RETRACTED: Patient-specific embryonic stem cells derived from human SCNT blastocysts (Retracted Article. See vol 311, pg 335, 2006)

被引:284
|
作者
Hwang, WS [1 ]
Roh, SI
Lee, BC
Kang, SK
Kwon, DK
Kim, S
Kim, SJ
Park, SW
Kwon, HS
Lee, CK
Lee, JB
Kim, JM
Ahn, C
Paek, SH
Chang, SS
Koo, JJ
Yoon, HS
Hwang, JH
Hwang, YY
Park, YS
Oh, SK
Kim, HS
Park, JH
Moon, SY
Schatten, G
机构
[1] Seoul Natl Univ, Coll Vet Med, Seoul 151742, South Korea
[2] Seoul Natl Univ, Sch Agr Biotechnol, Seoul 151742, South Korea
[3] MizMed Hosp, Med Res Ctr, Seoul 135280, South Korea
[4] Seoul Natl Univ, Coll Med, Seoul 110744, South Korea
[5] Hanna Womens Clin, Seoul 137872, South Korea
[6] Hanyang Univ, Sch Med, Seoul 471701, South Korea
[7] Univ Pittsburgh, Sch Med, Pittsburgh Dev Ctr, Magee Womens Res Inst,Dept Obstet Gynecol & Repro, Pittsburgh, PA 15213 USA
[8] Univ Pittsburgh, Sch Med, Dept Cell Biol & Physiol, Pittsburgh, PA 15213 USA
关键词
D O I
10.1126/science.1112286
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Patient-specific, immune-matched human embryonic stem cells (hESCs) are anticipated to be of great biomedical importance for studies of disease and development and to advance clinical deliberations regarding stem cell transplantation. Eleven hESC lines were established by somatic cell nuclear transfer (SCNT) of skin cells from patients with disease or injury into donated oocytes. These lines, nuclear transfer (NT)-hESCs, grown on human feeders from the same NT donor or from genetically unrelated individuals, were established at high rates, regardless of NT donor sex or age. NT-hESCs were pluripotent, chromosomally normal, and matched the NT patient's DNA. The major histocompatibility complex identity of each NT-hESC when compared to the patient's own showed immunological compatibility, which is important for eventual transplantation. With the generation of these NT-hESCs, evaluations of genetic and epigenetic stability can be made. Additional work remains to be done regarding the development of reliable directed differentiation and the elimination of remaining animal components. Before clinical use of these cells can occur, preclinical evidence is required to prove that transplantation of differentiated NT-hESCs can be safe, effective, and tolerated.
引用
收藏
页码:1777 / 1783
页数:7
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