The Behavior of Hapten-poly-l-lysine Conjugates as Complete Antigens in Genetic Responder and as Haptens in Nonresponder Guinea Pigs

نویسندگان

  • Ira Green
  • William E. Paul
  • Baruj Benacerraf
چکیده

30 to 40% of Hartley strain guinea pigs have previously been demonstrated to possess a dominant autosomal gene which enables them to recognize the antigenicity of hapten-poly-L-lysine conjugates as expressed by the development of both antihapten antibodies and delayed hypersensitivity to the immunizing antigen. In the present study, it was shown that PLL alone was weakly antigenic in such genetic responder animals. Immunization with DNP-PLL electrostatically combined with foreign albumins elicits the production of anti-DNP antibodies in all Hartley strain guinea pigs, although the percentage of animals demonstrating a delayed response to DNP-PLL and therefore considered genetic responders remains 30 to 40%. Immunization with nonantigenic polyanions combined with DNP-PLL does not produce such an effect. Some degree of PLL specificity of purified anti-DNP antibodies produced by genetic nonresponder animals by immunization with DNP-PLL combined with foreign albumins was demonstrated by means of fluorescence quenching.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Hapten-carrier relationships.

The ability of guinea pigs to recognize poly-I,-lysine (PLL), and hapten conjugates of PLL (H-PLL) as antigens is under the control of a single autosomal dominant gene which we will refer to as the PLL gene (1-3). Responder animals carrying this gene form specific antihapten antibodies and display delayed hypersensitivity reactions after immunization with H-PLL conjugates such as 2,4-dinitrophe...

متن کامل

T H E Behavior of Hapten-poly-l-lysine Conjugates as Complete Antigens in Genetic Responder and as Haptens in Nonresponder Guinea Pigs* by Ira Green,$ M.d., William E. Paul,§ M.d., Ai~d

About 30 to 40 % of random bred Hartley strain (1) and all strain 2 guinea pigs (2) recognize hapten-poly-I.-lysine conjugates (H-PLL) as antigens. Strain 13 guinea pigs (2), mice, rats, and rabbits (3) do not make an immune response to these compounds. The immune response of guinea pigs to H-PLL conjugates has been shown to" be controlled by a dominant autosomal gene (2, 4). Contrasting with t...

متن کامل

STUDIES ON ANTIGENICITY THE RELATIONSHIP BETWEEN IN VIvo AND IN VITRO ENZYMATIC DEGRADABILITY OF HAPTEN-POLYLYSINE CONJUGATES AND THEIR ANTIGENICITIES IN GUINEA PIGS*

tIapten conjugates of synthetic poly amino adds are useful tools for the investigation of the metabolism of antigen, which is an early step in the immune response. Previous studies have shown that approximately 25 per cent of random-bred guinea pigs and 100 per cent of the highly inbred strain 2 guinea pigs are capable of developing an immune response to lightly coupled hapten-poly-L-lysine (PL...

متن کامل

STUDIES ON ARTIFICIAL ANTIGENS III. THE GENETIC CONTROL OF Tile IMMUNE RESPONSE TO HAPTEN- POLY-L-LYSINE CONJUGATES IN GUINEA

Previous studies on the genetic transmission of the capacity for an immune response have shown that there is a statistically significant relation between the abilities of parents and of offspring to respond to a given antigen (1-3). Mendelian genetic patterns were not observed, however, possibly because of the structural complexity of the immunizing antigens employed. Poly-L-aamino acids and ha...

متن کامل

Studies on Antigenicity

The enzymatic degradation of fluorescein conjugates of poly-L-lysine, poly-D-lysine, and exhaustively succinylated poly-L-lysine by aqueous extracts of spleens from "responder" (guinea pigs which can develop immune responses to hapten-poly-L-lysine conjugates) and "non-responder" guinea pigs was investigated. The in vivo degradation of H(3)-tagged dinitrophenyl conjugates of these synthetic pol...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of Experimental Medicine

دوره 123  شماره 

صفحات  -

تاریخ انتشار 1966