL;
D O I
10.1016/j.vaccine.2016.03.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: HIV-1 specific cellular immunity plays an important role in controlling viral replication. In this first-in-human therapeutic vaccination study, a replication-defective HIV-1 vaccine (HIVAX) was tested in HIV-1 infected participants undergoing highly active antiretroviral therapy (HAART) to enhance anti-HIV immunity (Clinicaltrials.gov, identifier NCT01428596). Methods: A010 was a randomized, placebo-controlled trial to evaluate the safety and the immunogenicity of a replication defective HIV-1 vaccine (HIVAX) given as a subcutaneous injection to HIV-1 infected participants who were receiving HAART with HIV-1 viral load <50 copies/ml and CD4 cell count >500 cells/mm(3). HIV-1 specific immune responses were monitored by INF-gamma enzyme linked immunospot (Elispot) and intracellular cytokine staining (ICS) assay after vaccination. Following the randomized placebo-controlled vaccination phase, subjects who received HIVAX vaccine and who met eligibility underwent a 12-week analytical antiretroviral treatment interruption (ATI). Viral load was monitored throughout the study. Results: HIVAX was well tolerated in trial participants. Transient grade 1 to 2 (mild to moderate) injection site reactions occurred in 8 of 10 vaccinated participants. HIVAX was immunogenic in all vaccinated participants. The functionality of T cells was significantly enhanced after vaccination. Median viral load (3.45 log(10) copies/ml, range of 96-12,830 copies/m1) at the end of the 12-week treatment interruption in HIVAX vaccinated group was significantly lower than the pre-treatment levels. Three vaccinated participants extended ATI for up to 2 years with stable CD4 cells and low viral loads. Conclusions: HIVAX vaccine is generally safe, elicits strong anti-HIV-1 immune responses, and may play an important role in controlling viral load during treatment interruption in HIV-1 infected participants. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2225 / 2232
页数:8
相关论文
共 50 条
  • [31] T cell immune responses to HIV-1
    Vasan, Sandhya
    Schlesinger, Sarah J.
    Arrode, Geraldine
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2007, 12 : 2330 - 2343
  • [32] Phenotypic patterns of HIV-1 clonal populations during highly active antiretroviral therapy (HAART)
    Favia, A
    Di Stefano, M
    Fiore, JR
    Pastore, G
    Angarano, G
    MICROBIOLOGICA, 1999, 22 (04): : 301 - 307
  • [33] The Effect of a Year of Highly Active Antiretroviral Therapy on Immune Reconstruction and Cytokines in HIV/AIDS Patients
    Yao, Yunhai
    Luo, Yan
    He, Yan
    Zheng, Yuhuang
    Zhang, Quan
    Zhou, Huaying
    Zeng, Si
    Chen, Zi
    He, Bo
    He, Mei
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2013, 29 (04) : 691 - 697
  • [34] Anti-HIV-1 ADCC and HIV-1 Env Can Be Partners in Reducing Latent HIV Reservoir
    Suryawanshi, Poonam
    Bagul, Rajani
    Shete, Ashwini
    Thakar, Madhuri
    FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [35] Origins of a Vaccine-Induced, Human Anti-HIV-1 Antibody
    Julien, Jean-Philippe
    EBIOMEDICINE, 2015, 2 (07): : 632 - +
  • [36] Differences in serum IgA responses to HIV-1 gp41 in elite controllers compared to viral suppressors on highly active antiretroviral therapy
    Nabi, Rafiq
    Moldoveanu, Zina
    Wei, Qing
    Golub, Elizabeth T.
    Durkin, Helen G.
    Greenblatt, Ruth M.
    Herold, Betsy C.
    Nowicki, Marek J.
    Kassaye, Seble
    Cho, Michael W.
    Pinter, Abraham
    Landay, Alan L.
    Mestecky, Jiri
    Kozlowski, Pamela A.
    PLOS ONE, 2017, 12 (07):
  • [37] Early Combination Antiretroviral Therapy Limits HIV-1 Persistence in Children
    Luzuriaga, Katherine
    ANNUAL REVIEW OF MEDICINE, VOL 67, 2016, 67 : 201 - 213
  • [38] HIV-1 DNA vaccine with adjuvant cytokines induces specific immune responses against HIV-1 infection in mice
    Wang Fu-xiang
    Sun Yong-tao
    Wang Lin-xu
    Liu Juan
    CHINESE MEDICAL JOURNAL, 2006, 119 (12) : 1034 - 1037
  • [39] Immune responses of a designed HIV-1 DNA vaccine on rhesus monkeys
    ZHANG Lishu1
    2. College of Agricultural and Biological Engineer
    3. Laboratory Animal Center
    4. College of Life Science
    5. Agricultural Sciences Center
    Chinese Science Bulletin, 2006, (13) : 1571 - 1577