Freeze-thaw-refreeze cycle to prepare lymphocytes for HLA antibody detection or tissue typing
Identifieur interne : 000D24 ( Istex/Corpus ); précédent : 000D23; suivant : 000D25Freeze-thaw-refreeze cycle to prepare lymphocytes for HLA antibody detection or tissue typing
Auteurs : Paul NathanSource :
- Cryobiology [ 0011-2240 ] ; 1974.
Abstract
Human lymphocytes stored in the frozen state may be thawed, placed on cytotoxicity plates, refrozen, rethawed and used for screening sera or tissue-typing of the cells. The simple procedure described uses only a −90 °C refrigerator for both freezing and storage of the cells. The technique permits a laboratory to collect a variety of cells over a long period, so that a set of test plates with cells from 10 to 20 donors can be prepared when a convenient number of donor cells are available. Also, the refrozen cells in cytotoxicity test plates may be warmed to the temperature of dry ice for 24 hr, returned to the refrigerator set at a slightly lower temperature, and at a later time, these cells may be thawed and used for serum screening. In view of these results, it appears possible to ship the refrozen cells from one laboratory to another using simple dry ice storage during the transfer. Negative reactions due to soluble antigens in the suspending sera can be obviated by washing out these sera and replacing them with medium 199 or alternatively, fetal calf serum can be used to replace the human serum in the suspending media.
Url:
DOI: 10.1016/0011-2240(74)90006-6
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The simple procedure described uses only a −90 °C refrigerator for both freezing and storage of the cells. The technique permits a laboratory to collect a variety of cells over a long period, so that a set of test plates with cells from 10 to 20 donors can be prepared when a convenient number of donor cells are available. Also, the refrozen cells in cytotoxicity test plates may be warmed to the temperature of dry ice for 24 hr, returned to the refrigerator set at a slightly lower temperature, and at a later time, these cells may be thawed and used for serum screening. In view of these results, it appears possible to ship the refrozen cells from one laboratory to another using simple dry ice storage during the transfer. Negative reactions due to soluble antigens in the suspending sera can be obviated by washing out these sera and replacing them with medium 199 or alternatively, fetal calf serum can be used to replace the human serum in the suspending media.</div></front></TEI><istex><corpusName>elsevier</corpusName><author><json:item><name>Paul Nathan</name><affiliations><json:string>Shriners Burns Institute, Cincinnati Unit, Cincinnati, Ohio 45219 USA</json:string><json:string>Departments of Physiology and Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio 45219 USA</json:string></affiliations></json:item></author><language><json:string>eng</json:string></language><abstract>Human lymphocytes stored in the frozen state may be thawed, placed on cytotoxicity plates, refrozen, rethawed and used for screening sera or tissue-typing of the cells. The simple procedure described uses only a −90 °C refrigerator for both freezing and storage of the cells. 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The simple procedure described uses only a −90 °C refrigerator for both freezing and storage of the cells. The technique permits a laboratory to collect a variety of cells over a long period, so that a set of test plates with cells from 10 to 20 donors can be prepared when a convenient number of donor cells are available. Also, the refrozen cells in cytotoxicity test plates may be warmed to the temperature of dry ice for 24 hr, returned to the refrigerator set at a slightly lower temperature, and at a later time, these cells may be thawed and used for serum screening. In view of these results, it appears possible to ship the refrozen cells from one laboratory to another using simple dry ice storage during the transfer. 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