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Human Cytomegalovirus Congenital (cCMV) Infection Following Primary and Nonprimary Maternal Infection: Perspectives of Prevention through Vaccine Development

机译:原发性和非原发性母亲感染后人巨细胞病毒先天性(cCMV)感染:通过疫苗开发的预防观点。

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摘要

Congenital cytomegalovirus (cCMV) might occur as a result of the human cytomegalovirus (HCMV) primary (PI) or nonprimary infection (NPI) in pregnant women. Immune correlates of protection against cCMV have been partly identified only for PI. Following either PI or NPI, HCMV strains undergo latency. From a diagnostic standpoint, while the serological criteria for the diagnosis of PI are well-established, those for the diagnosis of NPI are still incomplete. Thus far, a recombinant gB subunit vaccine has provided the best results in terms of partial protection. This partial efficacy was hypothetically attributed to the post-fusion instead of the pre-fusion conformation of the gB present in the vaccine. Future efforts should be addressed to verify whether a new recombinant gB pre-fusion vaccine would provide better results in terms of prevention of both PI and NPI. It is still a matter of debate whether human hyperimmune globulin are able to protect from HCMV vertical transmission. In conclusion, the development of an HCMV vaccine that would prevent a significant portion of PI would be a major step forward in the development of a vaccine for both PI and NPI.
机译:孕妇中的人巨细胞病毒(HCMV)原发性(PI)或非原发性感染(NPI)可能会导致先天性巨细胞病毒(cCMV)。仅针对PI已经部分鉴定了针对cCMV的免疫相关保护。在PI或NPI之后,HCMV菌株会出现潜伏期。从诊断的角度来看,虽然已经确立了诊断PI的血清学标准,但诊断NPI的血清学标准仍不完善。迄今为止,就部分保护而言,重组gB亚单位疫苗已提供了最佳结果。假设该部分功效归因于疫苗中存在的gB的融合后构象,而不是融合前构象。应该进一步努力验证新的重组gB融合前疫苗在预防PI和NPI方面是否能提供更好的结果。人类超免疫球蛋白是否能够防止HCMV垂直传播仍然是一个争论的问题。总之,开发可预防大部分PI的HCMV疫苗将是PI和NPI疫苗开发的重要一步。

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