Baden Lindsey R, Liu Jinyan, Li Hualin, Johnson Jennifer A, Walsh Stephen R, Kleinjan Jane A, Engelson Brian A, Peter Lauren, Abbink Peter, Milner Danny A, Golden Kevin L, Viani Kyle L, Stachler Matthew D, Chen Benjamin J, Pau Maria G, Weijtens Mo, Carey Brittany R, Miller Caroline A, Swann Edith M, Wolff Mark, Loblein Hayley, Seaman Michael S, Dolin Raphael, Barouch Dan H
Brigham and Women's Hospital Beth Israel Deaconess Medical Center Harvard Medical School Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard, Boston.
Beth Israel Deaconess Medical Center Harvard Medical School.
J Infect Dis. 2015 Feb 15;211(4):518-28. doi: 10.1093/infdis/jiu485. Epub 2014 Aug 26.
Defining mucosal immune responses and inflammation to candidate human immunodeficiency virus type 1 (HIV-1) vaccines represents a current research priority for the HIV-1 vaccine field. In particular, it is unclear whether intramuscular immunization can elicit immune responses at mucosal surfaces in humans.
In this double-blind, randomized, placebo-controlled clinical trial, we evaluated systemic and mucosal immune responses to a candidate adenovirus serotype 26 (Ad26) vectored HIV-1 envelop (Env) vaccine in baseline Ad26-seronegative and Ad26-seropositive healthy volunteers. Systematic mucosal sampling with rectal Weck-Cel sponges and rectal biopsies were performed.
Intramuscular immunization elicited both systemic and mucosal Env-specific humoral and cellular immune responses in the majority of subjects. Individuals with preexisting Ad26-specific neutralizing antibodies had vaccine-elicited immune responses comparable to those of subjects who were Ad26 seronegative. We also observed no increase in activated total or vector-specific mucosal CD4+ T lymphocytes following vaccination by either histopathology or flow cytometry.
These data demonstrate that a single intramuscular administration of this Ad26-vectored HIV-1 Env vaccine elicited both systemic and mucosal immune responses in humans. Induction of antigen-specific humoral and cellular mucosal immunity was not accompanied by a detectable increase in mucosal inflammation.
NCT01103687.
确定针对候选1型人类免疫缺陷病毒(HIV-1)疫苗的黏膜免疫反应和炎症是HIV-1疫苗领域当前的研究重点。特别是,肌肉注射免疫能否在人体黏膜表面引发免疫反应尚不清楚。
在这项双盲、随机、安慰剂对照临床试验中,我们评估了基线时Ad26血清阴性和Ad26血清阳性的健康志愿者对候选26型腺病毒(Ad26)载体HIV-1包膜(Env)疫苗的全身和黏膜免疫反应。使用直肠Weck-Cel海绵进行系统的黏膜采样并进行直肠活检。
肌肉注射免疫在大多数受试者中引发了全身和黏膜Env特异性体液和细胞免疫反应。预先存在Ad26特异性中和抗体的个体,其疫苗引发的免疫反应与Ad26血清阴性的受试者相当。通过组织病理学或流式细胞术,我们还观察到接种疫苗后活化的总黏膜或载体特异性CD4+T淋巴细胞没有增加。
这些数据表明,单次肌肉注射这种Ad26载体HIV-1 Env疫苗可在人体引发全身和黏膜免疫反应。抗原特异性体液和细胞黏膜免疫的诱导并未伴随着黏膜炎症的可检测增加。
NCT01103687。