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PMID: 77881 Published · ppublish English Journal Article

Alloantigens determined by a second D region locus elicit a strong in vitro cytotoxic response.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 120 ·No. 6 ·1978-06-00 ·Pages 1836-40

Hansen TH, Levy RB

Abstract

The newly defined L antigen (previously designated D') has been studied with the CML assay. Balb/c-H-2db mice, which carry a loss mutation in the D region, were found to generate anti-L cytotoxic effector cells when stimulated with wild-type (BALB/c) cells. When the target cells were treated with an antiserum against L, cytolysis by BALB/c-H-2db anti-BALB/c effectors was completely blocked. However, an antiserum against D, the antigen that bears the D region private specificity, had no effect on the anti-L cytotoxic response. In a control CML experiment that was specific for the D antigen, the antiserum to L had no effect, whereas the antiserum to D blocked completely. These results indicate that the L and D antigens are recognized in a CML response as separate entities on the cell surface. In an allogeneic response to the products of the D region, cytotoxic effectors were generated that were specific for L in addition to those specific for D. This conclusion was supported by blocking experiments with either antisera or unlabeled targets. These functional studies thus extend previous co-capping and immunochemical studies, and further support the hypothesis that L is a third transplantation antigen similar to the K and D antigens.

MeSH Terms
Animals Binding, Competitive Chromosome Mapping Clone Cells Cytotoxicity, Immunologic Epitopes Immune Sera/pharmacology Isoantigens/genetics Mice Mice, Inbred BALB C Spleen/immunology
Chemicals
Epitopes Immune Sera Isoantigens
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hansen T H
Levy R B
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1978-06-00
Pages
1836-40
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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