MATERNAL TRANSMISSION OF HTLV-1 OTHER THAN THROUGH BREAST-MILK - DISCREPANCY BETWEEN THE POLYMERASE CHAIN-REACTION POSITIVITY OF CORD BLOOD-SAMPLES FOR HTLV-1 AND THE SUBSEQUENT SEROPOSITIVITY OF INDIVIDUALS

被引:40
作者
KAWASE, K
KATAMINE, S
MORIUCHI, R
MIYAMOTO, T
KUBOTA, K
IGARASHI, H
DOI, H
TSUJI, Y
YAMABE, T
HINO, S
机构
[1] TOTTORI UNIV,FAC MED,DEPT VIROL,86 NISHI MACHI,YONAGO,TOTTORI 683,JAPAN
[2] NAGASAKI UNIV,SCH MED,DEPT BACTERIOL,NAGASAKI 852,JAPAN
[3] NAGASAKI UNIV,SCH MED,DEPT PEDIAT,NAGASAKI 852,JAPAN
[4] NAGASAKI UNIV,SCH MED,DEPT GYNECOL & OBSTET,NAGASAKI 852,JAPAN
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1992年 / 83卷 / 09期
关键词
CORD BLOOD; HTLV-1; MATERNAL TRANSMISSION; MILK-BORNE INFECTION; PCR;
D O I
10.1111/j.1349-7006.1992.tb02009.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We used a nested polymerase chain reaction (PCR) to diagnose HTLV-1 carriers. The DNA isolated from the nuclear extract obtained from frozen whole blood was found appropriate for PCR study both qualitatively and quantitatively. The use of freshly frozen whole blood made the field work much easier, and the use of a nuclear extraction procedure allowed DNA isolation in just 4 microcentrifuge tubes. We could not attain sufficient sensitivity to detect a single molecule with single-step PCR, but nested PCR was confirmed to detect a single molecule/reaction. All samples of the seropositive group including 94 blood donors, 66 mothers, and 13 children were positive in the nested PCR, while none of the seronegative group, including 198 blood donors and 285 children, was positive. Although 18/717 (2.5%) cord blood samples obtained from babies born to carrier mothers were PCR-positive, none of 5 formula-fed children tested who had been PCR-positive in the cord blood gave evidence of infection later on. Furthermore, all of 4 seropositive infected children who were formula-fed had been PCR-negative in their cord blood. The results are not consistent with intrauterine infection, but suggest the presence of a perinatal or postnatal infection route other than through breast milk.
引用
收藏
页码:968 / 977
页数:10
相关论文
共 48 条
[1]   ENZYMATIC GENE AMPLIFICATION - QUALITATIVE AND QUANTITATIVE METHODS FOR DETECTING PROVIRAL DNA AMPLIFIED INVITRO [J].
ABBOTT, MA ;
POIESZ, BJ ;
BYRNE, BC ;
KWOK, S ;
SNINSKY, JJ ;
EHRLICH, GD .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (06) :1158-1169
[2]  
ANDO Y, 1987, JPN J CANCER RES, V78, P322
[3]  
BEUTLER E, 1990, BIOTECHNIQUES, V9, P166
[4]   THE HUMAN TYPE-C RETROVIRUS, HTLV, IN BLACKS FROM THE CARIBBEAN REGION, AND RELATIONSHIP TO ADULT T-CELL LEUKEMIA LYMPHOMA [J].
BLATTNER, WA ;
KALYANARAMAN, VS ;
ROBERTGUROFF, M ;
LISTER, TA ;
GALTON, DAG ;
SARIN, PS ;
CRAWFORD, MH ;
CATOVSKY, D ;
GREAVES, M ;
GALLO, RC .
INTERNATIONAL JOURNAL OF CANCER, 1982, 30 (03) :257-264
[5]   PLATELET-DERIVED GROWTH FACTOR-A CHAIN - GENE STRUCTURE, CHROMOSOMAL LOCATION, AND BASIS FOR ALTERNATIVE MESSENGER-RNA SPLICING [J].
BONTHRON, DT ;
MORTON, CC ;
ORKIN, SH ;
COLLINS, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1492-1496
[6]   HOMOLOGY OF HUMAN T-CELL LEUKEMIA-VIRUS ENVELOPE GENE WITH CLASS-I HLA-GENE [J].
CLARKE, MF ;
GELMANN, EP ;
REITZ, MS .
NATURE, 1983, 305 (5929) :60-62
[7]  
FLEMING AF, 1983, LANCET, V2, P334
[8]  
FOLEY GE, 1965, CANCER, V18, P522, DOI 10.1002/1097-0142(196504)18:4<522::AID-CNCR2820180418>3.0.CO
[9]  
2-J
[10]   IMPROVEMENT OF GELATIN PARTICLE AGGLUTINATION-TEST FOR DETECTION OF ANTI-HTLV-I ANTIBODY [J].
FUJINO, R ;
KAWATO, K ;
IKEDA, M ;
MIYAKOSHI, H ;
MIZUKOSHI, M ;
IMAI, J .
JAPANESE JOURNAL OF CANCER RESEARCH, 1991, 82 (04) :367-370