Immunogenicity and efficacy of one and two doses of Ad26.COV2.S COVID vaccine in adult and aged NHP

Ad26.COV2.S COVID疫苗单剂和两剂在成年和老年非人灵长类动物中的免疫原性和有效性

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作者:Laura Solforosi # ,Harmjan Kuipers # ,Mandy Jongeneelen ,Sietske K Rosendahl Huber ,Joan E M van der Lubbe ,Liesbeth Dekking ,Dominika N Czapska-Casey ,Ana Izquierdo Gil ,Miranda R M Baert ,Joke Drijver ,Joost Vaneman ,Ella van Huizen ,Ying Choi ,Jessica Vreugdenhil ,Sanne Kroos ,Adriaan H de Wilde ,Eleni Kourkouta ,Jerome Custers ,Remko van der Vlugt ,Daniel Veldman ,Jeroen Huizingh ,Krisztian Kaszas ,Tim J Dalebout ,Sebenzile K Myeni ,Marjolein Kikkert ,Eric J Snijder ,Dan H Barouch ,Kinga P Böszörményi ,Marieke A Stammes ,Ivanela Kondova ,Ernst J Verschoor ,Babs E Verstrepen ,Gerrit Koopman ,Petra Mooij ,Willy M J M Bogers ,Marjolein van Heerden ,Leacky Muchene ,Jeroen T B M Tolboom ,Ramon Roozendaal ,Boerries Brandenburg ,Hanneke Schuitemaker ,Frank Wegmann ,Roland C Zahn

Abstract

Safe and effective coronavirus disease-19 (COVID-19) vaccines are urgently needed to control the ongoing pandemic. While single-dose vaccine regimens would provide multiple advantages, two doses may improve the magnitude and durability of immunity and protective efficacy. We assessed one- and two-dose regimens of the Ad26.COV2.S vaccine candidate in adult and aged nonhuman primates (NHPs). A two-dose Ad26.COV2.S regimen induced higher peak binding and neutralizing antibody responses compared with a single dose. In one-dose regimens, neutralizing antibody responses were stable for at least 14 wk, providing an early indication of durability. Ad26.COV2.S induced humoral immunity and T helper cell (Th cell) 1-skewed cellular responses in aged NHPs that were comparable to those in adult animals. Aged Ad26.COV2.S-vaccinated animals challenged 3 mo after dose 1 with a SARS-CoV-2 spike G614 variant showed near complete lower and substantial upper respiratory tract protection for both regimens. Neutralization of variants of concern by NHP sera was reduced for B.1.351 lineages while maintained for the B.1.1.7 lineage independent of Ad26.COV2.S vaccine regimen.

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