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
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