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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1983-2-25
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pubmed:abstractText |
Inability to develop CTL in vivo to hapten-altered self can be attributed in part to an inhibitor of interleukin 2 (IL 2) that is present in the serum of normal mice. We have shown earlier that hapten-specific CTL can be generated in C3H mice (H-2k, MIsc) provided CBA/J (H-2k MIsd) spleen cells are injected simultaneously with hapten-modified syngeneic spleen cells into the hind foot paws. In efforts to determine whether serum levels of the inhibitor of IL 2 are altered as a consequence of this successful immunization method, we have compared the activity of the inhibitor in serum at intervals after the injection of syngeneic spleen cells, CBA spleen cells, or TNP-C3H spleen cells alone or together with CBA spleen cells, by using a murine IL 2-dependent, cloned cytotoxic T cell line, CT-6. The results indicate that inhibitor was neutralized optimally 48 to 72 hr after injection of TNP-C3H spleen cells mixed with CBA/J spleen cells. The order in which neutralization occurred was as follows: TNP-C3H cells + CBA/J cells greater than CBA cells greater than TNP-C3H cells greater than normal C3H spleen cells. Furthermore, supernatants from cultures of C3H lymph node cells stimulated in vivo with CBA/J cells also contained IL 2 activity. Thus, injection of CBA/J cells with TNP-modified syngeneic spleen cells produces IL 2 in vivo in sufficient quantity to neutralize the activity of the inhibitor as well as to facilitate the maturation of pre-CTL into hapten-altered self-specific CTL.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
130
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
533-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6217243-Animals,
pubmed-meshheading:6217243-Female,
pubmed-meshheading:6217243-Haptens,
pubmed-meshheading:6217243-Immune Tolerance,
pubmed-meshheading:6217243-Interleukin-2,
pubmed-meshheading:6217243-Lymph Nodes,
pubmed-meshheading:6217243-Lymphocyte Activation,
pubmed-meshheading:6217243-Mice,
pubmed-meshheading:6217243-Mice, Inbred C3H,
pubmed-meshheading:6217243-Mice, Inbred CBA,
pubmed-meshheading:6217243-Minor Histocompatibility Loci,
pubmed-meshheading:6217243-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:6217243-T-Lymphocytes, Helper-Inducer,
pubmed-meshheading:6217243-Trinitrobenzenes
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pubmed:year |
1983
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pubmed:articleTitle |
In vivo development of cytolytic T lymphocytes (CTL) to hapten-altered self: MIs-disparate cells facilitate the response by neutralizing IL 2 inhibitor.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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