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[The Identification Idea of Antibodies Against Ku and Other High-Frequency Antigens].
Zhang, Fei-Fei; Li, Jing-Wei; Shen, Wei; He, Yi; Yuan, Hong; Tian, Li; Ye, Zhi-Jun.
Afiliação
  • Zhang FF; Department of Blood Transfusion, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, Sichuan Province, China.
  • Li JW; Department of Blood Transfusion, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, Sichuan Province, China.
  • Shen W; Shanghai Blood Center, Shanghai 200051, China.
  • He Y; Department of Blood Transfusion, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, Sichuan Province, China.
  • Yuan H; Department of Blood Transfusion, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, Sichuan Province, China.
  • Tian L; Institute of Blood Transfusion, Chinese Academy of Medical Science, Chengdu 610052, Sichuan Province, China.E-mail: 241775291@qq.com.
  • Ye ZJ; Department of Nutritional, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, Sichuan Province, China.E-mail:65959728@qq.com.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 32(3): 875-882, 2024 Jun.
Article em Zh | MEDLINE | ID: mdl-38926983
ABSTRACT

OBJECTIVE:

This study was aimed to provide ideas for identifying the antibodies to high-frequency antigens by analyzing a female case of high-frequency antigen antibody (anti-Ku) using serological and sequencing method.

METHODS:

The methods for identification of blood group, erythrocyte antigen, screening and identification of antibody were used to detect the blood type and antibody in the proband. The proband's serum and reagent screening cells treated with Sulfhydryl reagent were applied to judge the type and characteristics of this antibodies when reacted with the regaent screening cells or proband's serum respectively. Gene sequencing was used to determine the genotype of the proband's blood group.

RESULTS:

The proband's red blood cells were determined as O type RhD positive, whose serum showed strong positive reaction to antibody-screening cells and antibody identification cells with the same intensity in saline and IAT medium, however, the self-cells showed negative effect. The Direct Antihuman Globulin of proband's red blood cells also showed weak positive reaction, and the other blood types were CcEe, Jk(a+b-), P1-, Le(a-b -), Lu (a-b +), K-, k-, Kp(a-b-). Serum of the proband treated with 2-ME still react with three groups of screening cells in IAT medium. The reaction intensity of proband's serum was also unchanged with the cells modified with papain and bromelain, but showed negative effect when the cells were treated with sulfhydryl agents including DTT and 2-ME. Gene sequencing revealed that the KEL genotype of the patient was KEL*02N.24 . This patient had a rare K0 phenotype.

CONCLUSION:

The rare Kell-null blood group (also known as K0) were identified by serological and molecular tests in the proband who produced both IgG and IgM type of antibody to high-frequency antigen (anti-Ku). These two methods are of great significance in the identification of this rare blood group as well as the antibody to high frequency antigen.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eritrócitos Limite: Female / Humans Idioma: Zh Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eritrócitos Limite: Female / Humans Idioma: Zh Ano de publicação: 2024 Tipo de documento: Article