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PMID: 7263311 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

HLA-A2 as a target for cell-mediated lympholysis: evidence from immunoselected HLA-A2 negative mutant cell lines.

Human immunology ·Vol. 1 ·No. 1 ·1980-07-00 ·Pages 77-86

Andreotti PE, Apgar JR, Cresswell P

Abstract

Cloned mutants of the human B lymphoblastoid cell line SB have been isolated using mutagenesis with ethyl methanesulfonate followed by negative selection with an anti-HLA-A2 serum and complement. Absorption analysis with 125I Staphylococcus aureus protein A binding to antibody sensitized cells. HLA typing, and immune precipitation analysis showed the mutants to be serologically identical to the SB parent except for the loss of HLA-A2. When tested as target cells for cell-mediated lympholysis by cytotoxic T lymphocytes generated in the mixed lymphocyte response, the SB and mutant cell lines demonstrated comparable susceptibility when the putative targets were HLA antigens other than HLA-A2. However, when compared for susceptibility to lysis by cytotoxic T lymphocytes considered to be HLA-A2 specific, the SB parent was effectively killed whereas little or no killing of the HLA-A2 mutants was observed. The results provide a new line of evidence that HLA antigens recognized by antibody can also be the true molecular targets for cytotoxic T lymphocytes.

MeSH Terms
Absorption Animals Binding Sites, Antibody Cell Line Chemical Precipitation Cytotoxicity, Immunologic HLA Antigens/immunology Histocompatibility Testing Humans Immunity, Cellular Mutation Rabbits Staphylococcal Protein A/metabolism
Chemicals
HLA Antigens Staphylococcal Protein A
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Andreotti P E
Apgar J R
Cresswell P
Article Info
Journal
Human immunology
Abbr.
Hum Immunol
ISSN
0198-8859
Published
1980-07-00
Pages
77-86
Language
English
Region
United States
NLM ID
8010936
Subset
IM
Grants
NIAID NIH HHS · AI-08897 · United States
NIAID NIH HHS · AI-14016 · United States
NIGMS NIH HHS · GM-02007 · United States
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