1.Genotyping of 50 RhD variant samples: implication for transfusion ad pregnancy management
Ke WANG ; Xiaojie MA ; Hailin LI ; Jizhi WEN
Chinese Journal of Blood Transfusion 2025;38(12):1707-1712
Objective: To genotype 50 RhD variant samples from Guangzhou, China, using our previously established genotyping strategy, thereby providing guidance for transfusion management and antenatal monitoring in RhD-variant individuals. Methods: Between June and August 2024, fifty samples identified as RhD variants during RhD-negative confirmation testing at Guangzhou Blood Center were collected. Serological testing for the D antigen was performed with two different anti-D reagents, and the epitope profiles of the D antigen were determined using a commercial panel of monoclonal anti-D reagents containing nine kinds of monoclonal anti-D. Genomic DNA was extracted, and high-resolution melting (HRM) analysis was applied to detect the Asian-type DEL (RHD
1227A). Subsequently, RHD genotyping was carried out using Multiplex Ligation-dependent Probe Amplification (MLPA) and Sanger sequencing. Results: Among the 50 D variant samples, 17 (34.0%) Asian type DEL samples were detected by HRM, including 13 cases with RHD
DEL1/01N.01 genotype and 4 cases with RHD
DEL1/DEL1 genotype. Eleven (11/50, 22.0%) samples were typed as DVI by the epitope profiles of D antigen. The epitope profiles of D antigen combined with Sanger sequencing of exon 6 identified 5 (5/50, 10.0%) cases of RHD
weak partial 15/01N.01. MLPA combined with Sanger sequencing identified two cases of RHD
DVI.3/DEL1, representing 4.0% (2/50) of the samples. Additionally, the following RHD genotypes were each detected in one case: RHD
weak D type 18/01N.04, RHD
weak D type 72/01N.01, RHD
weak D type 95/DEL1, RHD
weak D type 114/DEL1, RHD
weak D type 136/DEL1, RHD
weak D type 147/01N.01, RHD
496G/496G, RHD
536C/01N.01, RHD
689A/689A, RHD
689A/DEL1, RHD
DEL32/DEL1, RHD
DV.1/01N.01, RHD
DV.5/01N.01, RHD
01.01/01N.01, and RHD
01/01N.01. Conclusion: Fifty D variant individuals were typed using our previously established serological and molecular approach. These findings provide guidance for precision transfusion therapy in RhD variant patients and inform evidence-based decisions regarding anti-D immunoglobulin prophylaxis for RhD variant pregnant women.
2.Shanghai community-based practice of early lung cancer screening with low-dose spiral computed tomography
Xiaoyang LUO ; Quan LIU ; Shengping WANG ; Yuan LI ; Lei SHEN ; Guodong LI ; Wentao LI ; Yanping ZHAO ; Huilin XU ; Hong FANG ; Guiqiang SHAO ; Jizhi CHU ; Junlei SUN ; Hongqi ZHU ; Zhiyong LI ; Lianghua JIANG ; Jianliang LING ; Weizhong ZHAO ; Jing WANG ; Xiaohua LIU ; Bin LI ; Yiliang ZHANG ; Ting YE ; Yunjian PAN ; Hong HU ; Rui WANG ; Yihua SUN ; Haiyan YANG ; Su XU ; Haiquan CHEN
China Oncology 2016;26(12):996-1003
Background and purpose:As one of the most fatal malignant tumors in China, the morbidity and mortality of lung cancer remain high. Early diagnosis and normative treatment is the key to improve the prognosis of lung cancer. The aim of this study was to explore the practice of early lung cancer screening with low-dose spiral computed tomography (CT) based on the current situation in community health service, with integration of superior resources of med-ical institutions at all levels in Shanghai.Methods:From Aug. 2013 to Aug. 2014, we screened high-risk population in selected communities of Minhang District, Shanghai, for early diagnosis of lung cancer with low-dose spiral CT combined with multidisciplinary comprehensive treatment models including minimally invasive surgery, exploring the medical service network covering prevention, diagnosis, treatment, rehabilitation and follow-up.Results:Screening population is 11 332 (male 7 144, female 4 188); Twenty-nine cases with pathological diagnosis of malignant tumor, including 27 cases of pri-mary lung cancer, 1 case of lung metastasis, 1 case of breast cancer. The morbidity of primary lung cancer is 238.26×10-5. There were 22 cases of Stage 0-Ⅰ lung cancer accounting for 81.48% of all diagnosed primary lung cancer.Conclusion:Based on community health service, screening with low-dose spiral CT could improve the early diagnosis rate of lung can-cer with feasibility and validity, which could be applicable in qualified eligible medical center and community in China.
3.INHIBITION OF FUNGAL FERMENTED FILTRATES ON PHYTOPHTHORA INFESTANS
Jizhi JIANG ; Likun ZHAO ; Juan SHI ; Jingao DONG
Microbiology 2001;28(2):55-59
Effect of 8 fungal fermented filtrates on mycelial growth, encystment and germination of zoospores, appressorium formation, and penetration hyphae formation of Phytophthora infestans was investigated. Of which, the fermented filtrates from Rhizoctonia solani and Colletotrichum gloeosporioides showed the strongest inhibition against P. infestans. The results indicated that they are potential for controlling the diseases caused by P. infestans.
4.Clinical application of Lappaconitine hydrobromide
Jizhi YU ; Baijing ZHANG ; Xuetao JIANG
Academic Journal of Second Military Medical University 2000;0(07):-
Lappaconitine hydrobromide can remove inflammation and swelling, lower temperature and relieve heat. It also can be used for local anesthesia. Clinically lappaconitine hydrobromide can be applied via i.v., i.m. or p.o. for analgesic treatment. Lappaconitine has better effect for moderate pain than for severe pain, which may be associated with the low dose. Future efforts should be made in increasing dosage, combining lappaconitine hydrobromide with other drugs and improving drug delivery technique.
5.Establishment of HEK293 cell line expressing sense and antisense Alu-Sx stably and efficiently
Liang PENG ; Gang WU ; Jizhi JIANG ; Fengshuo JIN ; Rui DING
Journal of Third Military Medical University 1988;0(06):-
Objective To establish a HEK293 cell line stably and highly expressing sense and antisense Alu-Sx.Methods According to Alu subfamily Sx sequence,a pair of primers containing the sites for given restrictive endonuclease at both ends were designed and synthesized.PCR of the total DNA extracted from HEK293 cell line was performed,the products of which were cloned into a highly efficient eukaryotic expression vector pcDNA3.1/myc-His A.The recombinants were sequenced and identified by restrictive endonuclease digestion and then transfected into the HEK293 cell line by lipofectamine2000.The stable transfectants were screened by G418.Cell subclones were isolated by gradient dilution.The highly expressing clones were identified by Northern blotting.Results Eukaryotic expressing vectors stably and efficiently expressing sense and antisense Alu-Sx were constructed and cell subclones stably and efficiently expressing sense and antisense Alu-Sx were established.Conclusion Cell subclones stably and efficiently expressing sense and antisense Alu-Sx can used for our further study.

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