Center-Specific Variations in Donor Antigen Frequency: Does the OPTN cPRA Calculator Apply to Your Center?

2015 ◽  
Vol 34 (4) ◽  
pp. S169 ◽  
Author(s):  
S.A. Hollander ◽  
D.B. Tyan ◽  
M. Fernandez-Vina ◽  
D. Bernstein ◽  
N. McDonald ◽  
...  
Keyword(s):  
Blood ◽  
1997 ◽  
Vol 89 (3) ◽  
pp. 1027-1034 ◽  
Author(s):  
Juergen Bux ◽  
Ernst-Ludwig Stein ◽  
Philippe Bierling ◽  
Patricia Fromont ◽  
Mary Clay ◽  
...  

Abstract Polymorphic structures of the neutrophil Fcγreceptor IIIb (FcγRIIIb) result in alloantibody formation that causes alloimmune neonatal neutropenia and transfusion reactions. Alloantigens located on FcγRIIIb include the antigens NA1 and NA2. In four cases of alloimmune neonatal neutropenia, granulocyte-specific alloantibodies directed against a thus far unknown antigen were detected by granulocyte agglutination and immunofluorescence tests in the maternal sera. By the use of the monoclonal antibody–specific immobilization of granulocyte antigens (MAIGA) assay, the new antigen, termed SH, was located on the FcγRIIIb. Nucleotide sequence analysis of the FcγRIIIb coding region from a SH(+) individual showed a single-base C→A mutation at position 266, which results in an Ala78Asp amino acid substitution. A family study confirmed that this nucleotide difference is inherited, and corresponds to the SH phenotype. Serologic typing of 309 randomly selected individuals showed an antigen frequency of 5% in the white population. The same frequency was found by genotyping, for which a technique based on polymerase chain reaction (PCR) using sequence-specific primers (PCR-SSP) was developed. Typing of all SH(+) individuals for NA1 and NA2, and PCR-restriction fragment length polymorphism analysis of the NA-specific PCR products from five SH(+) individuals using the SH-specific endonuclease SfaN I showed that SH antigen is very probably the result of an additional mutational event in the NA2 form of the FcγRIIIB gene. Immunochemical studies also demonstrated that the SH determinants reside on the 65- to 80-kD NA2 isoform of the FcγRIIIb. Our findings show the existence of an additional polymorphism of the FcγRIIIb, which can result in alloantibody formation causing alloimmune neonatal neutropenia.


2015 ◽  
Vol 40 (3) ◽  
pp. 102-106 ◽  
Author(s):  
A Nessa ◽  
S Tabassum ◽  
S Sultana

Human leukocyte antigen B27 (HLA-B27), a class I molecules of the major histocompatibility complex has a strong disease association with different types of spondarthropathies (SpA). The strength of this disease association varies markedly among racial and ethnic populations. The present study aimed to identify the HLA-B27 antigen frequencies among suspected SpA patients as well as healthy Bangladeshi individuals. The frequency of HLA-B27 was determined in 1500 patients and 1000 healthy subjects attending the Bangabandhu Sheikh Mujib Medical University (BSMMU). HLAB 27 typing was done by microlymphocytotoxicity test using commercial kit. A total of 738 (49.2%) suspected SpA patients and 107 (10.7%) healthy subjects tested positive for HLA-B27 antigen with higher frequency among younger age groups (54.9%, 52.4% and 56.2% in 0-14 years, 15-24 years and 25–34 years of age respectively). The male female positivity was almost same (11.4% and 9.6%) among control group, but in patient group it was 53.0% and 41.2% respectively. The findings of this hospital based study showed a high frequency of HLA-B27 among suspected SpA patients with male preponderance which is comparable with neighboring countries.Bangladesh Med Res Counc Bull 2014; 40 (3): 102-106


2003 ◽  
Vol 170 (4 Part 1) ◽  
pp. 1443-1446 ◽  
Author(s):  
EKKEHARD W. HAUCK ◽  
ARNE HAUPTMANN ◽  
WOLFGANG WEIDNER ◽  
GREGOR BEIN ◽  
HOLGER HACKSTEIN

1972 ◽  
Vol 287 (15) ◽  
pp. 740-743 ◽  
Author(s):  
Seymour H. White ◽  
Victor D. Newcomer ◽  
Max R. Mickey ◽  
Paul I. Terasaki
Keyword(s):  

2008 ◽  
Vol 25 (3) ◽  
pp. 156-162 ◽  
Author(s):  
Kirtikant V. Sheth ◽  
Jacqueline A. Edwards ◽  
John T. Godwin

Author(s):  
A. I. Zheltikov ◽  
D. S. Adushinov ◽  
O. A. Zaiko ◽  
V. N. Dementiev ◽  
V. G. Marenkov ◽  
...  

The paper characterizes 52 producers of red steppe, 49 - red Danish and 169 Angler bulls of “Barnaulskoye” enterprise in terms of erythrocyte antigen occurrence. The authors used 53 antiserums in order to determine erythrocytic antigens of 9 genetic systems. The highest frequency observed was F antigen frequency equal to 0.976-1.000. This gene was not observed in one servicing red steppe bull and four servicing Angler bulls. All red Danish bulls had F allele in a homo- or heterozygous state. The concentration of antigens A2, B2, O1, Y2, G’, Q’ (system B), C1, C2, E, R2, W, X2 (system C), H’ (system S) in the red bulls was high and equal to 0.249-0.592. The frequency of erythrocytic antigens B1, I1, P2, T1, T2, Y1, I’, D’, J2’, P1’, B” (B), R1 (C), J (J), S2, U and H” (S) was the lowest at 0-0.122. All 53 blood factors were observed in Angler cattle, but no antigens B1, P2, R1, U и B1, Y1, B” were observed in the red steppe and red Danish cattle. There are no significant differences observed in genetic similarity among three red breeds; the index of genetic similarity are 0.9211-0.9307, which indicates a high relationship among them. The highest number of ejaculates and native sperm was obtained from Angler servicing bulls, the excess over other breeds was 11.9-13.9 and 15.1-42.8%. Red steppe bulls were characterized by lowest amount of ejaculate and less bioproducts for cryopreservation were received from them. The total breeding efficiency of cows with red steppe bull sperm was 85.1%, the superiority over Danish and Angler red cattle was 7.1-11.5%.


1991 ◽  
Vol 4 (5 Pt 1) ◽  
pp. 393-398 ◽  
Author(s):  
B. I. Freedman ◽  
M. A. Espeland ◽  
E. R. Heise ◽  
P. L. Adams ◽  
V. M. Buckalew ◽  
...  

1983 ◽  
Vol 62 (2) ◽  
pp. 147-150 ◽  
Author(s):  
S. S. Papiha ◽  
J. Wentzel ◽  
D. F. Roberts ◽  
Y. Subba Rao ◽  
C. M. Habibullah

2008 ◽  
Vol 10 (4) ◽  
pp. 303-305 ◽  
Author(s):  
Ammar A. R. Jabbar ◽  
Heather M. Dick

2018 ◽  
Vol 44 (1) ◽  
pp. 1-8
Author(s):  
Sharmin Sultana ◽  
Shahina Tabassum ◽  
Afzalun Nessa

Human leukocyte antigen (HLA) are cell surface glycoproteins encoded by Major Histocompatibility Complex (MHC) geneof human genome. HLA antigen frequency and haplotype distribution are useful for determining disease associations, origin, migration and genetic relationships between populations and predicting the outcome of transplantation. Thus, the present study was carried outto identify HLA class I (HLA-A and HLA-B) antigen and haplotype distribution among a selected Bangladeshi population. This retrospective study was conducted among 1070 individuals who were referred by cliniciansfor HLA typing at the Tissue Typing Laboratory of the Department of Virology, Bangabandhu Sheikh Mujib Medical University (BSMMU) during the period 2009 to 2011. For HLA typing, Blood was collected in heparin containing tube and the laboratory tests were performed by the microlymphocytotoxicity technique according to manufacturer’s instructions.Out of 19 HLA-A and 37HLA-B antigens tested, a total of 19/19 and 36/37 antigens were detectedrespectively in this study. The most frequent antigens of HLA-A and HLA-B detected were A11 (25.4%), A24 (16.6%), B75 (18.1%) and B35 (11.3%). The least antigen frequency detected for HLA-A locus were A69 (0.09%), A26 (0.28%), A34 (0.28%), while for HLA-B locus were B81 (0.09%) and B56 (0.09%). Among the HLA-A and HLA-B antigens, some alleles were found to be homozygote such as A11 (4.0%), A2 (2.7%), A24 (2.1%) andB75 (2.4%), B35 (1.8%), and B44 (1.4%) respectively. The most frequent haplotype in the study populationwereA11: B75 (4.9%). The most frequent antigens of HLA-A and HLA-B detected were A11 (25.4%), B75 (18.1%) respectively. The distribution of HLA haplotypes among the study population indicates that it has the influence of Oriental and Asian populations. Thus, this study will be helpful to provide valuable information for population genetics and HLA disease association analysis.Bangladesh Med Res Counc Bull 2018; 44(1):01-08


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