Abstract
We have developed a procedure for immune selection in an established human lymphoid cell line based on HL-A, the major human histocompatibility locus. After a single brief exposure to selective conditions, HL-A2 variant clones were isolated from an HL-A2/HL-A3 heterozygous line. The variant clones occurred at a frequency of about 1 x 10(-6). The variant phenotype was stable during prolonged growth in the absence of antiserum after isolation. The variant sublines bound [unk] 1/1000 the HL-A2 antibody per cell as the parent line. Variation was specific in that expression of antigens not selected against was unimpaired. Loss of the chromosome bearing HL-A2 was excluded as the cause of variation because the variants, like the parent line, were heterozygous for phosphoglucomutase (EC 2.7.5.1) determined by structural locus PGM(3), which is linked to HL-A.
MeSH Terms
Animals
Binding Sites, Antibody
Cell Line
Clone Cells
Complement System Proteins
Culture Media
Cytotoxicity Tests, Immunologic
Electrophoresis, Starch Gel
Genetic Variation
Histocompatibility Antigens
Homozygote
Humans
Immune Sera
Lymphoid Tissue/enzymology,immunology
Phenotype
Phosphoglucomutase/isolation & purification
Rabbits/immunology
Selection, Genetic
Chemicals
Culture Media
Histocompatibility Antigens
Immune Sera
Complement System Proteins
Phosphoglucomutase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pious D
Hawley P
Forrest G
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16 references, click to expand
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