IVI-Valencia, Institut Universitari IVI, Valencia, Spain.
Fertil Steril. 2012 Jan;97(1):74-8. doi: 10.1016/j.fertnstert.2011.10.006. Epub 2011 Oct 26.
To assess the presence of viral RNA or DNA sequences in spent culture media used after ovum pickup (OPU) or embryo culture and in liquid nitrogen (LN) used for oocyte or embryo vitrification in patients seropositive for human immunodeficiency virus (HIV), hepatitis C virus (HCV), and hepatitis B virus (HBV) undergoing IVF cycles.
Descriptive study.
Private university-affiliated IVF center.
PATIENT(S): Twenty-four women who underwent controlled ovarian stimulation for oocyte vitrification or IVF/ET. A total of 6, 11, and 6 patients were seropositive for HIV, HCV, and HBV, respectively, whereas 1 patient showed a coinfection with HCV and HBV. Seven patients presented positive blood viral load (HIV, n = 1; HBV, n = 1; HCV, n = 5). Sixty-three samples were analyzed: follicular fluid, n = 3; spent culture media, n = 33 (20 after OPU and 13 after embryo culture); and LN, n = 27 (14 and 10 after oocyte and embryo vitrification; and 3 LN storage tank samples).
INTERVENTION(S): Ovum pickup, oocyte and/or embryo culture, and/or vitrification by the Cryotop open device. Reverse transcription-polymerase chain reaction analysis was performed for viral screening.
MAIN OUTCOME MEASURE(S): Detection of viral sequences of HIV, HCV, and HVB.
RESULT(S): All the samples analyzed tested negative for the detection of viral RNA or DNA sequences.
CONCLUSION(S): We have not detected viral sequences after culture and vitrification of oocytes/embryos from HIV-, HBV-, and HCV-seropositive patients. These findings represent good evidence of the lack of risk of cross-contamination among seropositive patients, even using an open device for vitrification.
评估人类免疫缺陷病毒(HIV)、丙型肝炎病毒(HCV)和乙型肝炎病毒(HBV)血清阳性患者行体外受精(IVF)周期时,取卵(OPU)后或胚胎培养后废弃的培养液和用于卵母细胞或胚胎玻璃化冷冻的液氮(LN)中是否存在病毒 RNA 或 DNA 序列。
描述性研究。
私立大学附属 IVF 中心。
24 名接受卵母细胞玻璃化冷冻或 IVF/ET 的控制性卵巢刺激的女性。共有 6、11 和 6 名患者分别 HIV、HCV 和 HBV 血清阳性,1 名患者同时感染 HCV 和 HBV。7 名患者表现出阳性血病毒载量(HIV,n = 1;HBV,n = 1;HCV,n = 5)。分析了 63 个样本:卵泡液,n = 3;废弃的培养液,n = 33(20 个取自 OPU 后,13 个取自胚胎培养后);LN,n = 27(14 个和 10 个取自卵母细胞和胚胎玻璃化冷冻后;3 个 LN 储液罐样本)。
OPU、卵母细胞和/或胚胎培养以及 Cryotop 开放式设备进行的玻璃化。逆转录-聚合酶链反应分析用于病毒筛查。
检测 HIV、HCV 和 HBV 的病毒序列。
所有分析的样本均未检测到病毒 RNA 或 DNA 序列。
我们未在 HIV、HBV 和 HCV 血清阳性患者的卵母细胞/胚胎培养和玻璃化后检测到病毒序列。这些发现表明,即使使用开放式设备进行玻璃化,阳性血清患者之间也不存在交叉污染的风险。