journal
https://read.qxmd.com/read/26467895/determination-of-unacceptable-hla-antigen-mismatches-in-kidney-transplant-recipients-recommendations-of-the-german-society-for-immunogenetics
#21
REVIEW
C Süsal, C Seidl, C Schönemann, F M Heinemann, T Kauke, P Gombos, R Kelsch, W Arns, U Bauerfeind, M Hallensleben, I A Hauser, G Einecke, R Blasczyk
One of the major tasks of histocompatibility and immunogenetics laboratories is the pretransplant determination of unacceptable antigen mismatches (UAM) in kidney transplant recipients. In this procedure, human leucocyte antigen (HLA) specificities are defined against which the patient has circulating alloantibodies that are expected to harm the transplanted organ. Using the information on UAM and the potential donor's complete HLA typing, prediction of the crossmatch result, the so called 'virtual crossmatch', is possible...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26429803/identification-of-a-new-hla-a-24-allele-a-24-313
#22
JOURNAL ARTICLE
S-K Kim, H-B Oh, C E Yoon, J-H Jun
The new allele, A*24:313, showed one nucleotide difference with A*24:02:01 (595G>A).
November 2015: Tissue Antigens
https://read.qxmd.com/read/26427335/identification-of-a-novel-hla-b-46-01-variant-hla-b-46-01-20-in-a-taiwanese-unrelated-hematopoietic-stem-cell-donor
#23
JOURNAL ARTICLE
K L Yang, J H Hung, P Y Lin
One nucleotide replacement at residue 528 of HLA-B*46:01:01 results in a new allele, HLA-B*46:01:20.
November 2015: Tissue Antigens
https://read.qxmd.com/read/26423800/allelic-polymorphism-of-kir2dl2-2dl3-in-a-southern-chinese-population
#24
JOURNAL ARTICLE
J Zhen, L He, Y Xu, J Zhao, Q Yu, H Zou, G Sun, Z Deng
KIR2DL2 and KIR2DL3 segregate as alleles of the same killer cell immunoglobulin-like receptor (KIR) gene locus. They have been associated with viral infectious diseases and certain cancers and their allelic information may help to better comprehend mechanisms. The allelic polymorphism of KIR2DL2/2DL3 has been shown to influence their binding specificity and affinity to the HLA-C1 ligands. The present study aims to investigate the distribution of the allelic polymorphism of KIR2DL2/2DL3 in a southern Chinese population using sequence-specific primer polymerase chain reaction (PCR-SSP) and PCR-sequence-based typing (SBT) at the entire coding sequence...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26411515/sequence-based-typing-identification-of-a-novel-hla-a-33-95-variant-in-a-chinese-family
#25
JOURNAL ARTICLE
X-J Wang, C Han, Y Zhang, Q-H Li, K Ru
One nucleotide replacement in codon 17 (CGC>CAC) of HLA-A*33:03:01 results in a novel allele, HLA-A*33:95.
November 2015: Tissue Antigens
https://read.qxmd.com/read/26403607/characterization-of-the-novel-hla-c-08-01-09-allele-identified-in-a-chinese-han-individual
#26
JOURNAL ARTICLE
D-M Wang
HLA-C*08:01:09 allele differs from HLA-C*08:01:01 at nt735 C>T in exon 4.
November 2015: Tissue Antigens
https://read.qxmd.com/read/26403483/ctla-4-and-cd28-genes-polymorphisms-and-renal-cell-carcinoma-susceptibility-in-the-polish-population-a-prospective-study
#27
JOURNAL ARTICLE
K Tupikowski, A Partyka, A Kolodziej, J Dembowski, P Debinski, A Halon, R Zdrojowy, I Frydecka, L Karabon
Polymorphisms in co-stimulatory genes are associated with susceptibility to several malignances such as breast cancer, cervical cancer and chronic lymphocytic leukemia, but have been scarcely investigated in renal cell cancer (RCC). A total of 310 RCC patients and 518 controls were genotyped for single-nucleotide polymorphisms (SNPs) in the CTLA-4 and CD28 genes: CTLA-4c.49A>G (rs231775), CTLA-4g.319C>T (rs5742909), CTLA-4g.*6230G>A (CT60; rs3087243), CTLA-4g.*10223G>T (Jo31; rs11571302), CD28c...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26399227/two-new-hla-b35-subtypes-characterized-in-spaniards-hla-b-35-270-and-hla-b-35-273
#28
JOURNAL ARTICLE
F Sánchez-Gordo, A Pacho, A Balas, A Arrieta, J L Vicario
Two new HLA-B*35 alleles, B*35:270 and B*35:273, were characterized in the Spanish population.
November 2015: Tissue Antigens
https://read.qxmd.com/read/26396036/full-length-hla-drb1-coding-sequences-generated-by-a-hemizygous-rna-sbt-approach
#29
JOURNAL ARTICLE
K E H Gerritsen, M Groeneweg, C M H Meertens, C E M Voorter, M G J Tilanus
Currently 1582 HLA-DRB1 alleles have been identified in the IMGT/HLA database (v3.18). Among those alleles, more than 90% have incomplete allele sequences, which complicates the analysis of the functional relevance of polymorphism beyond exon 2. The polymorphic index of each individual exon of the currently known allele sequences, shows that polymorphism is present in all exons, albeit not equally abundant. Full-length HLA-DRB1 RNA sequencing identifies polymorphism of the complete coding region. Here we describe a hemizygous full-length RNA sequence-based typing (SBT) approach based on group-specific HLA-DRB1 amplification and subsequent sequencing...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26392055/a-limit-to-the-divergent-allele-advantage-model-supported-by-variable-pathogen-recognition-across-hla-drb1-allele-lineages
#30
JOURNAL ARTICLE
Q Lau, Y Yasukochi, Y Satta
Genetic diversity in human leukocyte antigen (HLA) molecules is thought to have arisen from the co-evolution between host and pathogen and maintained by balancing selection. Heterozygote advantage is a common proposed scenario for maintaining high levels of diversity in HLA genes, and extending from this, the divergent allele advantage (DAA) model suggests that individuals with more divergent HLA alleles bind and recognize a wider array of antigens. While the DAA model seems biologically suitable for driving HLA diversity, there is likely an upper threshold to the amount of sequence divergence...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26373706/study-of-association-of-ctla4-gene-variants-to-non-anterior-uveitis
#31
JOURNAL ARTICLE
D A Leon Rodriguez, A Serrano Lopera, M Cordero-Coma, A Márquez, A Fonollosa, I Ruiz-Arruza, J L Callejas, J L García Serrano, D Díaz Valle, E Pato, J Cañal, M J del Rio, M J Capella, A Blanco, J L Olea, Y Cordero, J M Martín-Villa, M B Gorroño-Echebarría, B Molins, A Adán, J Martin
This study was undertaken to investigate the possible genetic association of functional CTLA4 polymorphisms with susceptibility to non-anterior uveitis. Four hundred and seventeen patients with endogenous non-anterior uveitis and 1517 healthy controls of Spanish Caucasian origin were genotyped for the CTLA4 polymorphisms rs733618, rs5742909 and rs231775, using predesigned TaqMan(©) allele discrimination assays. PLINK software was used for the statistical analyses. No significant associations between the CTLA4 polymorphisms and susceptibility to global non-anterior uveitis were found...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26373631/plasma-soluble-tim-3-emerges-as-an-inhibitor-in-sepsis-sepsis-contrary-to-membrane-tim-3-on-monocytes
#32
JOURNAL ARTICLE
F Ren, J Li, X Jiang, K Xiao, D Zhang, Z Zhao, J Ai, C Hou, Y Jia, G Han, L Xie
Immune dysfunction is the main characteristic of sepsis. T cell Ig and mucin domain protein 3 (Tim-3) on the monocytes has been reported to promote immune homeostasis during sepsis, but the influences of plasm soluble Tim-3 (sTim-3) on the immune system during sepsis remain unknown. Here, 100 patients with different severities of sepsis (40 sepsis, 42 severe sepsis, and 18 septic shock) were enrolled in this study. The Tim-3 and human leukocyte antigen-DR (HLA-DR) on the circulating monocytes were detected using flow cytometry...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26373475/antibody-reactive-class-i-epitopes-defined-by-pairs-of-mismatched-eplets-and-self-eplets
#33
JOURNAL ARTICLE
M Resse, R Paolillo, B P Minucci, G Moccia, C Napoli
The identification of human leukocyte antigen (HLA) antibodies in the sera of candidates awaiting organ transplantation has evolved over time. This has been possible because of the introduction of more sensitive techniques and to the increasing focus on the structural aspects of the HLA epitopes. The use of the HLAMatchmaker algorithm in the analysis of positive sera and the verification of HLA ABC epitopes in the HLA Epitope Registry website provide new stimuli on the interpretation of antibody reactivity...
November 2015: Tissue Antigens
https://read.qxmd.com/read/26381049/a-novel-hla-allele-hla-drb1-13-204-detected-in-a-brazilian-unrelated-hematopoietic-stem-cell-donor
#34
JOURNAL ARTICLE
J E L Visentainer, E Nascimento, M M O Dalalio, C M Colli, R A Fabreti-Oliveira
The HLA-DRB1*13:204 allele differs from HLA*13:64 by two nucleotide substitutions at positions 181 and 189 in the exon 2.
October 2015: Tissue Antigens
https://read.qxmd.com/read/26381048/identification-of-a-novel-allele-dqb1-06-127-in-hispanic-sisters
#35
JOURNAL ARTICLE
T L Crawford, E T Weimer
Newly identified allele, HLA-DQB1*06:127, differs from DQB1*06:02:01 by the single nucleotide substitution 426C-A at codon 110 in exon 3.
October 2015: Tissue Antigens
https://read.qxmd.com/read/26381047/the-interaction-of-genetic-determinants-in-the-outcome-of-hcv-infection-evidence-for-discrete-immunological-pathways
#36
JOURNAL ARTICLE
T J Hydes, B Moesker, J A Traherne, S Ashraf, G J Alexander, B D Dimitrov, C H Woelk, J Trowsdale, S I Khakoo
Diversity within the innate and adaptive immune response to hepatitis C is important in determining spontaneous resolution (SR) and treatment response. The aim of this study was to analyze how these variables interact in combination; furthering our understanding of the mechanisms that drive successful immunological clearance. Multivariate analysis was performed on retrospectively collected data for 357 patients previously genotyped for interferon (IFN)-λ3/4, killer cell immunoglobulin (KIR), human leukocyte antigen (HLA) class I and II and tapasin...
October 2015: Tissue Antigens
https://read.qxmd.com/read/26381046/sequence-variations-of-the-locus-specific-5-untranslated-regions-of-sla-class-i-genes-and-the-development-of-a-comprehensive-genomic-dna-based-high-resolution-typing-method-for-sla-2
#37
JOURNAL ARTICLE
H Choi, M T Le, H Lee, M-K Choi, H-S Cho, S Nagasundarapandian, O-J Kwon, J-H Kim, K Seo, J-K Park, J-H Lee, C-S Ho, C Park
The genetic diversity of the major histocompatibility complex (MHC) class I molecules of pigs has not been well characterized. Therefore, the influence of MHC genetic diversity on the immune-related traits of pigs, including disease resistance and other MHC-dependent traits, is not well understood. Here, we attempted to develop an efficient method for systemic analysis of the polymorphisms in the epitope-binding region of swine leukocyte antigens (SLA) class I genes. We performed a comparative analysis of the last 92 bp of the 5' untranslated region (UTR) to the beginning of exon 4 of six SLA classical class I-related genes, SLA-1, -2, -3, -4, -5, and -9, from 36 different sequences...
October 2015: Tissue Antigens
https://read.qxmd.com/read/26381044/the-immunological-barriers-to-xenotransplantation
#38
REVIEW
M Vadori, E Cozzi
The availability of cells, tissues and organs from a non-human species such as the pig could, at least in theory, meet the demand of organs necessary for clinical transplantation. At this stage, the important goal of getting over the first year of survival has been reported for both cellular and solid organ xenotransplantation in relevant preclinical primate models. In addition, xenotransplantation is already in the clinic as shown by the broad use of animal-derived medical devices, such as bioprosthetic heart valves and biological materials used for surgical tissue repair...
October 2015: Tissue Antigens
https://read.qxmd.com/read/26332256/a-new-hla-b-39-allele-hla-b-39-01-15-discovered-in-a-taiwanese-rheumatoid-arthritis-patient
#39
JOURNAL ARTICLE
W-F Chen, T-Y Chang, C-C Chu, C-L Lin, Y-J Lee
The new allele B*39:01:15 differs from B*39:01:01 by a point mutation at position 315 (G>T) of exon 2.
October 2015: Tissue Antigens
https://read.qxmd.com/read/26332152/hla-drb1-14-84-may-have-been-derived-from-hla-drb1-14-05-and-hla-drb1-04-58-via-a-genetic-recombination-event
#40
JOURNAL ARTICLE
K L Yang, J H Hung, P Y Lin
Derivation of HLA-DRB1*14:84 via a genetic recombination event.
October 2015: Tissue Antigens
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