Basic investigation of the lectin method for separation and recovery of nucleated red blood cells in maternal blood, and a study into the frequency of nucleated red blood cells in fetomaternal disorders
ABSTRACT We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean aggluti...
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Published in | Congenital anomalies Vol. 45; no. 1; pp. 26 - 31 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Melbourne, Australia
Blackwell Science Pty
01.03.2005
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Subjects | |
Online Access | Get full text |
ISSN | 0914-3505 1741-4520 |
DOI | 10.1111/j.1741-4520.2005.00057.x |
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Abstract | ABSTRACT We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean agglutinin, 7 mL of maternal peripheral blood was collected from 20 subjects, and the relative fluorescence intensity was measured using flowcytometry; 50 mg/mL, used in previous studies, was the optimal concentration. The number of cells recovered at each step of the lectin method was also investigated by FACS using fluorescence‐labeled CD11a and CD33, and the results showed the usefulness of the method. Next, 7 mL of maternal peripheral blood was collected from 292 women with a normal single pregnancy (389 specimens), and NRBCs were separated and recovered using the lectin method. NRBCs slightly increased over the course of pregnancy (y = 4.29x + 5.03, r2 = 0.11). When blood was collected multiple times in the same subjects, NRBCs increased in 63 of 77 subjects (83.1%, percent change: 2.4 ± 19.0). No NRBCs were recovered in 17 subjects (4.7%). Regarding the relationship between fetomaternal disorders and the frequency of NRBCs, 89.4 ± 92.6 cells appeared per 10 mL of maternal blood in the normal group, but NRBCs increased in patients with 18 trisomy, placenta previa, pre‐eclampsia, intrauterine fetal death, and 21 trisomy. NRBC examination may play an assisting role not only in fetal diagnosis but also in fetomaternal diagnosis. |
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AbstractList | We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean agglutinin, 7 mL of maternal peripheral blood was collected from 20 subjects, and the relative fluorescence intensity was measured using flowcytometry; 50 mg/mL, used in previous studies, was the optimal concentration. The number of cells recovered at each step of the lectin method was also investigated by FACS using fluorescence-labeled CD11a and CD33, and the results showed the usefulness of the method. Next, 7 mL of maternal peripheral blood was collected from 292 women with a normal single pregnancy (389 specimens), and NRBCs were separated and recovered using the lectin method. NRBCs slightly increased over the course of pregnancy (y = 4.29x + 5.03, r2 = 0.11). When blood was collected multiple times in the same subjects, NRBCs increased in 63 of 77 subjects (83.1%, percent change: 2.4 +/- 19.0). No NRBCs were recovered in 17 subjects (4.7%). Regarding the relationship between fetomaternal disorders and the frequency of NRBCs, 89.4 +/- 92.6 cells appeared per 10 mL of maternal blood in the normal group, but NRBCs increased in patients with 18 trisomy, placenta previa, pre-eclampsia, intrauterine fetal death, and 21 trisomy. NRBC examination may play an assisting role not only in fetal diagnosis but also in fetomaternal diagnosis. ABSTRACT We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean agglutinin, 7 mL of maternal peripheral blood was collected from 20 subjects, and the relative fluorescence intensity was measured using flowcytometry; 50 mg/mL, used in previous studies, was the optimal concentration. The number of cells recovered at each step of the lectin method was also investigated by FACS using fluorescence‐labeled CD11a and CD33, and the results showed the usefulness of the method. Next, 7 mL of maternal peripheral blood was collected from 292 women with a normal single pregnancy (389 specimens), and NRBCs were separated and recovered using the lectin method. NRBCs slightly increased over the course of pregnancy (y = 4.29x + 5.03, r2 = 0.11). When blood was collected multiple times in the same subjects, NRBCs increased in 63 of 77 subjects (83.1%, percent change: 2.4 ± 19.0). No NRBCs were recovered in 17 subjects (4.7%). Regarding the relationship between fetomaternal disorders and the frequency of NRBCs, 89.4 ± 92.6 cells appeared per 10 mL of maternal blood in the normal group, but NRBCs increased in patients with 18 trisomy, placenta previa, pre‐eclampsia, intrauterine fetal death, and 21 trisomy. NRBC examination may play an assisting role not only in fetal diagnosis but also in fetomaternal diagnosis. ABSTRACT We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean agglutinin, 7 mL of maternal peripheral blood was collected from 20 subjects, and the relative fluorescence intensity was measured using flowcytometry; 50 mg/mL, used in previous studies, was the optimal concentration. The number of cells recovered at each step of the lectin method was also investigated by FACS using fluorescence‐labeled CD11a and CD33, and the results showed the usefulness of the method. Next, 7 mL of maternal peripheral blood was collected from 292 women with a normal single pregnancy (389 specimens), and NRBCs were separated and recovered using the lectin method. NRBCs slightly increased over the course of pregnancy ( y = 4.29x + 5.03, r 2 = 0.11). When blood was collected multiple times in the same subjects, NRBCs increased in 63 of 77 subjects (83.1%, percent change: 2.4 ± 19.0). No NRBCs were recovered in 17 subjects (4.7%). Regarding the relationship between fetomaternal disorders and the frequency of NRBCs, 89.4 ± 92.6 cells appeared per 10 mL of maternal blood in the normal group, but NRBCs increased in patients with 18 trisomy, placenta previa, pre‐eclampsia, intrauterine fetal death, and 21 trisomy. NRBC examination may play an assisting role not only in fetal diagnosis but also in fetomaternal diagnosis. We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean agglutinin, 7 mL of maternal peripheral blood was collected from 20 subjects, and the relative fluorescence intensity was measured using flowcytometry; 50 mg/mL, used in previous studies, was the optimal concentration. The number of cells recovered at each step of the lectin method was also investigated by FACS using fluorescence-labeled CD11a and CD33, and the results showed the usefulness of the method. Next, 7 mL of maternal peripheral blood was collected from 292 women with a normal single pregnancy (389 specimens), and NRBCs were separated and recovered using the lectin method. NRBCs slightly increased over the course of pregnancy (y = 4.29x + 5.03, r2 = 0.11). When blood was collected multiple times in the same subjects, NRBCs increased in 63 of 77 subjects (83.1%, percent change: 2.4 +/- 19.0). No NRBCs were recovered in 17 subjects (4.7%). Regarding the relationship between fetomaternal disorders and the frequency of NRBCs, 89.4 +/- 92.6 cells appeared per 10 mL of maternal blood in the normal group, but NRBCs increased in patients with 18 trisomy, placenta previa, pre-eclampsia, intrauterine fetal death, and 21 trisomy. NRBC examination may play an assisting role not only in fetal diagnosis but also in fetomaternal diagnosis.We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we verified the lectin method and investigated the appearance of NRBCs during pregnancy. For the concentration of lectin soy bean agglutinin, 7 mL of maternal peripheral blood was collected from 20 subjects, and the relative fluorescence intensity was measured using flowcytometry; 50 mg/mL, used in previous studies, was the optimal concentration. The number of cells recovered at each step of the lectin method was also investigated by FACS using fluorescence-labeled CD11a and CD33, and the results showed the usefulness of the method. Next, 7 mL of maternal peripheral blood was collected from 292 women with a normal single pregnancy (389 specimens), and NRBCs were separated and recovered using the lectin method. NRBCs slightly increased over the course of pregnancy (y = 4.29x + 5.03, r2 = 0.11). When blood was collected multiple times in the same subjects, NRBCs increased in 63 of 77 subjects (83.1%, percent change: 2.4 +/- 19.0). No NRBCs were recovered in 17 subjects (4.7%). Regarding the relationship between fetomaternal disorders and the frequency of NRBCs, 89.4 +/- 92.6 cells appeared per 10 mL of maternal blood in the normal group, but NRBCs increased in patients with 18 trisomy, placenta previa, pre-eclampsia, intrauterine fetal death, and 21 trisomy. NRBC examination may play an assisting role not only in fetal diagnosis but also in fetomaternal diagnosis. |
Author | Ikeya, Miki Shinya, Masaru Kitagawa, Michihiro |
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References | Simchen MJ, Barkai G, Lusky A, Guetta E (2001) Fetal hemoglobin-expressing nucleated red blood cell frequencies in pregnancies with intrauterine growth restriction. Prenat Diagn 21: 31-35. Goodfellow CF, Taylor PV (1982) Extraction and identification of trophoblast cells in peripheral blood during pregnancy. Br J Obstet Gynaecol 89: 65-68. Wada S, Kitagawa M (2004) A method of separation and concentration of fetal nucleated red blood cells in maternal blood and its application to fetal diagnosis. Congenit Anom (Kyoto) 6: 125-130. Bianchi DW, Stewart JE, Garber MF, Lucotte G, Flint AF (1991) Possible effect of gestational age on the detection of fetal nucleated erythrocytes in maternal blood. Prenat Diagn 11: 523-528. Kuo PL (1998) Frequencies of fetal nucleated red blood cells in maternal blood during different stages of gestation. Fetal Diagn Ther 13: 375-379. Wachi T, Kitagawa M (2004) Studies on preliminary concentration method for recovery of fetal nucleated red blood cells in maternal blood. Congenit Anom Kyoto 44: 142-146. Lotan R, Siegelman HW, Lis H, Sharon N (1974) Subunit structure of soybean agglutinin. J Biol Chem 294: 1219-1224. Pearson HA (1967) Life-span of the fetal red blood cell. J Pediatr 70: 166-171. Shulman LP, Phillip OP, Tolley E, Sammons D, Wachtel SS (1998) Frequency of nucleated red blood cells in maternal blood during the different gestational ages. Hum Genet 103: 723-726. Gänshirt-Ahlert D, Burschkyk M, Garritsen HSP et al. (1992) Magnetic cell sorting and transferring receptor as potential means of prenatal diagnosis from maternal blood. Am J Obstet Gynecol 166: 1350-1355. Zou L, Ye X, Zhu J (2000) Isolation of fetal nucleated red blood cells from maternal blood. J Tongji Med Univ 20: 169-171. Rodriguez de Alba M, Palomino P, Gonzalez-Gonzalez C et al. (2001) Prenatal diagnosis on fetal cells from maternal blood: Practical comparative evaluation of the first and second trimesters. Prenat Diagn 21: 165-170. Hamada H, Arinami T, Kubo T, Hamaguchi H, Iwasaki H (1993) Fetal nucleated cells in maternal peripheral blood: Frequency and relationship to gestational age. Hum Genet 91: 427-432. Takabayashi H, Kuwabara S, Ukita T, Ikawa K, Yamafuji K, Igarashi T (1995) Development of non-invasive fetal DNA diagnosis from maternal blood. Prenat Diagn 15: 74-77. Miltenyi S, Müller W, Weichel W, Radbruch A (1990) High gradient magnetic cell separation with MACS. Cytometry 11: 231-238. Douglas GW, Thomas L, Carr M, Cullen NM, Morris R (1959) Trophoblast in the circulating blood during pregnancy. Am J Obstet Gynecol 78: 960-969. Al-Mulfi R, Hambley H, Albaiges G, Lees C, Nicolaides KH (2000) Increased fetal erythroblasts in women who subsequently develop pre-eclampsia. Hum Reprod 15: 1624-1628. Hromadnikova I, Sedlackova L, Mrstinova M et al. (2000) Levels of peripheral circulating nucleated erythrocytes in pregnant women for noninvasive prenatal diagnosis. Ceska Gynekol 65: 33-37. O'Reilly RJ, Collins NH, Kernan N et al. (1985) Transplantation of marrow-depleted T cells by soybean lectin agglutination and E-rosette depletion: Major histocompatibility complex-related graft resistance in leukemic transplant recipients. Transplant Proc 17: 455-459. Jansen M, Korver-Hkkennes K, Leenen DV et al. (2001) Significantly higher number of fetal cells in the maternal circulation of women with pre-eclampsia. Prenat Diagn 21: 1022-1026. Bianchi DW (1997) Prenatal diagnosis by the isolation of fetal cells in the maternal circulation. Progresos En Obsterica y Ginecologia 40: 16-23. Kitagawa M, Sugiura K, Omi H et al. (2002) New technique using galactose-specific lectin for isolation of fetal cells from maternal blood. Prenat Diagn 22: 17-21. Iverson GM, Bianchi DW, Cann HM, Herzenberg L (1981) Detection and isolation of fetal cells from maternal blood using the fluorescence activated cell sorter (FACS). Prenat Diagn 1: 61-73. Prieto B, Candenas M, Venta R, Ladenson JH, Alvarez FV (2002) Isolation of fetal nucleated red cells from maternal blood in normal and aneuploid pregnancies. Clin Chem Lab Med 40: 667-672. Schroder J, Chapelle AD (1972) Fetal lymphocytes in the maternal blood. Blood 39: 153-161. 1982; 89 2004; 44 1985; 17 1967; 70 1997; 40 1990; 11 2000; 15 1981; 1 1995; 15 1991; 11 1992; 166 2002; 40 2000; 65 2002; 22 2000; 20 2004; 6 1993; 91 1998; 103 1972; 39 1959; 78 1974; 294 2001; 21 1998; 13 Schroder J (e_1_2_6_20_1) 1972; 39 e_1_2_6_10_1 Hromadnikova I (e_1_2_6_9_1) 2000; 65 Bianchi DW (e_1_2_6_3_1) 1997; 40 e_1_2_6_19_1 O'Reilly RJ (e_1_2_6_16_1) 1985; 17 e_1_2_6_13_1 e_1_2_6_11_1 e_1_2_6_12_1 e_1_2_6_17_1 e_1_2_6_18_1 e_1_2_6_15_1 e_1_2_6_21_1 e_1_2_6_8_1 Wada S (e_1_2_6_25_1) 2004; 6 e_1_2_6_5_1 e_1_2_6_4_1 e_1_2_6_7_1 e_1_2_6_6_1 e_1_2_6_24_1 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_22_1 Lotan R (e_1_2_6_14_1) 1974; 294 e_1_2_6_26_1 |
References_xml | – reference: Gänshirt-Ahlert D, Burschkyk M, Garritsen HSP et al. (1992) Magnetic cell sorting and transferring receptor as potential means of prenatal diagnosis from maternal blood. Am J Obstet Gynecol 166: 1350-1355. – reference: O'Reilly RJ, Collins NH, Kernan N et al. (1985) Transplantation of marrow-depleted T cells by soybean lectin agglutination and E-rosette depletion: Major histocompatibility complex-related graft resistance in leukemic transplant recipients. Transplant Proc 17: 455-459. – reference: Shulman LP, Phillip OP, Tolley E, Sammons D, Wachtel SS (1998) Frequency of nucleated red blood cells in maternal blood during the different gestational ages. Hum Genet 103: 723-726. – reference: Kuo PL (1998) Frequencies of fetal nucleated red blood cells in maternal blood during different stages of gestation. Fetal Diagn Ther 13: 375-379. – reference: Schroder J, Chapelle AD (1972) Fetal lymphocytes in the maternal blood. Blood 39: 153-161. – reference: Takabayashi H, Kuwabara S, Ukita T, Ikawa K, Yamafuji K, Igarashi T (1995) Development of non-invasive fetal DNA diagnosis from maternal blood. Prenat Diagn 15: 74-77. – reference: Lotan R, Siegelman HW, Lis H, Sharon N (1974) Subunit structure of soybean agglutinin. J Biol Chem 294: 1219-1224. – reference: Wachi T, Kitagawa M (2004) Studies on preliminary concentration method for recovery of fetal nucleated red blood cells in maternal blood. Congenit Anom Kyoto 44: 142-146. – reference: Pearson HA (1967) Life-span of the fetal red blood cell. J Pediatr 70: 166-171. – reference: Al-Mulfi R, Hambley H, Albaiges G, Lees C, Nicolaides KH (2000) Increased fetal erythroblasts in women who subsequently develop pre-eclampsia. Hum Reprod 15: 1624-1628. – reference: Hamada H, Arinami T, Kubo T, Hamaguchi H, Iwasaki H (1993) Fetal nucleated cells in maternal peripheral blood: Frequency and relationship to gestational age. Hum Genet 91: 427-432. – reference: Iverson GM, Bianchi DW, Cann HM, Herzenberg L (1981) Detection and isolation of fetal cells from maternal blood using the fluorescence activated cell sorter (FACS). Prenat Diagn 1: 61-73. – reference: Zou L, Ye X, Zhu J (2000) Isolation of fetal nucleated red blood cells from maternal blood. J Tongji Med Univ 20: 169-171. – reference: Wada S, Kitagawa M (2004) A method of separation and concentration of fetal nucleated red blood cells in maternal blood and its application to fetal diagnosis. Congenit Anom (Kyoto) 6: 125-130. – reference: Miltenyi S, Müller W, Weichel W, Radbruch A (1990) High gradient magnetic cell separation with MACS. Cytometry 11: 231-238. – reference: Simchen MJ, Barkai G, Lusky A, Guetta E (2001) Fetal hemoglobin-expressing nucleated red blood cell frequencies in pregnancies with intrauterine growth restriction. Prenat Diagn 21: 31-35. – reference: Bianchi DW, Stewart JE, Garber MF, Lucotte G, Flint AF (1991) Possible effect of gestational age on the detection of fetal nucleated erythrocytes in maternal blood. Prenat Diagn 11: 523-528. – reference: Jansen M, Korver-Hkkennes K, Leenen DV et al. (2001) Significantly higher number of fetal cells in the maternal circulation of women with pre-eclampsia. Prenat Diagn 21: 1022-1026. – reference: Douglas GW, Thomas L, Carr M, Cullen NM, Morris R (1959) Trophoblast in the circulating blood during pregnancy. Am J Obstet Gynecol 78: 960-969. – reference: Bianchi DW (1997) Prenatal diagnosis by the isolation of fetal cells in the maternal circulation. Progresos En Obsterica y Ginecologia 40: 16-23. – reference: Rodriguez de Alba M, Palomino P, Gonzalez-Gonzalez C et al. (2001) Prenatal diagnosis on fetal cells from maternal blood: Practical comparative evaluation of the first and second trimesters. 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Snippet | ABSTRACT We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present... ABSTRACT We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present... We previously reported the separation and recovery of nucleated red blood cells (NRBCs) in maternal blood using the lectin method. In the present study, we... |
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SubjectTerms | Cell Nucleus - pathology Cell Separation - methods Erythrocyte Count Erythrocytes - pathology FACS Female Fetal Blood - cytology Flow Cytometry - methods Fluorescein-5-isothiocyanate Gestational Age Humans lectin method Lectins Maternal-Fetal Exchange NRBC Plant Lectins Pregnancy Pregnancy Complications - blood Pregnancy Complications - diagnosis SBA Soybean Proteins |
Title | Basic investigation of the lectin method for separation and recovery of nucleated red blood cells in maternal blood, and a study into the frequency of nucleated red blood cells in fetomaternal disorders |
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