Abstract
This paper describes the specificity of AKR anti-(a) [AKR anti-trinitrophenylated AKR (AKR-TNP)] [AKRa (AKRaAKR TNP)] antisera raised in syngeneic AKR mice against AKRaAKR-TNP cell populations enriched for H-2-restricted aTNP cytotoxic lymphocytes (CTL) by blast-cell isolation. The activity of the antisera resided in the Ig fraction. All antisera were shown to reproducibly react with AKRaAKR-TNP-CTL-containing cell populations in indirect immunofluorescence and all removed the major fraction of CTL in complement-dependent lysis causing a considerable depression of cell-mediated lympholysis. The antisera were nonreactive with alloreactive AKRaC57BL/6 CTL and other H-2-restricted AKR CTL against fluorescein-isothiocyanate-conjugated AKR-target cells. It could be excluded that the antisera contained contaminating antibodies against TNP, TNP-neoantigenic determinants (NAD), or processed CTL-receptor-bound TNP-NAD, thus demonstrating specificity for determinants on T cell receptors of AKRaAKR-TNP CTL. These receptors were produced by the CTL themselves. These observations are interpreted to suggest that AKRa (AKRaAKR-TNP) antisera contain anti-idiotypic antibodies directed against specificity-associated determinants (idiotypes) on T cell receptors of H-2-restricted AKRaAKR-TNP CTL. The antisera provide a new tool to study the genetic control of idiotype expression on H-2-restricted CTL, the biochemistry of T cell receptors, and the regulation of the generation of H-2 restricted CTL on the idiotype level.
MeSH Terms
Animals
Antibodies, Anti-Idiotypic
Antibody Specificity
Antigens, Surface
Cytotoxicity, Immunologic
Epitopes
H-2 Antigens
Immunoglobulin Idiotypes
Major Histocompatibility Complex
Mice
Mice, Inbred AKR/immunology
Receptors, Immunologic/immunology
T-Lymphocytes/immunology
Trinitrobenzenes/immunology
Chemicals
Antibodies, Anti-Idiotypic
Antigens, Surface
Epitopes
H-2 Antigens
Immunoglobulin Idiotypes
Receptors, Immunologic
Trinitrobenzenes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Krammer P H
Rehberger R
Eichmann K
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