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Reproductive Cloning01:27

Reproductive Cloning

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Reproductive cloning is the process of producing a genetically identical copy—a clone—of an entire organism. While clones can be produced by splitting an early embryo—similar to what happens naturally with identical twins—cloning of adult animals is usually done by a process called somatic cell nuclear transfer (SCNT).
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic...
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Cloning of Dolly the Sheep01:08

Cloning of Dolly the Sheep

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The first successfully cloned mammal was Dolly, a sheep, born on 5th July 1996 at Roslin Institute, Scotland. The cloned sheep was named after the American singer Dolly Parton. Dolly lived for seven years and died of respiratory complications, which is speculated to be due to the actual age of her DNA. Because the DNA in cloned cells belongs to an older individual,  the cloned individual’s life expectancy may be affected. Indeed, analysis of Dolly’s DNA revealed shorter...
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Introduction to Nuclear Reprogramming01:14

Introduction to Nuclear Reprogramming

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Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
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関連する実験動画

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クローン に 歩み を 教える

James E Crowe1

  • 1Departments of Pediatrics, Pathology, Microbiology, and Immunology and Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

Cell
|September 10, 2016
PubMed
まとめ

効果的なHIVワクチンを開発するには 抗体生成の課題を克服する必要があります HIVワクチンの戦略として 順次ブースティングの新型構造設計が期待されています

科学分野:

  • 免疫学
  • ウイルス学
  • ワクチン開発

背景:

  • 広範な中和抗体 (bNAbs) は,HIV感染の制御に不可欠です.
  • 自然なHIV感染は,通常,bNAbの発現のために,様々なウイルスの変異に長期にわたる曝露を必要とします.

研究 の 目的:

  • 強力なHIVを中和する抗体を誘発するための構造ベースの抗原設計を探求する.
  • HIVワクチンの戦略として,漸進的に成熟する抗原を配列的に増強するレジメントを調査する.

主な方法:

  • HIV抗原の構造ベースの計算設計
  • 連続抗原増強で動物モデルを免疫化する.
  • 中和の幅と効能を含む抗体反応の分析.

主要な成果:

  • 特定の抗体系を誘発する新しいHIV抗原を成功裏に設計した.
  • bNAbsに対する抗体開発を誘導することが示された.
  • 非順序的な治療法と比較して,様々なHIV株の強化された中和化を達成した.

結論:

  • 構造に基づく抗原設計は 効果的なHIVワクチン開発の 実行可能なアプローチです

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  • 最適化された抗原を配列的に増強する戦略は HIVワクチン開発の有望な道を示しています