Bhatt Urja, Herate Cecile, Estelien Reynette, Relouzat Francis, Dereuddre-Bosquet Nathalie, Maciorowski Dawid, Diop Cheikh, Couto Emma, Staiti Jillian, Cavarelli Mariangela, Bossevot Laëtitia, Sconosciuti Quentin, Bouchard Page, Le Grand Roger, Vandenberghe Luk H, Zabaleta Nerea
Grousbeck Gene Therapy Center, Ocular Genomics Institute and Schepens Eye Research Institute, Mass Eye and Ear, Boston, MA 02114, USA.
Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA.
Vaccines (Basel). 2024 Aug 2;12(8):882. doi: 10.3390/vaccines12080882.
PARVAX is a genetic vaccine platform based on an adeno-associated vector that has demonstrated to elicit potent, durable, and protective immunity in nonhuman primates (NHPs) after a single dose. Here, we assessed vaccine immunogenicity following a PARVAX prime-boost regimen against SARS-CoV-2. In mice, a low-dose prime followed by a higher-dose boost elicited potent neutralizing antibody responses and distinct cross-reactivity profiles, depending on the antigen used in the booster vaccine. However, the potent neutralizing anti-vector antibody responses developed in mice limited the dose that could be administered as a prime. We further explored the re-administration efficacy in NHPs primed with a SARS-CoV-2 Delta vaccine and boosted with an Omicron BA.1 vaccine at week 15, after the primary response peak antibody levels were reached. The boost elicited an increase in antibodies against several Omicron variants, but no increase was detected in the antibody titers for other variants. The anti-vector responses were low and showed some increased subsequent boosts but generally declined over time. The potent prime vaccination limited the detection of the boosting effect, and therefore, the effect of anti-vector immunity was not fully elucidated. These data show that PARVAX can be effectively re-administered and induce a novel antigenic response.
PARVAX是一种基于腺相关载体的基因疫苗平台,已证明单剂量给药后能在非人灵长类动物(NHP)中引发强效、持久和保护性免疫。在此,我们评估了PARVAX针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的初免-加强免疫方案后的疫苗免疫原性。在小鼠中,低剂量初免后给予高剂量加强免疫可引发强效中和抗体反应和不同的交叉反应谱,这取决于加强疫苗中使用的抗原。然而,小鼠体内产生的强效抗载体抗体反应限制了作为初免可给予的剂量。我们进一步探索了在15周时,在达到初次反应峰值抗体水平后,用SARS-CoV-2 Delta疫苗初免并用Omicron BA.1疫苗加强免疫的NHP中的再次给药效果。加强免疫引发了针对几种Omicron变体的抗体增加,但未检测到其他变体的抗体滴度增加。抗载体反应较低,后续加强免疫时有所增加,但总体上随时间下降。强效的初免疫苗接种限制了对加强免疫效果的检测,因此,抗载体免疫的效果尚未完全阐明。这些数据表明,PARVAX可以有效地再次给药并诱导新的抗原反应。