Immunochemical Study of Antigenic Specificity in Delayed Hypersensitivity
نویسندگان
چکیده
Delayed hypersensitivity in guinea pigs was produced by immunization. with a conjugate prepared by coupling diazotized arsanilic acid to polytyrosine. The resulting sensitivity could be demonstrated by skin test with conjugates prepared from a wide variety of tyrosine-containing proteins. Definite but smaller degrees of sensitivity could be induced with conjugates of proteins containing little or no tyrosine. The apparent absence of carrier-specificity is considered to be due to the narrowed range of immunologic response produced by immunization with polytyrosine-azobenzenearsonate. Injections of the hapten N-acetyltyrosine-azobenzenearsonate was found to suppress completely the delayed reaction attributable to the tyrosine-azobenzenearsonate group. The same hapten was only slightly effective in suppressing reactions in guinea pigs immunized with guinea pig serum albumin-azobenzenearsonate, suggesting that a broader range of specificities is involved with such antigens. Confirmation of such increased range of specificity attributable to antigenic determinants contributed by the carrier protein was obtained by desensitization studies with N-acetyltyrosine-azobenzenearsonate and guinea pig serum albumin-azobenzoate. While separately these materials produced only a slight decrease in skin reactivity to guinea pig serum albumin-azobenzenearsonate, the combination was found to give almost complete suppression.
منابع مشابه
Immunochemical Study of Antigenic Specificity in Delayed Hypersensitivity Iv. the Production of Unresponsiveness to Delayed Hypersensitivity with a Single Antigenic Determinant*
Immunological specificity for delayed skin reactions, as well as for circulating antibody, has been investigated with many haptens coupled to antigenic protein carriers (1). With these antigens, hapten-specific antibodies were formed consistently, whereas delayed reactions were produced only with the immunizing antigen and not with conjugates of the same hapten with a different cartier protein....
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Arsanilic acid conjugated to poorly antigenic carriers was shown to be capable of producing good hapten-specific delayed hypersensitivity but poor haptenspecific antibody production (1). This hapten-specific delayed hypersensitivity was only transiently suppressed by intravenous injections of monovalent conjugates of arsanilic acid and N-acetyltyrosine (2). On the other hand , intramuscular, in...
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Studies of immunologic specificity in delayed hypersensitivity to haptenprotein conjugates have thus far been interpreted as demonstrating that the carrier protein contributes an important component to the specificity of the reaction. I t has been suggested, for example (1), that delayed hypersensitivity represents a "broadened" specificity which becomes narrowed to more dearly defined grouping...
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ورودعنوان ژورنال:
- The Journal of Experimental Medicine
دوره 122 شماره
صفحات -
تاریخ انتشار 1962