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PMID: 9537038 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Long-term maintenance of HLA-D restricted T cells specific for soluble antigens.

Scandinavian journal of immunology ·Vol. 11 ·No. 2 ·1980-00-00 ·Pages 131-6

Kurnick JT, Altevogt P, Lindblom J, Sjöberg O, Danneus A, Wigzell H

Abstract

Lymphocytes from donors sensitized to soluble protein antigens tuberculin (PPD) and tetanus toxoid were stimulated in vitro with these antigens. The blasts were isolated on density gradients and maintained in long-term proliferating culture by the addition of supernatants from phytohaemagglutinin-stimulated (PHA) cultures. Blasts can be shown to retain specificity for the original stimulating antigen as measured by stimulation of DNA synthesis, but only when the antigen is presented in the company of a cooperating cell population. Autologous irradiated peripheral blood lymphocytes provide the best cooperation, but donors who share HLA-D antigens will also allow for continued proliferation in the presence of the appropriate soluble antigen. Donors sharing at HLA-A, -B, or -C show minimal ability to cooperate. The soluble antigen-specific blast cells do not manifest alloreactivity. The data are discussed with regard to possible application to clinical histocompatibility typing and to the implications of selfrecognition in the immune response.

MeSH Terms
Cell Division Cells, Cultured Culture Media HLA-D Antigens/immunology Humans Lymphocyte Activation Lymphocyte Cooperation Mitogens/pharmacology T-Lymphocytes/cytology Tetanus Toxoid/immunology
Chemicals
Culture Media HLA-D Antigens Mitogens Tetanus Toxoid
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kurnick J T
Department of Immunology, Uppsala University, Sweden.
Altevogt P
Lindblom J
Sjöberg O
Danneus A
Wigzell H
Article Info
Journal
Scandinavian journal of immunology
Abbr.
Scand J Immunol
ISSN
0300-9475
Published
1980-00-00
Pages
131-6
Language
English
Region
England
NLM ID
0323767
Subset
IM
Grants
NIAID NIH HHS · 1 F 32-AI-5479-01 · United States
NCI NIH HHS · CB-74129-31 · United States
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