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PMID: 2932336 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The ability of Ia and H-2Kk-bearing membranes to replace the antigen-presenting cell in an H-2Kk allogeneic cytotoxic T cell response.

European journal of immunology ·Vol. 15 ·No. 10 ·1985-10-00 ·Pages 1013-8

Weinberger O, Herrmann SH, Greenstein JL, Mescher MF, Burakoff SJ

Abstract

Induction of an allogeneic cytotoxic T lymphocyte (CTL) response is dependent, in part, on uptake and processing of the class I alloantigen by antigen-presenting cells and subsequent Ia-restricted recognition of the alloantigen by helper T cells, resulting in lymphokine production. The nature of the antigen-processing event has been investigated using reconstituted membranes to replace the antigen-presenting cells in the generation of a secondary allogeneic CTL response. Membranes were isolated from an Iad-positive antigen presenting B cell lymphoma (D2N), detergent solubilized and then reconstituted together with affinity-purified H-2Kk antigen in the presence of protease inhibitors. These reconstituted vesicles, containing both syngeneic Ia and alloantigen, were able to induce the helper T cell arm of the CTL response in cultures depleted of antigen-presenting cells. A variety of control experiments provided strong evidence that the helper T cells recognized the H-2Kk, probably in its native form, in an Ia-restricted manner on the vesicles, while the pre-CTL can directly recognize H-2Kk. Recognition was only effective if both the Ia and alloantigen were inserted into the same membrane bilayer. The results strongly suggest that the obligatory antigen processing event required for helper T cell recognition of alloantigen is simply the insertion of the alloantigen into the same membrane bilayer as the syngeneic Ia restricting element.

MeSH Terms
Animals Antigen-Presenting Cells/immunology B-Lymphocytes/immunology Cell Membrane/immunology Cytotoxicity, Immunologic H-2 Antigens/immunology Histocompatibility Antigens Class II/immunology Lymphocyte Cooperation Mice T-Lymphocytes, Cytotoxic/immunology T-Lymphocytes, Helper-Inducer/immunology
Chemicals
H-2 Antigens Histocompatibility Antigens Class II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Weinberger O
Herrmann S H
Greenstein J L
Mescher M F
Burakoff S J
Article Info
Journal
European journal of immunology
Abbr.
Eur J Immunol
ISSN
0014-2980
Published
1985-10-00
Pages
1013-8
Language
English
Region
Germany
NLM ID
1273201
Subset
IM
Grants
NIAID NIH HHS · AI-17258 · United States
NCI NIH HHS · CA 14723 · United States
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