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Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice
We have shown for the first time that it is possible to consistently generate a primary in vitro cytotoxic T cell (Tc) response to non-major histocompatibility complex alloantigens using responder cells from a normal mouse strain. This was achieved by carrying out, in the generating phase, a limitin...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1982
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186758/ https://www.ncbi.nlm.nih.gov/pubmed/6980257 |
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collection | PubMed |
description | We have shown for the first time that it is possible to consistently generate a primary in vitro cytotoxic T cell (Tc) response to non-major histocompatibility complex alloantigens using responder cells from a normal mouse strain. This was achieved by carrying out, in the generating phase, a limiting dilution procedure in which it appears that suppressor cells that inhibit Tc activation or expansion are too dilute to manifest their effect. Moreover, the response was observed in mouse serum-(MS) as well as fetal calf serum- (FCS) supplemented media, an important finding in the light of the anomalous nonspecific effects induced by FCS. The cytotoxic response produced in MS-supplemented media was shown to be highly specific in both the generating and effector phases, whereas the responses in FCS had a strong nonspecific component. |
format | Text |
id | pubmed-2186758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1982 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21867582008-04-17 Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice J Exp Med Articles We have shown for the first time that it is possible to consistently generate a primary in vitro cytotoxic T cell (Tc) response to non-major histocompatibility complex alloantigens using responder cells from a normal mouse strain. This was achieved by carrying out, in the generating phase, a limiting dilution procedure in which it appears that suppressor cells that inhibit Tc activation or expansion are too dilute to manifest their effect. Moreover, the response was observed in mouse serum-(MS) as well as fetal calf serum- (FCS) supplemented media, an important finding in the light of the anomalous nonspecific effects induced by FCS. The cytotoxic response produced in MS-supplemented media was shown to be highly specific in both the generating and effector phases, whereas the responses in FCS had a strong nonspecific component. The Rockefeller University Press 1982-08-01 /pmc/articles/PMC2186758/ /pubmed/6980257 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice |
title | Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice |
title_full | Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice |
title_fullStr | Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice |
title_full_unstemmed | Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice |
title_short | Primary in vitro cytotoxic T cell response to non-major histocompatibility complex alloantigens in normal mice |
title_sort | primary in vitro cytotoxic t cell response to non-major histocompatibility complex alloantigens in normal mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186758/ https://www.ncbi.nlm.nih.gov/pubmed/6980257 |