ARNAX is an ideal adjuvant for COVID-19 vaccines to enhance antigen-specific CD4+ and CD8+ T-cell responses and neutralizing antibody induction

被引:1
作者
Kawakita, Tomomi [1 ,2 ,3 ]
Sekiya, Toshiki [2 ,3 ,4 ,5 ]
Kameda, Yayoi [6 ]
Nomura, Naoki [3 ,7 ]
Ohno, Marumi [2 ,3 ,8 ]
Handabile, Chimuka [2 ,3 ]
Yamaya, Akari [9 ]
Fukuhara, Hideo [2 ,10 ]
Anraku, Yuki [11 ,12 ]
Kita, Shunsuke [2 ,11 ,12 ]
Toba, Shinsuke [13 ,14 ]
Tsukamoto, Hirotake [15 ]
Sawa, Tomohiro [16 ]
Oshiumi, Hiroyuki [17 ]
Itoh, Yasushi [18 ]
Maenaka, Katsumi [2 ,10 ,11 ,12 ,19 ]
Sato, Akihiko [2 ,13 ,14 ]
Sawa, Hirofumi [2 ,4 ,8 ,14 ]
Suzuki, Yasuhiko [2 ,6 ]
Brown, Lorena E. [4 ,5 ]
Jackson, David C. [4 ,5 ]
Kida, Hiroshi [1 ,2 ,3 ,4 ]
Matsumoto, Misako [1 ,9 ,20 ]
Seya, Tsukasa [1 ,9 ,20 ]
Shingai, Masashi [1 ,2 ,3 ,4 ]
机构
[1] Hokkaido Univ, Int Inst Zoonosis Control, Div Vaccine Immunol, Sapporo, Japan
[2] Hokkaido Univ, Inst Vaccine Res & Dev HU IVReD, Sapporo, Japan
[3] Hokkaido Univ, Int Inst Zoonosis Control, Div Biol Dev, Sapporo, Japan
[4] Hokkaido Univ, Int Inst Zoonosis Control, Int Collaborat Unit, Sapporo, Japan
[5] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Australia
[6] Hokkaido Univ, Int Inst Zoonosis Control, Div Bioresources, Sapporo, Japan
[7] Hokkaido Univ, Int Inst Zoonosis Control, Div Int Res Promot, Sapporo, Japan
[8] Hokkaido Univ, One Hlth Res Ctr, Sapporo, Japan
[9] Aomori Univ, Nebuta Res Inst Life Sci, Aomori, Japan
[10] Hokkaido Univ, Int Inst Zoonosis Control, Div Pathogen Struct, Sapporo, Japan
[11] Hokkaido Univ, Lab Biomol Sci, Sapporo, Japan
[12] Hokkaido Univ, Fac Pharmaceut Sci, Ctr Res & Educ Drug Discovery, Sapporo, Japan
[13] Shionogi & Co Ltd, Shionogi Pharmaceut Res Ctr, Toyonaka, Japan
[14] Hokkaido Univ, Int Inst Zoonosis Control, Div Mol Pathobiol, Sapporo, Japan
[15] Kyoto Univ, Ctr Canc Immunotherapy & Immunobiol, Grad Sch Med, Div Clin Immunol & Canc Immunotherapy, Kyoto, Japan
[16] Kumamoto Univ, Grad Sch Med Sci, Dept Microbiol, Kumamoto, Japan
[17] Kumamoto Univ, Fac Life Sci, Grad Sch Med Sci, Dept Immunol, Kumamoto, Japan
[18] Shiga Univ Med Sci, Dept Pathol, Div Pathogenesis & Dis Regulat, Otsu, Japan
[19] Hokkaido Univ, Global Stn Biosurfaces & Drug Discovery, Sapporo, Japan
[20] Hokkaido Univ, Grad Sch Med, Dept Vaccine Immunol, Sapporo, Japan
关键词
ARNAX; TLR3; adjuvant; COVID-19; TOLL-LIKE RECEPTORS; POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID; CRYO-EM STRUCTURE; POLY-L-LYSINE; DENDRITIC CELLS; INTERFERON-BETA; ALUMINUM ADJUVANTS; CANCER; EXPRESSION; CYTOKINE;
D O I
10.1128/jvi.02290-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
ARNAX is a synthetic nucleotide-based Toll-like receptor 3 (TLR3) ligand that specifically stimulates the TLR3/TIR domain-containing adaptor molecule 1 (TICAM-1) pathway without activating inflammatory responses. ARNAX activates cellular immunity via cross-presentation; hence, its practical application has been demonstrated in cancer immunotherapy. Given the importance of cellular immunity in virus infections, ARNAX is expected to be a more effective vaccine adjuvant for virus infections than alum, an adjuvant approved for human use that mainly enhances humoral immunity. In the present study, the trimeric recombinant spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was prepared as a vaccine antigen and formulated with ARNAX. When T-cell and neutralizing antibody responses were evaluated in immunized mice, antigen formulated with ARNAX generated significantly larger numbers of antigenspecific CD4+ and CD8+ T cells, as well as higher titers of neutralizing antibodies, compared to antigen alone or antigen formulated with alum. In experiments where immunized mice were challenged with a SARS-CoV-2 mouse-adapted virus derived from the ancestral strain, immunization with antigen formulated with ARNAX reduced virus titers in the lungs at 3 days post-infection to a much greater extent than did immunization with either antigen alone or that formulated with alum. These results show that ARNAX potently enhances the levels of both cellular and humoral immunity above those seen with alum, providing significantly greater viral clearing responses. Thus, ARNAX may act as a useful adjuvant for prophylactic vaccines, particularly for viral infectious diseases.IMPORTANCECellular immunity is a critical immunological defense system against virus infections. However, aluminum salts, the most widely used adjuvant for vaccines for human use, do not promote strong cellular immunity. To prepare for the next pandemic of viral origin, the development of Th1-type adjuvants with low adverse reactions that induce cellular immunity is necessary. ARNAX is a TLR3 agonist consisting of DNA-RNA hybrid nucleic acid, which is expected to be an adjuvant that induces cellular immunity. The present study using a coronavirus disease 2019 mouse model demonstrated that ARNAX potently induces cellular immunity in addition to humoral immunity with minimal induction of inflammatory cytokines. Therefore, ARNAX has the potential to be used as a potent and welltolerated adjuvant for vaccines against pandemic viruses emerging in the future.
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页数:24
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共 76 条
[11]   Cross-protective immunity following coronavirus vaccination and coronavirus infection [J].
Dangi, Tanushree ;
Palacio, Nicole ;
Sanchez, Sarah ;
Park, Mincheol ;
Class, Jacob ;
Visvabharathy, Lavanya ;
Ciucci, Thomas ;
Koralnik, Igor J. ;
Richner, Justin M. ;
Penaloza-MacMaster, Pablo .
JOURNAL OF CLINICAL INVESTIGATION, 2021, 131 (24)
[12]   Aluminium adjuvants in vaccines-A way to modulate the immune response [J].
Danielsson, Ravi ;
Eriksson, Hakan .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2021, 115 :3-9
[13]   IgG Anti-Spike Antibodies and Surrogate Neutralizing Antibody Levels Decline Faster 3 to 10 Months After BNT162b2 Vaccination Than After SARS-CoV-2 Infection in Healthcare Workers [J].
Decru, Bram ;
Van Elslande, Jan ;
Steels, Sophie ;
Van Pottelbergh, Gijs ;
Godderis, Lode ;
Van Holm, Bram ;
Bossuyt, Xavier ;
Van Weyenbergh, Johan ;
Maes, Piet ;
Vermeersch, Pieter .
FRONTIERS IN IMMUNOLOGY, 2022, 13
[14]   The Nlrp3 inflammasome is critical for aluminium hydroxide-mediated IL-1β secretion but dispensable for adjuvant activity [J].
Franchi, Luigi ;
Nunez, Gabriel .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2008, 38 (08) :2085-2089
[15]   Essential role of mda-5 in type IIFN responses to polyriboinosinic: polyribocytidylic acid and encephalomyocarditis picornavirus [J].
Gitlin, Leonid ;
Barchet, Winfried ;
Gilfillan, Susan ;
Cella, Marina ;
Beutler, Bruce ;
Flavell, Richard A. ;
Diamond, Michael S. ;
Colonna, Marco .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (22) :8459-8464
[16]   TLR3 is essential for the induction of protective immunity against Punta Toro virus infection by the double-stranded RNA (dsRNA), poly(I:C12U), but not poly(I:C):: Differential, recognition of synthetic dsRNA molecules [J].
Gowen, Brian B. ;
Wong, Min-Hui ;
Jung, Kie-Hoon ;
Sanders, Andrew B. ;
Mitchell, William M. ;
Alexopoulou, Lena ;
Flavell, Richard A. ;
Sidwell, Robert W. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (08) :5200-5208
[17]   Human influenza viruses and CD8+ T cell responses [J].
Grant, Emma J. ;
Quinones-Parra, Sergio M. ;
Clemens, E. Bridie ;
Kedzierska, Katherine .
CURRENT OPINION IN VIROLOGY, 2016, 16 :132-142
[18]   Neuromodulation by a cytokine:: Interferon-β differentially augments neocortical neuronal activity and excitability [J].
Hadjilambreva, G ;
Mix, E ;
Rolfs, A ;
Müller, J ;
Strauss, U .
JOURNAL OF NEUROPHYSIOLOGY, 2005, 93 (02) :843-852
[19]   Central control of fever and female body temperature by RANKL/RANK [J].
Hanada, Reiko ;
Leibbrandt, Andreas ;
Hanada, Toshikatsu ;
Kitaoka, Shiho ;
Furuyashiki, Tomoyuki ;
Fujihara, Hiroaki ;
Trichereau, Jean ;
Paolino, Magdalena ;
Qadri, Fatimunnisa ;
Plehm, Ralph ;
Klaere, Steffen ;
Komnenovic, Vukoslav ;
Mimata, Hiromitsu ;
Yoshimatsu, Hironobu ;
Takahashi, Naoyuki ;
von Haeseler, Arndt ;
Bader, Michael ;
Kilic, Sara Sebnem ;
Ueta, Yoichi ;
Pifl, Christian ;
Narumiya, Shuh ;
Penninger, Josef M. .
NATURE, 2009, 462 (7272) :505-509
[20]   Fever, Immunity, and Molecular Adaptations [J].
Hasday, Jeffrey D. ;
Thompson, Christopher ;
Singh, Ishwar S. .
COMPREHENSIVE PHYSIOLOGY, 2014, 4 (01) :109-148