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Tetrameric glycoprotein complex gH/gL/gQ1/gQ2 is a promising vaccine candidate for human herpesvirus 6B

Primary infection of human herpesvirus 6B (HHV-6B) occurs in infants after the decline of maternal immunity and causes exanthema subitum accompanied by a high fever, and it occasionally develops into encephalitis resulting in neurological sequelae. There is no effective prophylaxis for HHV-6B, and i...

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Detalles Bibliográficos
Autores principales: Wang, Bochao, Hara, Kouichi, Kawabata, Akiko, Nishimura, Mitsuhiro, Wakata, Aika, Tjan, Lidya Handayani, Poetranto, Anna Lystia, Yamamoto, Chisato, Haseda, Yasunari, Aoshi, Taiki, Munakata, Lisa, Suzuki, Ryo, Komatsu, Masato, Tsukamoto, Ryuko, Itoh, Tomoo, Nishigori, Chikako, Saito, Yasuyuki, Matozaki, Takashi, Mori, Yasuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377363/
https://www.ncbi.nlm.nih.gov/pubmed/32702057
http://dx.doi.org/10.1371/journal.ppat.1008609
Descripción
Sumario:Primary infection of human herpesvirus 6B (HHV-6B) occurs in infants after the decline of maternal immunity and causes exanthema subitum accompanied by a high fever, and it occasionally develops into encephalitis resulting in neurological sequelae. There is no effective prophylaxis for HHV-6B, and its development is urgently needed. The glycoprotein complex gH/gL/gQ1/gQ2 (called 'tetramer of HHV-6B') on the virion surface is a viral ligand for its cellular receptor human CD134, and their interaction is thus essential for virus entry into the cells. Herein we examined the potency of the tetramer as a vaccine candidate against HHV-6B. We designed a soluble form of the tetramer by replacing the transmembrane domain of gH with a cleavable tag, and the tetramer was expressed by a mammalian cell expression system. The expressed recombinant tetramer is capable of binding to hCD134. The tetramer was purified to homogeneity and then administered to mice with aluminum hydrogel adjuvant and/or CpG oligodeoxynucleotide adjuvant. After several immunizations, humoral and cellular immunity for HHV-6B was induced in the mice. These results suggest that the tetramer together with an adjuvant could be a promising candidate HHV-6B vaccine.