1.Screening analysis of irregular antibodies from random donor population in Shaoguan area.
Jian-Ying ZHU ; Jiong-Cai LAN ; Hong-Qing LUO
Journal of Experimental Hematology 2007;15(3):630-631
The study was purposed to analyze the frequency and distribution of irregular antibodies in Shaoguan area. Screening 15 033 random donor antibodies in Shaoguan area by screening cells, polybrene and antiglobulin tests. The results indicated that the irregular antibodies were found in 42 samples. The frequency of irregular antibodies in female was higher than that in male (P < 0.001), and Rh blood group antibodies such as anti-D, anti-E, and anti-Ec C were common (47.6%). 2 samples of Le antibodies were failed to be found by polybrene test. 2 samples of irregular antibodies with titer 2 were undiscovered by screening test of 10 pooled samples. In conclusion, because of irregular antibodies resulting in hemolytic transfusion reaction, the investigation of frequency and distribution of irregular antibodies is very important for safe transfusion. Antibody screening must be done for female donors, and especially for massive plasma transfusion of patients with severe and dangerous illness and infants so as to ensure safety.
Adolescent
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Adult
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Blood Donors
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China
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Erythrocytes
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immunology
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Female
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Humans
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Isoantibodies
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blood
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Male
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Mass Screening
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Middle Aged
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Rh-Hr Blood-Group System
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blood
;
immunology
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Rho(D) Immune Globulin
2.Observation of antibody screen of patients with autoimmune hemolytic anemia.
Shao-Ming YANG ; Jiong-Cai LAN ; Li-Ya HU ; Hong-Qing LOU
Journal of Experimental Hematology 2004;12(6):849-851
To observe of alloantibodies of patients with autoimmune hemolytic anemia (AIHA), the alloantibodies masked by autoiantibody were detected by using chloroquine elution test, and the specificity of autoantibody was identified by ether elution test. The results showed that 19 cases out of 38 patients with AIHA were positive detected by indirect antiglobulin test and in 7 cases of them alloantibodies in sera cases were found (1 case of anti-D, 4 cases of anti-E and 2 cases of anti-CE), in 5 cases of them alloantibody were detected carried blood group specificity (3 cases of anti-E, anti-C and anti-c 1 case respectively). In conclusion, detections of alloantibodies by chloroquine elution test and ether elution test were very important for transfusion safety in therapy of patients with AIHA.
ABO Blood-Group System
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Adolescent
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Adult
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Anemia, Hemolytic, Autoimmune
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immunology
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Autoantibodies
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blood
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Blood Grouping and Crossmatching
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methods
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Erythrocytes
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immunology
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Female
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Humans
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Isoantibodies
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blood
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Male
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Middle Aged
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Rh-Hr Blood-Group System
3.Research of Typing for HLA-A, -B on Cord Blood Lymphocytes
Jiong-Cai LAN ; Qian SUN ; Qian CHEN ; Zhi-Mei ZHANG ; Qiong CAO ; Rong XIA ; Da-Lin WU ; Tao WU
Journal of Experimental Hematology 2001;9(3):251-255
Serological typing for HLA-A, -B has been used for a long time. Recently with the developing of molecular biology technologies, HLA-A, -B typing is now turning to genotyping methods. In our study, the capacity of PCR-SSP in solving problems in HLA-A, -B typing with serological methes was evaluated. With this aim the serological method was compared with PCR-SSP in 102 cord blood samples, and the results showed that 18.6% of 102 cord blood samples can't give a satisfactory detection, for 14 samples, give discrepant results with the 2 methods. It is mainly due to weak expression of HLA class I cord blood lymphocytes and the cross reaction of some antigens. About B 15 group, the further study was made, it was found that most of the B 15 splits is wrongly disassigned, especially among the B62-B75, B75/*1511(+)-B75/*1511(-), B46-*1511 antigens. It was concluded that DNA typing is more preferable than serological typing, about B 15 group, the subtyping or high resolution typing can be fulfilled at first in China.
4.Investigation of the characteristics of Rh blood group of Uygur nationality in Xinjiang.
Jiong-Cai LAN ; Hua-You ZHOU ; Xu-Hua BAI ; Xiao-Ping CHEN ; Yan-Zhao XING
Journal of Experimental Hematology 2007;15(4):885-887
The study was to investigate the characteristics of Rh blood group of Uygur nationality in Xinjiang. 1 230 blood samples of Uygur nationality were studied by Rh serological typing, modified antiglobulin test, chloroform/trichloroethylene absorption elution test, upstream, downstream and hybrid Rhesus boxes, 10 exons of D gene, RHD(psi) pseudogene. The results showed that the frequency of RHD negative was 5.8%, and no Del type was found. The further investigation of 72 samples of RhD (-) found that ccee (57.02%) and Ccee (29.08%) phenotype as well as RHD(-)/RHD(-) genotype (94.44%) and complete deletion type of D gene exon (91.12%) were all in high frequency, no RHD(psi) pseudugene was detected. In conclusion, the Rh blood group of Uygurs nationality in Xinjiang possesses both oriental and caucasian Rh characteristics, which enriches the diversity of blood types in chinesenation.
Asian Continental Ancestry Group
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genetics
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China
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ethnology
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Gene Deletion
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Humans
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Rh-Hr Blood-Group System
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genetics
5.Correlation of newborn hemolytic disease with ABO antibodies in sera of pregnant women.
Shao-Ming YANG ; Qiao-Ying WU ; Hong-Qing LUO ; Jiong-Cai LAN
Journal of Experimental Hematology 2005;13(5):875-877
To investigate the relations between morbidity of hemolytic diseases of newborn and ABO antibodies (HDN) in sera of Han and Yao nationality, pregnant women were examined before and after delivery. Antibodies screen, direct antiglobulin test, free antibodies and elution test were all performed. The results indicated that immunologic ABO antibodies of Han people were found in 673 cases out of 1,471 Han pregnant women, and was also found in 28 cases out of 65 Yao pregnant women, and there was no significant difference of incidences between Han and Yao nationality. 31 cases of HDN were found out of 288 newborn in Han and 3 cases of HDN were found out of 25 newborn in Yao, and there was no significant difference between Han and Yao nationalities. The characteristics of HDN in Han nationality were as same as in Yao nationality. In conclusion, the morbidity of HDN in Han and Yao nationalities of Shaoguan area did not showed essential difference, the immunologic ABO antibodies and its titration test, especially, elution test are important for prognosis of HDN.
ABO Blood-Group System
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immunology
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Adult
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Blood Group Incompatibility
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blood
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congenital
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China
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Erythroblastosis, Fetal
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blood
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pathology
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Female
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Humans
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Immunoglobulin G
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blood
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Infant, Newborn
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Male
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Pregnancy
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Prognosis
6.Study on blood ABO typing in patients with autoimmune hemolytic anemia.
Jian-Ying ZHU ; Jiong-Cai LAN ; Li-Ya HU ; Qing-Bao MENG ; Hong-Qing LUO
Journal of Experimental Hematology 2004;12(4):525-527
To explore effect of autoantibody on identification of ABO and RhD blood group, the blood samples of 38 patients with autoimmune hemolytic anemia (AIHA) were identified by routine typing and typing after chloroquine elution test as well as PCR. The results showed that out of 38 patients with AIHA, 11 cases (31.6%) of ABO blood group were difficulty typed, indirect antiglobulin test were positive, and contradiction between cells typing and sera typing were observed. 1 case of RhD(-) was mistyped as RhD(+) and anti-D was found in its serum. The blood group of these cases were typed correctly by chloroquine elution test. It is concluded that blood group identification of patients with AIHA can be interfered by autoantibody, and the correct typing for blood group of these patients may be determined by using combination of several methods to ensure safe transfusion.
ABO Blood-Group System
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genetics
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Adolescent
;
Adult
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Anemia, Hemolytic, Autoimmune
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blood
;
Blood Grouping and Crossmatching
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Female
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Genotype
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Humans
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Male
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Middle Aged
;
Rh-Hr Blood-Group System
7.ABO blood group typing for infants and its application for clinical transfusion.
Yin-Ze ZHANG ; Jiong-Cai LAN ; Wei LI ; Zhong LIU ; Rong XIA ; Hua-You ZHOU
Journal of Experimental Hematology 2003;11(3):301-304
To study the correct method for determining ABO blood types in infants and its influencing factors, blood types of 33 infants under 6 months old were determined by routine serological method, micro-column gel typing system and PCR-SSP genotyping method. Of the 33 cases with discrepant results of ABO blood type by different methods, the blood types of 32 cases were discrepant between red cell and serological typings in the routine serological method, and a false coincidence in 1 case was caused by bacterial infection resulting in B-like antigen. Correct blood typing was obtained in 27 cases with a correct rate of 84.4% (27/32) by using micro-column gel typing system. PCR-SSP method gave correct results in all of 33 cases. There was a significant difference between the results of micro-column gel typing system and PCR-SSP. It is concluded that to determine ABO blood type for infants < 6 months old, it is recommended to adopt micro-column gel typing system method, and what must be taken into account is the possible false coincidence caused by bacterial infection resulting in B-like antigen. In micro-column gel typing system, if the results of red cell and serological typing are identical, the principle is that blood transfusion must be performed with same ABO blood type between recipient and donor. If not, washed O red blood cells should be used for infants, and then change to transfusion with identical blood group according to PCR-SSP typing results.
ABO Blood-Group System
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genetics
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Blood Grouping and Crossmatching
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methods
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Blood Transfusion
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DNA
;
genetics
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Female
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Humans
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Infant
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Infant, Newborn
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Male
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Polymerase Chain Reaction
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methods
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Reproducibility of Results
8.Separation and cryopreservation of cord blood mononuclear cells.
Jiong-Cai LAN ; Zhong LIU ; Mao-Zhou GAN ; Qiang CHEN ; Yin-Zhe ZHANG ; Qing-Bao MENG
Journal of Experimental Hematology 2002;10(4):351-354
The influencing factors on cord blood storage after collection and mononuclear cell separation as well as cryopreservation were studied. The mononuclear cell are separated from blood after blood collection, then cryopreserved and washed after thawed. Results showed that the cord blood kept at 4 degrees C or room temperature less than 24 hours after blood collection, mononuclear cell separated by hydroxyethylstarch and 2 centrifugations, mononuclear cell cryopreserved with 50% DMSO and autoplasma from cord blood as protectives and washing the cells after thawing. In conclusion, the optimal project in this study can effectively preserve cord blood mononuclear cells.
Blood Preservation
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Cell Separation
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methods
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Cryopreservation
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Fetal Blood
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cytology
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Humans
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Leukocytes, Mononuclear
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physiology
9.Comparison of Rhesus boxes in Hans and Uighurs.
Jiong-cai LAN ; Hua-you ZHOU ; Xu-hua BAI ; Gui-zhi PANG ; Xiao-zhu WANG ; Ling-jun CAI ; Qiong CAO ; Yin-ze ZHANG ; Rong XIA ; Quan-ke YANG
Chinese Journal of Medical Genetics 2005;22(5):580-582
OBJECTIVETo study the difference and similarity between Hans and Uighurs in regard to Rhesus box and its significance.
METHODSThe sequence specific primers of upstream, downstream and hybrid Rhesus boxes were designed on the basis of RHD gene sequence. The upstream, downstream and hybrid Rhesus boxes were determined by polymerase chain reaction-sequence specific primer(PCP-SSP) and mismatched PCR.
RESULTSThe percentage of RHD-/RHD-, RHD+/RHD- and RHD+/RHD+ genotypes ascertained in the unrelated Hans with RhD(-) were 61.40%, 34.21% and 4.39% respectively, while those in the unrelated Chinese Uighurs with RhD(-) were 94.44%, 2.78% and 2.78% respectively. Furthermore, all 6 cases of some other minorities were RHD-/RHD- types. The percentage of RHD-/RHD- and RHD+/RHD- genotypes ascertained in the unrelated Chinese Uighurs were significantly higher than those in Chinese Hans (P < 0.01), whereas no statistically significant difference in the percentage of RHD+/RDH+ genotype between the two groups was observed (P > 0.05).
CONCLUSIONThe Rh blood group of Uighurs in Xingjiang possesses both Oriental and Caucasian characteristics, which embodies a special ethnical aspect of the Chinese nation and is in accord with the anthropologic research results.
China ; Genetics, Population ; Genotype ; Humans ; Polymerase Chain Reaction ; Rh-Hr Blood-Group System ; genetics
10.Comparison between genotyping and serological phenotyping in RhCE blood group.
Hua-you ZHOU ; Yin-ze ZHANG ; Qing-bao MENG ; Xu-hua BAI ; Cong-rong WANG ; Qiong CAO ; Jiong-cai LAN
Chinese Journal of Medical Genetics 2008;25(1):66-69
OBJECTIVETo genotype the RHCE gene of Hans, Xinjiang's Uigurs and Kazakstans in China, and to compare the results of RHCE genotyping with that of RhCc/Ee phenotyping.
METHODSRHCE genes of 98 Hans with RhD positive and 230 Hans, 72 Uigurs and 18 Kazakstans with RhD/RHD negative were genotyped with PCR-sequence specific primer (SSP) technique.
RESULTSThe results of RHE/RHe genotyping from samples with RhD positive and negative were in accord with that of phenotyping. It would result in 4.44% error using C-->G polymorphism at nt48 of RHCE gene to genotype RHCE, and 4.05% failure of detection using the 109 bp insertion to detectRHCE gene in Chinese Hans. The results of RHE/RHe genotyping in unrelated 72 Uigurs and 18 Kazakstans with RhD phenotype were consistent with that of phenotyping, and false positive and false negative were not found in genotyping in Uigurs and Kazakstans tested.
CONCLUSIONThe results of RHE/RHe and RHc genotyping were correct with PCR-SSP and accordant with that of phenotyping. Using the C48G polymorphism in exon 1 of RHCE to genotype RHC gene would result in false positive resulting from RHc mutation at this locus, and using the 109 bp insertion to genotype RHC gene would result in false negative because of the absence of the 109 bp. Therefore it is necessary to genotype RHC gene using more than two polymorphic loci.
Ethnic Groups ; genetics ; Genotype ; Humans ; Phenotype ; Polymorphism, Genetic ; Rh-Hr Blood-Group System ; blood ; genetics ; Serologic Tests ; methods