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1.
Zhonghua Yu Fang Yi Xue Za Zhi ; 57(10): 1565-1570, 2023 Oct 06.
Article in Chinese | MEDLINE | ID: mdl-37859372

ABSTRACT

Objective: To explore the reentry rate of reactive blood donors in the bloodborne pathogen infection screening in Hangzhou City, and analyze the donation behavior of those who successfully returned. Methods: A retrospective analysis of the return data of blood donors with reactive bloodborne pathogen screening markers was conducted at Zhejiang Provincial Blood Center from June 2017 to May 2022. The reentry process for blood donors with reactive bloodborne pathogen screening markers in Hangzhou City is as follows: after the initial screening period of 6 months, donors can voluntarily apply for return to the blood center. Samples are collected and subjected to routine enzyme-linked immunosorbent assay (ELISA) screening for HBsAg, anti-HCV, HIV Ab/Ag, and anti-TP, as well as a single nucleic acid (HIV/HCV/HBV) test. For samples that show non-reactivity in both ELISA and nucleic acid tests, serum biomarker testing for the reasons of exclusion is performed using chemiluminescence immunoassay (CLIA), and those with non-reactivity are allowed to return. Results: A total of 4 583 reactive blood donors who met the criteria for re-entry applied for reentry, out of which 475 applications were received from donors in the Hangzhou area. Among these, 279 donors were successfully readmitted, resulting in a success rate of 58.74% (279/475). By the end of December 2021, out of the 174 donors who successfully returned, 114 donors chose to donate again. They collectively donated 39 530 ml of whole blood and 1 147.2 therapeutic doses of platelets. Among these, 21 donors once again showed reactivity for pathogen infection biomarkers, accounting for 18.42% (21/114). Conclusion: The reentry strategy has somewhat mitigated the attrition of blood donors. Nevertheless, there are instances where donors who were successfully readmitted show reactivity once more in the screening for pathogen infection biomarkers.


Subject(s)
HIV Infections , Nucleic Acids , Humans , Blood Donors , Blood-Borne Pathogens , Retrospective Studies , Mass Screening/methods , Biomarkers , Hepatitis B virus
2.
HLA ; 2018 May 22.
Article in English | MEDLINE | ID: mdl-29790279

ABSTRACT

HLA-A*02:625 differs from HLA-A*02:06:01:01 by a single nucleotide substitution at position 806 C>T.

3.
Int J Immunogenet ; 45(3): 143-145, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29676515

ABSTRACT

A novel allelic variant in HLA-B*40 lineage, HLA-B*40:298:02, has been identified in an individual of Han ethnicity afflicted with nasopharyngeal carcinoma in Hunan province, southern China. Following polymerase chain reaction-Sanger sequence-based typing (PCR-SBT), this new variant was further confirmed by two distinct strategies of cloning and sequencing. HLA-B*40:298:02 differs from HLA-B*40:298:01 by a single synonymous cytosine substitution at nucleotide position 26 (T→C) in exon 3, which corresponds to codon 99 of the mature HLA-B mRNA molecule. This new allele has an estimated frequency of 0.0002, in about 2,500 sequence-based typed subjects from the same population.


Subject(s)
Alleles , Genetic Variation , HLA-B Antigens/genetics , Amino Acid Sequence , Cloning, Molecular , Codon , Exons , HLA-B Antigens/chemistry , Humans , Male , Middle Aged , Sequence Analysis, DNA
4.
HLA ; 91(6): 543-544, 2018 06.
Article in English | MEDLINE | ID: mdl-29464869
5.
HLA ; 91(4): 302-303, 2018 04.
Article in English | MEDLINE | ID: mdl-29417749

ABSTRACT

HLA-B*40:333 differs from HLA-B*40:01:01 by a single nucleotide substitution at position 380 T>C.


Subject(s)
Alleles , HLA-B Antigens/genetics , Histocompatibility Testing/methods , Polymerase Chain Reaction/methods , Base Sequence , Exons/genetics , Genetic Loci , Humans , Sequence Alignment
6.
HLA ; 91(4): 303-305, 2018 04.
Article in English | MEDLINE | ID: mdl-29292580

ABSTRACT

HLA-B*40:338N differs from HLA-B*40:01:01 by a single nucleotide substitution at position 843C>A.


Subject(s)
Alleles , Asian People/genetics , HLA-B Antigens/genetics , Leukemia/genetics , Base Sequence , Exons/genetics , Humans , Sequence Alignment
7.
HLA ; 91(2): 136-137, 2018 02.
Article in English | MEDLINE | ID: mdl-29193787

ABSTRACT

HLA-B*27:04:06 differs from HLA-B*27:04:01 by a single-nucleotide substitution at position 396 C > A.


Subject(s)
Alleles , Asian People/genetics , Bone Marrow/metabolism , HLA-B Antigens/genetics , Tissue Donors , Base Sequence , Exons/genetics , Humans
8.
HLA ; 91(2): 142-143, 2018 02.
Article in English | MEDLINE | ID: mdl-29220119

ABSTRACT

HLA-DQB1*03:181 has one nucleotide change from HLA-DQB1*03:05:01 at position 470C>G.


Subject(s)
Alleles , Asian People/genetics , HLA-DQ beta-Chains/genetics , Leukemia/genetics , Base Sequence , Exons/genetics , Humans
9.
HLA ; 91(2): 133-134, 2018 02.
Article in English | MEDLINE | ID: mdl-29243881

ABSTRACT

HLA-B*13:98 differs from HLA-B*13:02:01 by a single nucleotide substitution at position 193 A>G.


Subject(s)
Alleles , Asian People/genetics , HLA-B Antigens/genetics , Base Sequence , Exons/genetics , Humans
10.
Int J Immunogenet ; 44(6): 356-358, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29086483

ABSTRACT

A novel HLA-B*39:01:01-related variant, HLA-B*39:130, has been identified in a normal individual of Han ethnicity in Hunan province, southern China. Following Sanger polymerase chain reaction-sequence-based typing (PCR-SBT), this new allele was further confirmed by cloning, phasing and sequencing. Aligned with HLA-B*39:01:01, HLA-B*39:130 has a nonsynonymous thymine substitution at nucleotide position 94 in exon 4, resulting in amino acid change from threonine to isoleucine at codon 214 (ACA→ATA) of the mature HLA-BmRNA molecule.


Subject(s)
Alleles , HLA-B Antigens/genetics , Adult , Base Sequence , Cloning, Molecular , Humans , Male
11.
HLA ; 90(2): 118-120, 2017 08.
Article in English | MEDLINE | ID: mdl-28371366

ABSTRACT

HLA-B*40:01:41 differs from HLA-B*40:01:01 by a single nucleotide substitution at position 195 G>A.


Subject(s)
Alleles , Genotyping Techniques , HLA-B40 Antigen/genetics , Polymerase Chain Reaction , Asian People , Blood Donors , Fetal Blood , Humans
12.
Int J Immunogenet ; 44(3): 145-147, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28371368

ABSTRACT

A new MICA allelic variant, MICA*007:07, was identified in an individual of Mongol ethnicity in the Inner Mongolia Autonomous Region, northern China. Following polymerase chain reaction-sequence-based typing (PCR-SBT), this new allele was further confirmed by cloning and sequencing. MICA*007:07 differs from MICA*007:01 by a synonymous mutation from G to A at the 2nd nucleotide position in exon 2. MICA*007:07 was linked to HLA-B*27:05.


Subject(s)
Base Sequence/genetics , HLA-B Antigens/genetics , Histocompatibility Antigens Class I/genetics , Cloning, Molecular , Exons , Female , HLA-B Antigens/immunology , Histocompatibility Antigens Class I/immunology , Humans , Linkage Disequilibrium
13.
HLA ; 90(2): 133-134, 2017 08.
Article in English | MEDLINE | ID: mdl-28393488

ABSTRACT

HLA-DRB1*15:127 has 1 nucleotide change from HLA-DRB1*15:01:01:01 at position 308 C>G.


Subject(s)
Alleles , Bone Marrow , Genotyping Techniques , HLA-DRB1 Chains/genetics , Polymerase Chain Reaction , Tissue Donors , China , Humans
14.
HLA ; 90(2): 115-116, 2017 08.
Article in English | MEDLINE | ID: mdl-28425190

ABSTRACT

HLA-B*27:147 differs from HLA-B*27:04:01 by a single nucleotide substitution at position 523 C>G.


Subject(s)
Alleles , Genotyping Techniques/methods , HLA-B27 Antigen/genetics , Polymerase Chain Reaction/methods , Humans
20.
Proc Nutr Soc ; 76(3): 283-294, 2017 08.
Article in English | MEDLINE | ID: mdl-27938425

ABSTRACT

For nutrition practitioners and researchers, assessing dietary intake of children and adults with a high level of accuracy continues to be a challenge. Developments in mobile technologies have created a role for images in the assessment of dietary intake. The objective of this review was to examine peer-reviewed published papers covering development, evaluation and/or validation of image-assisted or image-based dietary assessment methods from December 2013 to January 2016. Images taken with handheld devices or wearable cameras have been used to assist traditional dietary assessment methods for portion size estimations made by dietitians (image-assisted methods). Image-assisted approaches can supplement either dietary records or 24-h dietary recalls. In recent years, image-based approaches integrating application technology for mobile devices have been developed (image-based methods). Image-based approaches aim at capturing all eating occasions by images as the primary record of dietary intake, and therefore follow the methodology of food records. The present paper reviews several image-assisted and image-based methods, their benefits and challenges; followed by details on an image-based mobile food record. Mobile technology offers a wide range of feasible options for dietary assessment, which are easier to incorporate into daily routines. The presented studies illustrate that image-assisted methods can improve the accuracy of conventional dietary assessment methods by adding eating occasion detail via pictures captured by an individual (dynamic images). All of the studies reduced underreporting with the help of images compared with results with traditional assessment methods. Studies with larger sample sizes are needed to better delineate attributes with regards to age of user, degree of error and cost.


Subject(s)
Diet Records , Diet/adverse effects , Internet , Mobile Applications , Portion Size , Adult , Biomedical Research/methods , Biomedical Research/trends , Cell Phone , Child , Child Nutritional Physiological Phenomena , Computers, Handheld , Congresses as Topic , Dietetics/methods , Dietetics/trends , Humans , Nutrition Assessment , Nutritional Sciences/methods , Nutritional Sciences/trends , Photography/instrumentation , Photography/trends , Societies, Scientific , Video Recording/instrumentation , Video Recording/trends
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