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Screening for Antibodies to Human T-Cell Leukemia Virus Type I in Japanese Breast Milk

机译:日本母乳中人T细胞白血病病毒I型抗体的筛选

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Japanese breast milk samples were tested for antibodies to human T-cell leukemia virus type I (HTLV-1) by particle agglutination (PA) and a line immunoassay (LIA). In the PA method, the agglutination reaction between the HTLV-1 antibody and sensitized particles occurred at a 1:128 dilution of some breast milk sam-ples. The average antibody titer was one order of magnitude lower than that in the serum positive control. A total of 243 human breast milk specimens were assayed by PA, of which 21 samples from Okinawa, Hyogo, Miyagi and Hokkaido were positive or deferred. The results of the 21 positive samples were subsequently assayed by LIA (INNO-LIA~(TM) HTLV I/II) for confirmation; and one sample was positive, and two were indeterminate. We attempted to use polymerase chain reaction (PCR) to detect IITLV-I provirus DNA, but we did not detect PCR products for the pX1 region of the HTLV-1 genome in the LIA-positive samples. These negative PCR results are most likely due to the lower sensitivity of the PCR for amplification from milk than from HTLV-1-positive monocytes. In conclusion, the PA method to breast milk samples appears to be a suitable tool to screen for antibodies to HTLV-1 in the breast milk of carrier mothers in cases in which it would be difficult to use serum for the test. Although LIA may be able to confirm HTLV-1 infection, the presence of HTLV-1 provirus should be confirmed in the breast milk.
机译:通过颗粒凝集(PA)和线免疫分析(LIA)测试了日本母乳样品中的I型人T细胞白血病病毒(HTLV-1)抗体。在PA方法中,HTLV-1抗体与致敏颗粒之间的凝集反应发生在某些母乳样品的1:128稀释度下。平均抗体滴度比血清阳性对照低一个数量级。用PA分析了总共243个人类母乳样品,其中冲绳,兵库,宫城和北海道的21个样品为阳性或递延样品。随后通过LIA(INNO-LIA〜(TM)HTLV I / II)分析21个阳性样品的结果,以进行确认;一个样品为阳性,两个样品为不确定。我们试图使用聚合酶链反应(PCR)检测IITLV-1前病毒DNA,但未在LIA阳性样品中检测HTLV-1基因组pX1区的PCR产物。这些阴性PCR结果很可能是由于PCR对牛奶中扩增的敏感性低于HTLV-1阳性单核细胞。总之,在难以使用血清进行测试的情况下,对母乳样品进行PA方法似乎是一种合适的工具,可用于筛选母体母乳中HTLV-1的抗体。尽管LIA可能能够确认HTLV-1感染,但应在母乳中确认HTLV-1前病毒的存在。

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