Tetrameric glycoprotein complex gH/gL/gQ1/gQ2 is a promising vaccine candidate for human herpesvirus 6B.
Bochao WangKouichi HaraAkiko KawabataMitsuhiro NishimuraAika WakataLidya Handayani TjanAnna Lystia PoetrantoChisato YamamotoYasunari HasedaTaiki AoshiLisa MunakataRyo SuzukiMasato KomatsuRyuko TsukamotoTomoo ItohChikako NishigoriYasuyuki SaitoTakashi MatozakiYasuko MoriPublished in: PLoS pathogens (2020)
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.
Keyphrases
- endothelial cells
- early stage
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- pluripotent stem cells
- high glucose
- poor prognosis
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- drug delivery
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- adipose tissue
- gene expression
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- pregnant women
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- cell cycle arrest
- signaling pathway
- endoplasmic reticulum stress
- subarachnoid hemorrhage
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